PUBLIKÁCIÓS JEGYZÉK

(2010. szeptember 27.)

Dr. Márton Ildikó Judit

CIKKEK

IF

A kandidátusi fokozat megszerzése előtt megjelent cikkek:

1. Harmati S, Márton I: Immunglobulinszintek vizsgálata krónikus periapikális

elváltozásokban.

Fogorv Szle 78:161-165, 1985.

2. Márton I, Harmati S, Kiss C: Komplementszint és T- lymphocytaszám

meghatározása krónikus periapikális granulómás betegekben.

Fogorv Szle 80:295-298, 1987.

3. Márton I, Harmati S, Kiss C: Immunologische Veranderungen bei Patienten mit

periapikalem Granulom.

Z Stomatol 84:93-99, 1987.

4. Márton I, Rédai I, Kelentey B, Lázár Sz, Ölveti É: Granuloma periapikális fogak

gyökércsatornabennékének mikrobiológiai vizsgálata.

Fogorv Szle 81:245-248, 1988.

A közleményt a Magyar Fogorvosok Egyesülete „ Körmöczy” díjjal jutalmazta

5. Márton I, Kiss C, Balla G, Szabó T, Karmazsin L: Acute Phase Proteins in Patients

with Chronic Periapical Granoluma before and after Surgical Treatment.

Oral Microbiol Immunol 3:95-96, 1988. IF:1.246

6. Márton I, Melczer K, Kiss C, Ilyés I: Congenitalis hypophosphatasia, mint a korai

tejfogvesztés lehetséges kóroka.

Fogorv Szle 82:49-51, 1989.

7. Márton I, Sipka S, Harmati S, Kiss C: Chemilumineszenz im Vollblut bei Patienten

mit periapikalem Granulom.

Z Stomatol 86: 191-195, 1989.

8. Márton I, Mórocz I: Periapikális granulómák szövettani vizsgálata.

Fogorv Szle 82:365-368, 1989.

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9. Márton I, Nemes Z, Harmati S: Quantitative Significance of IgE producing Plasma

Cells and Tissue Distribution of Mast Cells in Apical Periodontitis.

Oral Microbiol Immunol 5:46-48, 1990. IF:1.246

10. Márton I, Kiss C, Szabó T: Akut-fázis fehérjék szerepe a krónikus periapikális

granuloma pathogenezisében.

Fogorv Szle 83:235-239, 1990.

A kandidátusi fokozat megszerzését követően megjelent és közlésre elfogadott cikkek:

11. Márton IJ, Kiss C: Influence of Surgical Treatment of Periapical Lesions on Serum

and Blood Levels of Inflammatory Mediators.

Int Endod J 25:229-233, 1992. IF:0.253

12. Márton IJ, Kiss C: Characterization of Inflammatory Cell Infiltrate in Dental

Periapical Lesions.

Int Endod J 26:131-136, 1993. IF:0.198

13. Márton IJ, Balla G, Hegedűs C, Redl P, Szilágyi Z, Karmazsin L, Kiss C: The Role

of Reactive Oxygen Intermediates in the Pathogenesis of Chronic Apical

Periodontitis.

Oral Microbiol Immunol 8:254-257, 1993. IF:1.475

14. Nagy G, Zeher M, Madléna M, Márton I, Czirják L: A poliszisztémás autoimmun

betegségek orofaciális vonatkozásai.

Lege Artis Med 5:971-975, 1995.

15. Márton I, Bágyi K, Radics T, Kiss C: Az apicalis periodontitis kialakulása és

szervezetre gyakorolt hatása

Fogorv Szle 91:269-274, 1998.

16. Márton IJ, Dezső B, Radics T, Kiss C: Distribution of interleukin-2 receptor -

chain and cells expressing major histocompatibility complex class II antigen in

chronic human periapical lesions.

Oral Microbiol Immunol 13:259-262, 1998. IF:1.347

17. Mikala G, Xie J, Berencsi G, Kiss C, Márton I, Domján G, Vályi-Nagy I:Human

Herpesvirus 8 in Hematologic Diseases.

Pathology Oncology Research 5:73-39, 1999. IF:1.162

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18. Tar I, Bágyi K, Radics T, Márton I: Odontogén gócszűrésre beutalt betegek

vizsgálata.

Fogorv Szle 92:295-300, 1999.

19. Márton I, Radics T, Szakáll Sz, Kiss C: A sejtes összetétel, az aktivált állapotú

sejtek vizsgálata granuloma apicaleban.

Fogorv Szle 92:379-385, 1999.

20. Toida M, Márton I, Dobó Nagy C, Angyal J, Kiss Á, Kovács Gy, Redl P, Sárváry

A, Szűcs S, Balázs M, Ádány R, Tatematsu N, Keszthelyi G: Dentistry and Oral

Surgery in Hungary A Bief Report and Introduction of Institute of Dentistry,

University Medical School of Debrecen.

Hosp Dent (Tokyo) 12:131-134, 2000.

21. Márton IJ, Rot A, Schwarzinger E, Szakáll Sz, Radics T, Vályi-Nagy I, Kiss C:

Differential in situ distribution of IL-8, MCP-1 and Rantes factor in human chronic

periapical granuloma.

Oral Microbiol Immunol 15:63-65, 2000. IF:1.419

22. Márton IJ, Kiss C: Protective and destructive reaction in apical periodontitis.

Oral Microbiol Immunol 15:139-150, 2000. IF:1.419

23. Radics T, Tar I, Bágyi K, Márton I: A periapikális léziók típusainak prevalenciája, a

szövettani értékelés jelentősége.

Fogorv Szle 93:108-114, 2000.

24. Hegedűs C, Flóra-Nagy E, Martos R, Juhász A, Fülöp I, Pomaházi S, Nagy IP, Tóth

Z, Márton I, Keszhelyi G: Simplified 3D reconstruction based on hard tissue

microtome cross section pictures in dentistry.

Computer Methods and Programs in Biomedicine 63:77-84, 2000. IF:0.581

25. Márton I, Johnson SE, Damjanov I, Currie KS, Sundberg JP, Knowles B:

Expression and immune recognition of SV40 Tag in transgenic mice that develop

SV40 Tag-induced metastaic osteosarcomas.

Transgenic Res 9:115-125, 2000. IF:2.132

26. Redl P, Gyulaházi J, Kiss C, Márton I: Fibromatosis in the paramandibular region

Med Pediatr Oncol 37:75-76, 2001. IF:1.114

27. Juhász A, Szabó Z, Márton I, Fejérdy P, Dobó Nagy Cs: A gyökércsatorna

morfológiai hatása a mikroszivárgás mértékére.

Fogorv Szle 95: 27-31, 2002

4

28. Alberth M, Török J, Nemes J, Kiss C, Márton I: Antineoplastikus terápia okozta

zománcszerkezeti rendellenesség. Esetismertetés.

Fogorv Szle 95:189-193, 2002.

29. Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the involved teeth.

Oral Microbiol Immunol 18:9-13, 2003. IF:1.242

Az MTA doktora fokozat megszerzése után megjelent cikkek:

30. Alberth M, Kovalecz G, Török J, Nemes J, Kiss C, Marton IJ: Oral health of long-

term childhood cancer survivors.

Pediatr Blood Cancer (Med Pediatric Oncol) 43: 88-90, 2004. IF:1.362

31. Márton IJ, Bergenholtz G: The periapical inflammatory process-systemic and local

manifestations: introduction.

Endodontic Topics 8:1-2, 2004.

32. Márton IJ: How does the periapical inflammatory process compromise general

health?

Endodontic Topics 8:3-14, 2004.

33. Szládek G, Juhász A, Kardos G, Szőke K, Major T, Sziklai I, Tar I, Márton I,

Konya J, Gergely L, Szarka K: High co-prevalence of genogroup 1 TT virus and

human papillomavirus associated with poor clinical outcome of laryngeal carcinoma.

J Clin Pathol 58:402-405, 2005. IF: 2.170

34. Nemes JA, Nemes Z, Márton IJ: P21WAF1/CIP1

Expression is a Marker of Poor

Prognosis in Oral Squamous Cell Carcinoma.

J Oral Pathol Med 34: 274-279, 2005. IF:1.661

35. Dr. Márton Ildikó: Gócszemlélet a XXI. Században-Fogászati gyulladások és

kardiovaszkuláris betegségek lehetséges összefüggése.

Háziorvosi Továbbképző Szemle 10:379-381, 2005.

36. Nemes JA, Deli L, Nemes Z, Márton IJ: Expression of p 16INK4A

, p53, and Rb

proteins are independent from the presence of human papillomavirus genes in oral

squamous cell carcinoma.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod 102: 344-352, 2006. IF:1.221

37. Alberth M, Majoros L, Kovalecz G, Szegedi I, Márton I, Kiss C: Significance of

oral Candida infections in Children with cancer.

Pathol Oncol Res 12: 237-241, 2006. IF:1.241

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38. Bágyi K, Klekner Á, Hutóczki G, Márton I: A szájüregi baktériumok szerepe az

aspirációs pneumónia patogenezisében.

Fogorv Szle 99:205-212, 2006.

39. Nemes J, Redl P, Boda R, Márton I: Szájüregi laphámrákok vizsgálata I.

(demográfiai jellemzők, kliniko-pathológiai paraméterek, kezelés, recidíva, túlélés)

Fogorv Szle 99: 161-167, 2006.

40. Nemes J, Boda R, Redl P, Márton I: Szájüregi laphámrákok vizsgálata II. (etiológiai

faktorok)

Fogorv Szle 99:179-185, 2006.

41. Dr. Márton Ildikó: Szájüregi gyulladásos állapotok és szisztémás betegségek

kapcsolata.

Focus Medicinae VIII:21-24, 2006.

42. Vitályos G, Török J, Márton I, Szepesi M, Radics T, Hegedűs Cs: Allergiás betegek

fogszabályozó kezelésének lehetőségei (Esetismertetés).

Fogorv Szle 100:71-76, 2007.

43. Bakó J, Szepesi M, Márton I, Borbély J, Hegedűs Cs: Fogászatban alkalmazható

hatóanyagok leadására alkalmas nanorészecskék szintézise.

Fogorv. Szle 100:109-113, 2007.

44. Szabó A, Szentandrássy N, Birinyi P, Horváth B, Szabó G, Bányász T, Márton I,

Nánási P, Magyar J: Effect of articaine on action potential characteristics and the

undelying ion currents in canine ventricular myocytes.

British J Anaesthesia 99:726-733, 2007. IF: 2.948

45. Márton I: A granuloma apicale fogorvosi és általános orvostudományi jelentősége.

Fogorv. Szle 100:193-199, 2007.

46. Márton IJ: The influence of chronic apical periodontitis on oral and general health.

Fogorv. Szle 100:200-209, 2007.

47. Bágyi K, Márton I, Szabó J, Andrási M, Gáspár A, Varga I, Bognár L, Klekner Á:

Efficacy of pre-operative cephalosporin prophylaxis in controlling pathogenic oral

bacterial growth in comatose patients.

J Med Microbiol 57:128-129, 2008. IF: 2.190

48. Tar I, Kiss C, Marodi L, Márton IJ: Oral and dental conditions of children with

selective IgA deficiency.

Pediatric Allerg Immunol 19:33-36, 2008. IF: 2.723

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49. Dr. Martos Renáta, Dr. Márton Ildikó: A fogeredetű gyulladásos kórképek és a

cardiovascularis megbetegedések összefüggései (Irodalmi áttekintés)

Fogorv Szle 101: 101-105, 2008.

50. Nemes JA, Redl P, Boda R, Kiss C, Marton IJ: Oral cancer report from North

Eastren Hungary.

Pathol Oncol Res 14:85-92, 2008. IF: 1.260

51. Udvardy Enikő, Redl Pál, Márton Ildikó: Biszfoszfonát-kezelés során fellépő

állcsontnecrosis. Magyar Onkológia 52:81-87, 2008.

52. Szabó A, Szentandrássy N, Birinyi P, Horváth B, Szabó G, Bányász T, Márton I,

Magyar J, Nánási PP: Effects of ropivacaine on action potential configuration and

ion currents in isolated canine ventricular cardiomyocytes. Anesthesiology 108: 693-

702, 2008. IF: 5.124

53. Marincsák R, Tóth BI, Czifra G, Márton I, Redl P, Tar I, Tóth L, Kovács L, Bíró T:

Increased expression of TRPVI in squamous cell carcinoma of the human tongue.

Oral Diseases 15:328-335, 2009. IF: 1.922

54. Dr. Tar Ildikó, Dr. Márton Ildikó: Az orális lichen planus: bizonyosságok és

kétségek (irodalmi áttekintés)

Fogorv Szle 102:103-109, 2009.

55. Szarka K, Tar I, Fehér E, Kis A, D Tóth E, Boda R, Márton I, Gergely L:

Progressive increase of human paillomavirus carriage rates in potentially malignant

and malignant oral disorders with incresing malignant potential.

Oral Microbiol Immunol 24:314-318, 2009. IF: 2.336

56. Varga I, Sóczó G, Kardos G, Kemény-Beke A, Kelentey B, Márton I, Majoros L:

Difference in killing activity of caspofungin and paradoxical growt h between

Candida albicans and C. krusei clinical isolates in different media.

J Chemother 21:36-41, 2009. (2008.évi IF) IF: 1.166

57. Bágyi K, Haczku A, Márton I, Szabó J, Gáspár A, Andrási M, Varga I, Tóth J,

Klekner A: Role of pathogenic oral flora in postoperative pneumonia following brain

surgery. BMC Infectious Diseases, 9:104-, 2009. IF: 2.550

58. Hernádi K, Szalmás A, Mogyorósi R, Czompa L, Veress G, Csoma E, Márton I,

Kónya J: Prevalence and activity of Epstein-Barr virus and human cytomegalovirus

in symptomatic and asymptomatic apical periodontitis lesions. J Endod 36:1485-

1489, 2010. (2009.évi IF) IF:2.953

59. Szentandrássy N, Szabó A, Almássy J, Jóna I, Horváth B, Szabó G, Bányász T,

Márton I, Nánási P, Magyar J: Effects of articaine and ropivacaine on calcium

7

handling and contractility in canine ventricular myocardium. Eur. J Anaesthesiol

27:153-161, 2010. (2009.évi IF) IF:1.859

60. Dr. Martos Renáta, Dr. Márton Ildikó: A fogágybetegség és a krónikus obstruktív

tüdőbetegség (COPD) lehetséges összefüggései (Irodalmi áttekintés) Fogorv Szle

(közlésre benyújtva)

61. Tar I, Szarka K, Veres I, Cseh A, Varga I, Martos R, Kiss Cs, Márton IJ:

Coinciding Disorders in Oral Leukoplakia and Lichen Planus. J. Dent Res (beküldés

alatt)

62. Török J, Vitalyos G, Kovalecz G, Nemes J, Alberth M, Márton I: The role of

orthodontics int the complex treatment of dental traumas.

Dent Traumatol (beküldés alatt)

63. Radics T., Márton I.: Can chronic apical periodontitis lesions cause the same

systemic effects as marginalis inflammatory processes? (közlésre benyújtva)

In extenso közlemények kumulatív impakt faktora: 49.52

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ABSZTRAKTOK

A kandidátusi fokozat megszerzése előtt, lektorált folyóiratban megjelent, citálható

absztraktok:

IF

- A1.Márton IJ, Johnson S, Knowles BB: SV 40 Tag transgenic mice as a model for

Autoimmunity and Tumorigenicity.

8 th

International Congress of Immunology Budapest, 1992.

Springer Hungarica Budapest, p.421, 1992.

- A2.Márton IJ, Kiss C: Immunoregulatory and inflammatory changes in apical

periodontitis.

Int Endod J 23:62, 1990. - 4th

E.S.E. Congress, Amsterdam, 1989. IF:0,576

Az előadott abstract és pályázati anyaga elnyerte az E.S.E. „ Research Prize”-át

A kandidátusi fokozat megszerzését követően, lektorált folyóiratban megjelent,

citálható absztraktok:

- A3.Juhász A, Hegedűs C, Flóra-Nagy E, Márton I: Semi-quantitative three-

dimensional leakage study of three endodontic sealers.

Int Endod J 96:29, 1995.- 5th

E.S.E. Congress, Jerusálem, 1995 IF:0.473

- A4.Márton IJ, Johnson S, Kiss C, Knowles BB: Mice transgenic for an SV 40 tumor

antigen (Tag) hybrid gene as an animal model for tumorigenicity and autoimmunity.

Med Pediatr Oncol 25:325, 1995. - SIOP Meeting, Montevideo, 1995. IF:1.543

- A5. Kiss C, Nemes Z, Márton IJ, Vályi-Nagy I, Rot A: Expression of chemokine

family of inflammatory cytokines in Rosai-Dorfman-Type histiocytosis.

Med Pediatr Oncol 29:461, 1997.- SIOP Meeting, Istanbul, 1997. IF:1.693

- A6. Márton IJ, Rot A, Radics T, Vályi-Nagy, Kiss C: Expression of chemokine family

of inflammatory cytokines in chronic apical periodontitis.

Int Endod J 31:205, 1998.- 8th

E.S.E. Congress, Gothenburg, 1997. IF:0.718

- A7. Radics T, Tar I, Márton I: Types and prevalence of human periapical lesions,

significance of Histologicaal evaluation.

Int Endod J 33:163, 2000.- 9th E.S.E. Congress, Zagreb, 1999. IF:0.933

- A8. Tar I, Radics T, Márton IJ: Screening of chronic inflammatory dental disorders in

focal diseases.

9

Int Endod J 33:167, 2000.-10th

E.S.E. Congress, Zagreb, 1999. IF:0.933

- A9. Radics T, Tar I, Kiss C, Márton IJ.: Interleukin-6 and GM-CSF in apical

periodontitis: correlation between clinical and histological findings.

Int Endod J 35:117, 2002.-11th

E.S.E. Congress, Munnich, 2001. IF:0.974

Citálható absztraktok kumulatív impakt faktora: 7.843

In extenso közlemények impakt faktora: 49.52

Citálható absztraktok impakt faktora: 7.843

Kumulatív Impakt Faktor: 57.363

IF=impakt faktor (a megjelenés éve szerint)

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KÖNYVRÉSZLETEK

A kandidátusi fokozat megszerzését követően megjelent könyvrészletek:

1. Márton I: Fog-és szájbetegségek. In: Síró B. (Ed.): Gyakorlati Geriátria.

Springer Hungarica Kiadó Kft. 1999. pp. 212-216,

2. Márton I:. Fogászati betegségek és a vese. In: Kakuk Gy. (Ed.) Klinikai Nephrológia.

Medicina Könyvkiadó Rt. 2004. pp. 1084-1091,

3. Márton I: A szájüreg betegségei. In: Oláh É., (Ed.) Gyermekgyógyászati protokollok.

Medicina Könyvkiadó Rt. 2004. pp. 1469-1488, (2007. II. kiadás)

4. Márton I: A leggyakoribb fogászati betegségek. In: Ádány R., (Ed) Népegészségügyi

Medicina (szerkesztés alatt)

11

Dr. Márton Ildikó Judit referált folyóiratokban közölt cikkeire és citálható

absztraktjaira történt szakirodalmi hivatkozások - 2010. 09. 27.-i állapot,

önidézettséggel együtt. Citált közlemény aláhúzva, a rá történt hivatkozások száma

jobbra zárva (zárójelben önidézettség nélkül) + önidézettség, alatta a citáló

közlemény(ek) specifikációi

a Web of Science és Scopus adatbázisok, ill. saját gyűjtés alapján

Ad Marton I, Harmati S, Kiss C: Immunologische Veranderungen bei

patienten mit periapikalem Granulom. Z Stomatol 84:93-99, 1987. (1)

Radics T: Gondolatok az apicalis periodontitis korszerű kezeléséről.

Magyar Fogorvos 11:254-255, 2002.

Ad Marton I, Kiss C, Balla G, Szabó T, Karmazsin L: Acute phase proteins in

patients with chronic periapical granuloma before and after surgical

treatment. Oral Microbiol Immunol 3:95-96, 1988. (6)+2

Lerner UH: Regulation of bone metabolism by the kallikrein-kinin system,

the coagulation cascade, and the acute-phase reactants. Oral Surg Oral Med

Oral Pathol 78:481-493, 1994.

Márton IJ, Kiss C: Protective and destructive reaction in apical

periodontitis. Oral Microbiol Immunol 15:139-150, 2000.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Radics T: Gondolatok az apicalis periodontitis korszerű kezeléséről.

Magyar Fogorvos 11:254-255, 2002.

Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the

involved teeth. Oral Microbiol Immunol 18:9-13, 2003.

Caplan DJ: Epidemiologic issues in studies of association between apical

periodontitis and systemic health. Endod Topics 8:15-35, 2004.

Caplan DJ, Chasen JB, Krall EA, Cai J, Kang S, Garcia RI, Offenbacher S,

Beck JD: Lesions of endodontic origin and risk of coronary heart disease. J

Dent Res 85:996-1000, 2006.

Caplan, D.J., Pankow, J.S., Cai, J., Offenbacher, S., Beck, J.D.: The

relationship between self-reported history of endodontic therapy and

coronary heart disease in the Atherosclerosis Risk in Communities Study. J

Am Denl Assocon 140:1004-1012, 2009.

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Ad Márton IJ, Rédei I, Kelentey B, Lázár S, Ölveti É: Granuloma apicalés

fogak gyökércsatorna bennékének mikrobiológiai vizsgálata. Fogorv Szle

81:245-248, 1988. (3)+1

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Radics T: Gondolatok az apicalis periodontitis korszerű kezeléséről.

Magyar Fogorvos 11:254-255, 2002.

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Nemes J, Duhaj Sz, Nyárasdy I: A fogbélbetegségek és a fogbél

következményes betegségeinek terápiájában(gyökérkezelés) bekövetkezett

változások 100 éve a Fogorvosi Szemle közleményeinek tükrében (1908-

2008). Fogorv Szle 101:127-136, 2008.

Ad Márton I, Mórocz I: Periapikális granulómák szövettani vizsgálata. Fogorv

Szle 82:365-368, 1989. ( )+1

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Ad Marton I, Nemes Z, Harmati S: Quantitative significance of IgE producing

plasma cells and tissue distribution of mast cells in apical periodontitis. Oral

Microbiol Immunol 5:46-48, 1990. (7)+3

Kiss C: Regulation of gene expression in human leukemic cell lines: effect

of c-kit ligand. Alpe Adria J Med 49:42-44, 1994.

Okiji T: Class II MHC Molecule-expressing Cells of the Dental Pulp.

(Thesis) Göteborg University Press, Göteborg, Sweden, 1996.

Márton IJ, Dezső B, Radics T, Kiss C: Distribution of interleukin-2 receptor

-chain and cells expressing major histocompatibility complex class II

antigen in chronic human periapical lesions. Oral Microbiol Immunol

13:259-262, 1998.

Márton IJ, Kiss C: Protective and destructive reaction in apical

periodontitis. Oral Microbiol Immunol 15:139-150, 2000.

Márton IJ, Rot A, Schwarzinger E, Szakáll Sz, Radics T, Vályi-Nagy I, Kiss

C: Differential in situ distribution of IL-8, MCP-1 and Rantes factor in

human chronic periapical granuloma. Oral Microbiol Immunol 15:63-65,

2000.

13

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Rodini CD, Batista AC, Lara VS: Comparative immunohistochemical study

of the prewcence of mast cells in apical granulomas and periapical cysts:

Possible role of mast cells int he course of human periapical lesions. Oral

Surg Oral Med Oral Pathol Oral Radiol Endod 97:59-63, 2004.

Ledesma-Montes C, Garces-Ortiz M, Rosales-Garcia G, Hernandez-

Guerrero JC Importance of mast cells in human periapical inflammatory

lesions. Journal of Endodontics 30:855-859, 2004 .

Čolić, M., Gazivoda, D., Vučević, D., Vasilijić, S., Rudolf, R., Lukić, A.:

Proinflammatory and immunoregulatory mechanisms in periapical lesions.

Molecul Immunol 47:101-113, 2009.

Dražić, R., Sopta, J., Minić, A.J.: Mast cells in periapical lesions: Potential

role in their pathogenesis. J Oral Pathol Med 39:257-262, 2010.

Ad Marton I, Kiss C, Szabó T: Akut-fázis fehérjék szerepe a kronikus

periapikalis granuloma patogenezisében. Fogorvosi Szle 83: 235-239, 1990.

(1)

Buttke BM, Shipper G, Delano EO, Trope M: C-reactive protein and serum

amyloid A in a canine model of chronic apical periodontitis. J Endod 31:

728-732, 2005.

Ad Marton IJ, Kiss C: Influence of surgical treatment of periapical lesions on

serum and blood levels of inflammatory mediators. Int Endod J 25:229-233,

1992. (9)+5

Moseley R, Waddington R, Evans P, Halliwell B, Embery G: The chemical

modification of glycosaminoglycan structure by oxygen-derived species in

vitro. BBA-Gen Subjects 1244:245-252, 1995.

Takahashi K: Microbiological, pathological, inflammatory, immunological

and molecular biological aspects of periradicular disease. Int Endod J

31:311-325, 1998.

Márton IJ, Dezső B, Radics T, Kiss C: Distribution of interleukin-2 receptor

-chain and cells expressing major histocompatibility complex class II

antigen in chronic human periapical lesions. Oral Microbiol Immunol

13:259-262, 1998.

Márton IJ, Kiss C: Protective and destructive reaction in apical

periodontitis. Oral Microbiol Immunol 15:139-150, 2000.

14

Márton IJ, Rot A, Schwarzinger E, Szakáll Sz, Radics T, Vályi-Nagy I, Kiss

C: Differential in situ distribution of IL-8, MCP-1 and Rantes factor in

human chronic periapical granuloma. Oral Microbiol Immunol 15:63-65,

2000.

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Radics T: Gondolatok az apicalis periodontitis korszerű kezeléséről.

Magyar Fogorvos 11:254-255, 2002.

Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the

involved teeth. Oral Microbiol Immunol 18:9-13, 2003.

Caplan DJ: Epidemiologic issues in studies of association between apical

periodontitis and systemic health. Endod Topics 8: 15-35, 2004.

Buttke BM, Shipper G, Delano EO, Trope M: C-reactive protein and serum

amyloid A in a canine model of chronic apical periodontitis. J Endod 31:

728-732, 2005.

Wu MK, Dummer PMH, Wesselink PR: Consequences of and strategies to

deal with residual post-treatment root canal infection. Int Endod J 39: 343-

356, 2006.

Caplan DJ, Chasen JB, Krall EA, Cai J, Kang S, Garcia RI, Offenbacher S,

Beck JD: Lesions of endodontic origin and risk of coronary heart disease. J

Dent Res 85: 996-1000, 2006.

Caplan DJ, Pankow JS, Cai J, Offenbacher S, Beck JD: The relationship

between self-reported history of endodontic therapy and coronary heart

disease in the Atherosclerosis Risk in Communities Study.J Am Dent Assoc

140:1004-1012, 2009.

Ad Marton IJ, Kiss C: Characterization of inflammatory cell infiltrate in dental

periapical lesions. Int Endod J 26:131-136, 1993. (43)+4

Okiji T: Class II MHC Molecule-expressing Cells of the Dental Pulp.

(Thesis) Göteborg University Press, Göteborg, Sweden, 1996.

Kawashima N, Okiji T, Kosaka T, Suda H: Kinetics of macrophages and

lymphoid cells during the development of experimentally induced periapical

lesions in rat molars: A quantitative immunohistochemical study. J Endod

22:311-316, 1996.

15

Nair PNR: Apical periodontitis: A dynamic encounter between root

canalinfection and host response. Periodontology 2000 13:121-148, 1997.

Delzangles B, BoyLefevre ML, Forest N: Glycoproteins expression in

apical pathologic tissues: Clinicalincidences. J Endod 23:565-568, 1997.

Llamas R, Segura JJ, JimenezRubio A, JimenezPlanas A: In vitro effect of

parachlorophenol and camphorated parachlorophenol on macrophages. J

Endod 23:728-730, 1997.

Segura JJ, Jimenez-Rubio A, Guerrero JM, Calvo JR, Feito JJ: Effect in

vitro of Tifell (formocresol-eugenol) on macrophage adhesion. Int Endod J

31:112-116, 1998.

Alavi AM, Gulabivala K, Speight PM: Quantitative analysis of lymphocytes

and their subsets in periapical lesions. Int Endod J 31:233-240,1998.

Takahashi K: Microbiological, pathological, inflammatory, immunological

and molecular biological aspects of periradicular disease. Int Endod J

31:311-325, 1998.

Stashenko P, Teles R, Dsouza R: Periapical inflammatory responses and

their modulation. Critical Rev Oral Biol Med 9:498-521, 1998.

Márton IJ, Dezső B, Radics T, Kiss C: Distribution of interleukin-2 receptor

-chain and cells expressing major histocompatibility complex class II

antigen in chronic human periapical lesions. Oral Microbiol Immunol

13:259-262, 1998.

Sol MA, Tkaczuk J, Voigt JJ, Durand M, Sixou M, Maurette A, Thomsen

M: Characterization of lymphocyte subpopulations in periapical lesions by

flow cytometry. Oral Microbiol Immunol 13:253-258, 1998.

Takahashi K, MacDonald DG, Murayama Y, Kinane DF: Cell synthesis,

proliferation and apoptosis in human dental periapical lesions analysed by

in situ hybridisation and immunohistochemistry. Oral Dis 5:313-320, 1999.

Segura JJ, Jimenez-Rubio A, Guerrero JM, Calvo JR: Comparative effects

of two endodontic irrigants, chlorhexidine digluconate and sodium

hypochlorite, on macrophage adhesion to plastic surfaces. J Endod 25:243-

246, 1999.

Suzuki N, Okiji T, Suda H: Enhanced expression of activation-associated

molecules on macrophages of heterogeneous populations in expanding

periapical lesions in rat molars. Arch Oral Biol 44:67-79, 1999.

Moreira PR, Santos DFM, Martins RD, Gomez RS: CD57(+) cells in

radicular cyst. Int Endod J 33:99-102, 2000.

Fernando K, Gulabivala K, Barrett AW: The preparation of periapical

lesions for flow cytometry. Int Endod J 33:103-112, 2000.

16

Tasman F, Er N, Atac A, Dagdeviren A, Kendir B: CD45/isotypes

expression in the immune cells of human periapical lesions. J Endod

26:166-168, 2000.

Márton IJ, Kiss C: Protective and destructive reaction in apical

periodontitis. Oral Microbiol Immunol 15:139-150, 2000.

Kaneko T, Okiji T, Kan L, Takagi M, Suda H: Ultrastructural analysis of

MHC class II molecule-expressing cells in experimentally induced

periapical lesions in the rat. J Endod 27:337-342, 2001.

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Nair PNR: Pathobiology of the Periapex. In: Cohen S, Burns RC (Eds):

Pathways of the pulp. Mosby, pp. 457-500, 2002.

Sartori, S., Silvestri, M., Cattaneo, V: Endoperiodontal lesion: A case

report. J Clin Periodont 29:781-783, 2002.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Radics T: Gondolatok az apicalis periodontitis korszerű kezeléséről.

Magyar Fogorvos 11:254-255, 2002.

Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the

involved teeth. Oral Microbiol Immunol 18:9-13, 2003.

Liapatas S, Nakou M, Rontogianni D Inflammatory infiltrate of chronic

periradicular lesions: an immunohistochemical study. Int Endod J 36:464-

471, 2003.

Slots J, Sabeti M, Simon JH: herpesviruses in periapical pathosis: An

etiopathogenic relationship Oral Surg Oral Med Oral Pathol Oral Radiol

Endod 96:327-331, 2003.

Rodini CD, Batista AC, Lara VS: Comparative immunohistochemical study

of the prewcence of mast cells in apical granulomas and periapical cysts:

Possible role of mast cells int he course of human periapical lesions. Oral

Surg Oral Med Oral Pathol Oral Radiol Endod 97:59-63, 2004.

Nair PNR: Pathogenesis of apical periodontitis and the causes of endodontic

failures. Critical Reviews in Oral Biology & Medicine 15:348-381, 2004.

Ricucci D, Bergenholtz G: Histologic features of apical periodontitis in

human biopsies. Endod Topics 8:68-87, 2004.

17

Leonardi R, Caltabiano R, Loreto C: Collagenase-3 (MMP-13) is expressed

in periapical lesions: an immunohistochemical study. Int Endod J 38:297-

301, 2005.

Lukic A, Vasilijic S, Majstorovic I, Vucevic D, Mojsilovic S, Gazivoda D,

Danilovic V, Petrovic R, Colic M: Characterization of antigen-presenting

cells in human apical periodontitis lesions by flow cytometry and

immunocytochemistry. Int Endod J 39: 626-636, 2006.

Lukic A, Vojvodic D, Majstorovic I, Colic M: Production of interleukin-8

in vitro by mononuclear cells isolated from human periapical lesions. Oral

Microbiol Immunol 21: 296-300, 2006.

Jankowska-Antczak, E., Włodarski, K., Wojtowicz, A.:

okołowierzchołkowych po przeszczepieniach narzadowych].

Implantoprotetyka 7:2-6, 2006.

Caviedes-Bucheli J, Azuero-Holguin MM, Moreno GC, Gonzalez IL, Mateu

E, Salazar JF, Munoz HR: Vasoactive intestinal peptide receptor expression

in chronic periapical lesions. Internatl Endod J 40: 521-525, 2007.

Wang L, Peng B: Correlation between platelet-derived growth factor B

chain and bone resorption in rat periapical lesions. J Endod 33: 709-711,

2007.

Andric M, Milasin J, Jovanovic T, Todorovic L.: Human cytomegalovirus is

present in odontogenic cysts. Oral Microbiol Immunol 5:347-351, 2007.

Cogulu D, Oncag O, Kutukculer N, Uzel A, Eronat C: The Correlation

between Serum Immunoglobulin A and Immunoglobulin G Levels and the

Presence of Treponema denticola in Human Periapical Lesions. J Endod 33:

1413-1416, 2007.

Saboia-Dantas CJ, de Toledo LFC, Siqueira JF, Sampaio-Filho HR,

Carvalho JJ, Pereira MJS: Natural killer cells and alterations in collagen

density: signs of periradicular herpesvirus infection? Clin Oral Invest

12:129-135, 2008.

Bolan M, Lima DD, Figueiredo CP, Di Giunta G, Rocha MJD:

Immunohistochemical Study of Presence of T Cells, B Cells, and

Macrophages in Periradicular Lesions of Primary Teeth. J Clin Pediatr Dent

32:287-293, 2008.

Xiong HF, Wei LL, Peng B: Immunohistochemical Localization of IL-17 in

Induced Rat Periapical Lesions. J Endod 35:216-220, 2009.

Garcia CC, Diago MP, Mira BG, Sebastian JVB, Sempere FV: Expression

of cytokeratins in epithelialized periapical lesions. Oral Surg Oral Med Oral

Pathol Oral Radiol Endodontol 107:E43-E46, 2009.

18

Gazivoda D, Dzopalic T, Bozic B, Tatomirovic Z, Brkic Z, Colic M:

Production of proinflammatory and immunoregulatory cytokines by

inflammatory cells from periapical lesions in culture. J Oral Pathol Med

38:605-611, 2009.

Colic M, Gazivoda D, Vucevic D, Vasilijic S, Rudolf R, Lukic A:

Proinflammatory and immunoregulatory mechanisms in periapical lesions.

Mol Immunol 47:101-113, 2009.

Zhang, C., Yang, L., Peng, B: Critical role of NFATc1 in periapical

lesions. Int Endod J 43:109-114, 2010.

Dražić, R., Sopta, J., Minić, A.J.: Mast cells in periapical lesions: Potential

role in their pathogenesis. Journal of Oral Pathology and Medicine 39:257-

262, 2010.

Carrillo, C., Peñarrocha, M., Peñarrocha, M., Vera, F., Peñarrocha, D.:

Immunohistochemical study of Langerhans cells in periapical lesions;

correlation with inflammatory cell infiltration and epithelial cell

proliferation. Medicina Oral, Patologia Oral y Cirugia Bucal 15:e335-e339,

2010.

Ad Marton IJ, Balla G, Hegedűs C, Redl P, Szilágyi Z, Karmazsin L, Kiss C:

The role of reactive oxygen intermediates in the pathogenesis of chronic

apical periodontitis. Oral Microbiol Immunol 8: 254-257, 1993. (20)+2

Moseley R, Waddington RJ, Embery G: Degradation of

glycosaminoglycans by reactive oxygen species-derived from stimulated

polymorphonuclear leukocytes. Biochem Biophys Acta – Molec Basis

Disease 1362:221-231, 1997.

Moseley R, Waddington RJ, Embery G, Rees SG: The modification of

alveolar bone proteoglycans by reactive oxygen species in vitro Connective.

Tissue Res 37:13-28, 1998.

Battino M, Bullon P, Wilson M, Newman H: Oxidative injury and

inflammatory periodontal diseases: The challenge of antioxidants to free

radicals and reactive oxygen species. Crit Rev Oral Biol Med 10:458-476,

1999.

Márton IJ, Kiss C: Protective and destructive reaction in apical

periodontitis. Oral Microbiol Immunol 15:139-150, 2000.

Waddington RJ, Moseley R, Embery G: Reactive oxygen species: A

potential role in the pathogenesis of periodontal diseases. Oral Dis 6:138-

151, 2000.

19

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Yeung SY, Lan WH, Huang CS, Lin CP, Chan CP, Chang MC, Jeng JH:

Scavenging potential of three cresol isomers against H2O2, hypochlorite,

superoxide and hydroxyl radicals. Food Chem Toxicol 40:1403-1413, 2002.

Ritchie CS, Kinane DF: Nutrition, inflammation, and periodontal disease.

Nutrition 19: 475-476, 2003.

Kayaoglu G, Orstavik D: Virulence factors of Enterococcus faecalis:

Relationship to endodontic disease. Critical Reviews nn Oral Biology &

Medicine 15: 308-320, 2004.

Akalin FA, Toklu E, Renda N: Analysis of superoxide dismutase activity

levels in gingiva and gingival crevicular fluid in patients with chronic

periodontitis and periodontally healthy controls. J Clin Periodontol 32: 238-

243, 2005.

Tsai CC, Chen HS, Chen SL, Ho YP, Ho KY, Wu YM, Hung CC: Lipid

peroxidation: a possible role in the induction and progression of chronic

periodontitis. J Periodont Res 40: 378-384, 2005.

Canakci CF, Cicek Y, Canakci V: Reactive oxygen species and human

inflammatory periodontal diseases. Biochem-Moscow 70: 619-628, 2005.

Celec P, Hodosy J, Celecova V, Vodrazka J, Cervenka T, Halcak L, Bozek

P, Kopani M, Kudela M: Salivary thiobarbituric acid reacting substances

and malondialdehyde - Their relationship to reported smoking and to

parodontal status described by the papillary bleeding index. Disease

Markers 21:133-137, 2005.

Akalin FA, Baltacioglu E, Alver A, Karabulut E, Lipid peroxidation levels

and total oxidant status in serum, saliva and gingival crevicular fluid in

patients with chronic periodontitis. J Clin periodontol 34:558-565, 2007.

Yeung SY, Huang CS, Chan CP, Lin CP, Lin HN, Lee PH, Jia HW, Huang

SK, Jeng JH Chang MC: Antioxidant and pro-oxidant properties of

chlorhexidine and its interaction with calcium hydroxide solutions

Int Endod J 11:837-844, 2007.

Akalin FA, Isiksal E, Baltacioglu E, Renda N, Karabulut E: Superoxide

dismutase activity in gingiva in type-2 diabetes mellitus patients with

chronic periodontitis. Arch Oral Biol 53:44-52, 2008.

Moynihan P: Update on nutrition and periodontal disease. Quintessence Int

39:326-330, 2008.

20

Khalili J, Biloklytska HF: Salivary malondialdehyde levels in clinically

healthy and periodontal diseased individuals. Oral Diseas 14: 754-760,

2008.

Su HX, Gornitsky M, Velly AM, Yu HL, Benarroch M, Schipper HM:

Salivary DNA, lipid, and protein oxidation in nonsmokers with periodontal

disease. Free Radical Biology and Medicine 46:914-921, 2009.

Wei D, Zhang XL, Wang YZ, Yang CX, Chen G: Lipid peroxidation levels,

total oxidant status and superoxide dismutase in serum, saliva and gingival

crevicular fluid in chronic periodontitis patients before and after periodontal

therapy. Aust Dent J 55: 70-78, 2010.

Xiang XM, Liu KZ, Man A, Ghiabi E, Cholakis A, Scott DA: Periodontitis-

specific molecular signatures in gingival crevicular fluid .J Periodont 45:

345-352, 2010.

Ad Marton IJ, Rot A, Radics T, Vályi-Nagy I, Kiss C: Expression of

chemokine family of inflammatory cytokines in chronic apical periodontitis.

8 Bienn C Eur Soc E 13, 1997. (1)+1

Huang GTJ, Potente AP, Kim JW, Chugal N, Zhang XL: Increased

interleukin-8 expression in inflamed human dental pulps. Oral Surg Oral

Med Oral Pathol 88:214-220, 1999.

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Ad Marton IJ, Dezső B, Radics T, Kiss C: Distribution of interleukin-2

receptor chain and class II antigen expressing cells in chronic human

periapical lesions. Oral Microbiol Immunol 13:259-262, 1998. (4)+4

Márton IJ, Kiss C: Protective and destructive reaction in apical

periodontitis. Oral Microbiol Immunol 15:139-150, 2000.

Márton IJ, Rot A, Schwarzinger E, Szakáll Sz, Radics T, Vályi-Nagy I, Kiss

C: Differential in situ distribution of IL-8, MCP-1 and Rantes factor in

human chronic periapical granuloma. Oral Microbiol Immunol 15:63-65,

2000.

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

21

Hogan LH, Wang M, Suresh M, Co DO, Weinstock JV, Sandor M: CD4(+)

TCR repertoire heterogeneity in Schistosoma mansoni-induced granulomas.

J Immunol 169: 6386-6393, 2002.

Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the

involved teeth. Oral Microbiol Immunol 18:9-13, 2003.

Han DC, Huang GTJ, Lin LM, Warner NA, Gim JS, Jewet A: Expression of

MHC Class II. CD70, CD80, CD86 and pro-inflammatory cytokines in

differentialy regulated in oral epithelial cells following bacterial challenge.

Oral Microbiol Immunol 18:350-358, 2003.

Tadokoro O, Radunovic V, Inoue K: Epithelial cell rests of malassez and

OX6-immunopositive cells in the periodontal ligament of rat molars: A light

and transmission electron microscope study. Anat Record-Advances

Integrative Aanat Evol Bbiol 291: 242-253, 2008.

Ad Márton I, Bágyi K, Radics T, Kiss C: Az apicalis periodontitis kialakulása

és szervezetre gyakorolt hatása. Fogorv Szle 91:269-273, 1998. (2)+1

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Nemes J, Duhaj Sz, Nyárasdy I: A fogbélbetegségek és a fogbél

következményes betegségeinek terápiájában (gyökérkezelés) bekövetkezett

változások 100 éve a Fogorvosi Szemle közleményeinek tükrében (1908-

2008). Fogorv Szle 101:127-136, 2008.

Ad Mikala G, Berencsi G, Kiss C, Márton I, Domján G, Vályi-Nagy I: Human

herpesvirus 8 in hematologic diseases. Pathol Oncol Res 5:73-79; 1999.(16)

Cummings TJ, Gong JZ, Friedman AH, McLendon RE: Castleman's disease

confined to the leptomeninges. Ann Clin Lab Sci 30:278-282, 2000.

Burmeister T, Thiel E: Molecular genetics in acute and chronic leukemias. J

Cancer Res Clin Oncol 127:80-90, 2001.

Saif, M.W.: Castleman disease in an HIV-infected patient with Kaposi

sarcoma. AIDS Reader 11:572-574, 2001.

22

Ding I, Volz S, Schmitt HJ: Human herpes 8 virus. Padiatrische Praxis

61:249-261, 2002.

Sola P, Bedin R, Casoni F, Barozzi P, Mandrioli J, Merelli E: New insights

into the viral theory of amyotrophic lateral sclerosis: study on the possible

role of kaposi’s sarcoma-associated virus/human herpesvirus 8. Eur Neurol

47:108-112, 2002.

de Sanjose S, Goedert JJ, Marshall V, Bellas C, Benavente Y, Bosch R,

Domingo A, Fernandez A, de Sevilla AF, Servitje O, Whitby D: Risk of

malignant lymphoma associated with human herpesvirus-8: a case-control

study in Spain. Br J Cancer 90:2145-2148, 2004.

Deftereos S, Farmakis D, Papadogianni A, Besleme B, Diamanti-

Kandarakis E, Polymeropoylos E, Georgonikou D, Aessopos A:

Waldenstrom's macroglobulinemia developing in a patient with multiple

sclerosis: coincidence or association? Multiple Sclerosis 10:598-600, 2004.

Wang J, Bu DF, Li T, Zheng R, Zhang BX, Chen XX, Zhu XJ:

Autoantibody production from a thymoma and a follicular dendritic cell

sarcoma associated with paraneoplastic pemphigus. Br J Dermatol 153:558-

564, 2005.

Jaffar, S.A., Pihan, G., Dezube, B.J., Pantanowitz, L: Differentiating HIV-

associated lymphomas that exhibit plasmacellular differentiation. HIV and

AIDS Review 4:43-49, 2005.

Henke-Gendo C, Mengel M, Hoeper MM, Alkharsah K, Schulz TF:

Absence of Kaposi's sarcoma-associated herpesvirus in patients with

pulmonary arterial hypertension. Am J Respirat Critical Care Medicin

172:1581-1585, 2005.

Pantanowitz, L., Wu, Z., Dezube, B.J., Pihan, G: Extracavitary primary

effusion lymphoma of the anorectum. Clin Lymph Myel 6:149-152, 2005.

Perdaens C, De Raeve H, Goossens A, Sennesael J: POEMS syndrome

characterized by glomeruloid angioma, osteosclerosis and multicentric

Castleman disease. J Eur Aacad Dermatol Venereol 20: 480-481, 2006.

Szegedi, I., Kiss, C., Karászi, É., Vámosi, G., Szöllosi, J., Kovács, P.,

Benko, I: Differential regulation of umbilical cord blood and leukemic B

cells by interferon-alpha (IFN-α): Observations in cultured cells. Pathol

Oncol Res 12:159-163, 2006.

Csire, M., Mikala, G., Peto, M., Jánosi, J., Juhász, A., Tordai, A., Jákó, J.,

(...), Vályi-Nagy, I: Detection of four lymphotropic herpesviruses in

Hungarian Patients with multiple myeloma and lymphoma. FEMS Immunol

Med Microbiol 49:62-67, 2007.

Bacha, M.M., Goucha, R., Zouaghi, K., Jebali, H., Fazaa, B., Hedri, H., El

Younsi, F., (...), Kheder, A: Myeloma, Kaposi's sarcoma and HHV8

infection in hemodialysed patient | [Myelome multiple, maladie de Kaposi

23

et infection par le HHV8 chez un hemodialyse chronique]. Tunis Med

85:237-239, 2007.

Pantanowitz, L., German, P., Carbone, A., Dezube, B.J: Differentiating

HIV-associated non-Hodgkin's lymphomas with similar plasmacellular

differentiation. J HIV Ther 14:24-33, 2009.

Ad Márton I, Radics T, Szakáll Sz, Kiss C: A sejtes összetétel, az aktivált

állapotú sejtek vizsgálata granuloma apicaleban. Fogorv Szle 92:379-385,

1999. ( )+1

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Ad Márton I, Johnson SE, Damjanov I, Currie KS, Sundberg JP, Knowles B:

Expression and immune recognition of SV40 Tag in transgenic mice that

develop SV40 Tag-induced metastaic osteosarcomas.

Transgenic Res 9:115-125, 2000. (10)+1

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Joliat MJ, Umeda S, Lyons BL, Lynes MA, Shultz LD: Establishment and

characterization of a new osteogenic cell line (MOS-J) from a spontaneous

C57BL/6J mouse osteosarcoma. In Vivo 16:223-228, 2002.

Staveley-O'Carroll K, Schell TD, Jimenez M, Mylin LM, Tevethia MJ,

Schoenberger SP, Tevethia SS: In vivo ligation of CD40 enhances priming

against the endogenous tumor antigen and promotes CD8+ T cell effector

function in SV40 T antigen transgenic mice. J Immunology 171:697-707,

2003.

Stakhar G, Ben-Eliyahu S: Potential prophylactis measures againts

postoperative immunosuppression: Could they reduce recurrence rates in

oncological patients? Ann Surg Oncol 10: 972-992, 2003.

Schell TD: In Vivo Expansion of the Residual Tumor Antigen-Specific

CD8+ T Lymphocytes That Survive Negative Selection in Simian Virus 40

T-Antigen-Transgenic Mice. J Virology 78:1751-1762, 2004.

Hansen K, Khanna C: Spontaneous and genetically engineered animal

models: use in preclinical cancer drug development. Europ J of Cancer

40:858-880, 2004.

24

Sun Q, Feng J, Wei XL, Zhang R, Dong SZ, Shen Q, Dong J, Li HD, Hu

YH: Generation and characterization of a transgenic mouse model for

pancreatic cancer World Journal of Gastroenterology 12: 2785-2788, 2006.

Otahal P, Schell TD, Hutchinson SC, Knowles BB, Tevethia SS: Early

immunization induces persistent tumor-infiltrating CD8+ T cells against an

immunodominant epitope and promotes lifelong control of pancreatic tumor

progression in SV40 tumor antigen transgenic mice. J Immunology

177:3089-3099, 2006.

Shen Q, Sun Q, Wei X, Dong J, Zhang R, Wu P, Jin Y, Feng, J, Li, H, Hu

Y.: Generation and characterization of islet cell tumor in pTet-on/pTRE-

SV40Tag double-transgenic mice model. J Bioscience and Bioengineering

104:14-21, 2007.

Otahal P, Knowles BB, Tevethia SS, Schell TD: Anti-CD40 conditioning

enhances the TCD8 response to a highly tolerogenic epitope and subsequent

immunotherapy of simian virus 40 T antigen-induced pancreatic tumors. J

Immunology 179:6686-6695, 2007.

Sun Q , Wei X, Feng J, Zhang R, Shen Q, Dong J, Jin Y, Dong S, Li H, Hu

Y.:

Involvement of insulin-like growth factor-insulin receptor signal

pathway in the transgenic mouse model of medulloblastoma. Cancer

Science 99:234-240, 2008.

Ad Marton IJ, Rot A, Schwartzinger E, Szakáll S, Radics T, Vályi-Nagy I,

Kiss C: Differential in situ distribution of interleukin-8, macrophage

chemoattractant protein-1 and Rantes in human chronic periapical

granuloma. Oral Microbiol Immunol 15:63-65, 2000. (14)+3

Márton IJ, Kiss C: Protective and destructive reaction in apical

periodontitis. Oral Microbiol Immunol 15:139-150, 2000.

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Mizgerd JP: Molecular mechanisms of neutrophil recruitment elicited by

bacteria in the lungs. Semin Immunol 14:123-132, 2002.

Haroune N, Combourieu B, Besse P, Sancelme M, Reemtsma T, Kloepfer

A, Diab A, Knapp JS, Baumberg S, Delort AM: Benzothiazole degradation

by Rhodococcus pyridinovorans strain PA: Evidence of a catechol 1,2-

dioxygenase activity. Appl Environ Microbiol 68: 6114-6120, 2002.

25

Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the

involved teeth. Oral Microbiol Immunol 18:9-13, 2003.

Komoda T, Yoshida K, Abe N, Sugiyama Y, Imachi M, Hirota H, Koshino

H, Hirota A: Tetrapetalone A, a novel lipoxigense inhibitor from

Streptomyces sp.Biosci Biotech Biochem 68:104-111, 2004.

Silva TA, Garlet GP, Lara VS, Martins W, Silva JS, Cunha FQ: Differential

expression of chemokines and chemokine receptors in inflammatory

periapical diseases. Oral Microbiol Immunol 20: 310-316, 2005.

Lukic A, Vojvodic D, Majstorovic I, Colic M: Production of interleukin-8

in vitro by mononuclear cells isolated from human periapical lesions. Oral

Microbiol Immunol 21: 296-300, 2006.

Fukushi E: Advanced NMR approaches for a detailed structure analysis of

natural products. Bioscience Biotechnology and Biochemistry 70: 1803-

1812, 2006.

Silva, T.A., Garlet, G.P., Fukada, S.Y., Silva, J.S., Cunha, F.Q: Chemokines

in oral inflammatory diseases: Apical periodontitis and periodontal disease.

J Dent Res 86:306-319, 2007.

Adachi, T., Nakanishi, T., Yumoto, H., Hirao, K., Takahashi, K., Mukai, K.,

Nakae, H., Matsuo, T: Caries-related bacteria and cytokines induce

CXCL10 in dental pulp. J Dent Res 86:1217-1222, 2007.

Takeichi O, Hama S, Iwata K, Ito K: Confocal immunolocalization of VE-

cadherin- and CXC chemokine-expressing endothelial cells in periapical

granulomas. Internatl Endod J 41: 401-407, 2008.

Min KS, Kim HI, Chang HS, Kim HR, Pae HO, Chung HT, Hong SH, Shin

HI, Hong CU , Lee SK, Kim EC: Involvement of mitogen-activated protein

kinases and nuclear factor-kappa B activation in nitric oxide-induced

interleukin-8 expression in human pulp cells. Oral Surg Oral Med Oral

Pathol Oral Radiol Endod 105:654-660, 2008.

Gazivoda D, Dzopalic T, Bozic B, Tatomirovic Z, Brkic Z, Colic M:

Production of proinflammatory and immunoregulatory cytokines by

inflammatory cells from periapical lesions in culture. J Oral Pathol Med 38:

605-611, 2009.

Garlet TP, Fukada SY, Saconato IF, Avila-Campos MJ, Aparecida da Silva

T, Garlet GP, de Queiroz Cunha F: CCR2 Deficiency Results in Increased

Osteolysis in Experimental Periapical Lesions in Mice. J Endod 36:244-250,

2010.

Fukushima A, Kajiya H, Izumi T, Shigeyama C, Okabe K, Anan H: Pro-

inflammatory Cytokines Induce Suppressor of Cytokine Signaling-3 in

Human Periodontal Ligament Cells. J Endod 36: 1004-1008, 2010.

26

Ad Marton IJ, Kiss C: Protective and destructive immune reactions in apical

periodontitis. Oral Microbiol Immunol 15:139-150; 2000. (58)+2

Rodini CD, Lara VS: Study of the expression of CD68(+) macrophages and

CD8(+) T cells in human granulomas and periapical cysts. Oral Surg Oral

Med Oral Pathol Oral Radiol Endod 92:221-227, 2001.

De Oliveira Rodini, C., Lara, V.S: Study of the expression of CD68+

macrophages and CD8+ T cells in human granulomas and periapical cyst.

Oral Surg, Oral Med, Oral Pathol, Oral Radiol Endod 92:221-227, 2001.

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Tar I, Martos R: A fogágybetegségek és az általános szervi megbetegedések

összefüggése. Fogorv Szle 95:73-77, 2002.

Kabashima H, Nagata K, Maeda K, Iijima T: Involvement of substance P,

mast cells, TNF-alpha and ICAM-1 in the infiltration of inflammatory cells

in human periapical granulomas. J Oral Pathol Med 31:175-158, 2002.

Nickolaychuk B, McNicol A, Gilchrist J, Birek C: Evidence for a role of

mitogen-activated protein kinases in proliferating odontogenic epithelia of

inflammatory and developmental cysts. Oral Surg Oral Med Oral Pathol

Oral Radiol Endod 93:720-729, 2002.

Radics T: Gondolatok az apicalis periodontitis korszerű kezeléséről.

Magyar Fogorvos 11:254-255, 2002.

Puliti M, von Hunolstein C, Bistoni F, Castronari R, Orefici G, Tissi L:

Role of macrophages in experimental group B streptococcal arthritis. Cell

Microbiol 4:691-699, 2002.

Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the

involved teeth. Oral Microbiol Immunol 18:9-13, 2003.

Sabeti M, Valles Y, Nowzari H, Simon JH, Kermani-Arab V, Slots J:

Cytomegalovirus and Epstein-Barr virus DNA transcription in endodontic

symptomatic lesions. Oral Microbiol Immunol 18:104-108, 2003.

Jacinto RC, Gomes BPFA, Ferraz CCR, Zaia AA, Souzafilho FJ.:

Microbiological analysis of infected root canals from symptomatic and

asymptomatic teeth with periapical periodontitis and the antimicrobial

susceptibility of some isolated anaerobic bacteria. Oral Microbiol Immun

18: 285-292, 2003.

27

Sabeti M, Simon JH, Nowzari H, Slot J.:Cytomegalovirus and Epstein-Barr

virus active infection in periapical lesions of teeth with ions intact crowns. J

Endodo 29:321-323, 2003.

Sabeti M, Simon JH, Slots J.:Cytomegalovirus and Epstein-Barr virus are

associated with symptomatic periapical pathosis. Oral Microbiol Immunol

18 327-328, 2003.

Slots J, Sabeti M, Simon JH: Herpesviruses in periapical pathosis: An

etiopathogenic relationshipO Oral Surg Oral med O 96:327-331, 2003.

Happonen RP, Bergenholtz G: Apical periodontitis. In: Bergenholtz G,

Horsted-Bindlev P, Reit C (eds.): Textbook of Endodontology. Blackwell

Publ. Ltd., Oxford, 2003, pp. 130-144

Rotstein I, Simon JHS: Diagnosis, prognosis and decision-making int he

treatment of combined periodontal-endodontic lesions. Periodontology 2000

34:165-203, 2004.

Slots J, Nowzari H, Sabeti M: Cytomegalovirus infection in symptomatic

periapical pathosis Int Endod J 37:519-524, 2004.

Kawahara T, Murakami S, Noiri Y, Ehara A, Takemura N, Furukawa S,

Ebisu S: Effects of cyclosporin-A-induced immunosuppression on

periapical lesions in rats. J Dent Res 83:683-687, 2004.

Asfora KK, Santos MDMD, Montes MAJR, Machado CM, de Castro B:

Evaluation of biocompatibility of sodium perborate and 30% hydrogen

peroxide using the analysis of the adherence capacity and morphology of

macrophages. J Dent 33:155-162, 2005.

Kabak SL, Kabak YS, Anischenko SL: Light microscopic study of

periapical lesions associated with asymptomatic apical periodontitis. Annals

of Anatomy-Anatomischer Anzeiger 187:185-194, 2005.

Quesnell BT, Alves M, Hawkinson RW, Johnson BR, Wenckus CS, BeGole

EA: The effect of human immunodeficiency virus on endodontic treatment

outcome. J Endod 31: 633-636, 2005.

Yamasaki M, Morimoto T, Tsuji M, Akihiro I, Maekawa Y, Nakamura H:

Role of IL-2 and helper T-lymphocytes in limiting periapical pathosis.

J Endod 32: 24-29, 2006.

Vernal R, Dezerega A, Dutzan N, Chaparro A, Leon R, Chandia S, Silva A,

Gamonal J: RANKL in human periapical granuloma: possible involvement

in periapical bone destruction. Oral Dis 12: 283-289, 2006.

Tözüm, T.F., Şençimen, M., Ortakoǧlu, K., Özdemir, A., Aydin, O.C.,

Keleş, M: Diagnosis and treatment of a large periapical implant lesion

associated with adjacent natural tooth: A case report. Oral Surg, Oral Med,

Oral Pathol, Oral Radiol Endod 101:132-138, 2006.

28

Slots J, Saygun I, Sabeti M, Kubar A: Epstein-Barr virus in oral diseases. J

Periodont Res 41: 235-244, 2006.

Lukic A, Vasilijic S, Majstorovic I, Vucevic D, Mojsilovic S, Gazivoda D,

Danilovic V, Petrovic R, Colic M: Characterization of antigen-presenting

cells in human apical periodontitis lesions by flow cytometry and

immunocytochemistry. Int Endod J 39: 626-636, 2006.

Menezes R, Bramante CM, Paiva KBD, Letra A, Carneiro E, Zambuzzi

WF, Granjeiro JM: Receptor activator NF kappa B-ligand and

osteoprotegerin protein expression in human periapical cysts and

granulomas. Oral Surg Oral Med Oral Pathol Oral Radiol Endod

102: 404-409, 2006.

Shetty, K., Garcia, J., Leigh, J: Success of root canal therapy in HIV-

positive patient. General Dent 54:397-402, 2006.

Colic M, Lukic A, Vucevic D, Milosavljevic P, Majstorovic I, Marjanovic

M, Dimitrijevic J: Correlation between phenotypic characteristics of

mononuclear cells isolated from human periapical lesions and their in vitro

production of Th1 and Th2 cytokines. Arch Oral Biol 51: 1120-1130, 2006.

Jankowska-Antczak, E., Włodarski, K., Wojtowicz, A: Evaluation of

immunosuppressive therapy inf

okołowierzchołkowych po przeszczepieniach narzadowych].

Implantoprotetyka 7:2-6, 2006.

Huth KC, Saugel B, Jakob FM, Cappello C, Quirling M, Paschos E, Ern K,

Hickel R, Brand K: Effect of aqueous ozone on the NF-kappa B system. J

Dent Res 86: 451-456, 2007.

Santos, L.C., Ramos, E.A.G., Gurgel, C.A.S., De Santana, E.J.B., Dos

Santos, J.N: Immunohistochemical detection of Langerhans cells in dental

granulomas and radicular cyst. J Mol Histol 38:201-205, 2007.

Rezende TMB, Vieira LQ Cardoso FP, Oliveira RR, de Oliveira Mendes ST

Jorge MLR, Ribeiro AP The effect of mineral trioxide aggregate on

phagocytic activity and production of reactive oxygen, nitrogen species and

arginase activity by M1 and M2 macrophages.Int Endod J 40: 603-611,

2007.

Andric M, Milasin J, Jovanovic T, Todorovic L: Human cytomegalovirus is

present in odontogenic cysts. Oral Microbiol Immunol 22: 347-351, 2007.

Saboia-Dantas CJ, de Toledo LFC, Sampaio-Filho HR, Siqueira JF:

Herpesviruses in asymptomatic apical periodontitis lesions: an

immunohistochemical approach. Oral Microbiol Immunol 22: 320-325,

2007.

29

Martinez ZRA, Naruishi K, Yamashiro K, Myokai F, Yamada T, Matsuura

K, Namba N, Arai H, Sasaki J, Abiko Y, Takashiba S: Gene profiles during

root canal treatment in experimental rat periapical lesions. J Endod 33: 936-

943, 2007.

Takeichi O, Hama S, Iwata K, Ito K: Confocal immunolocalization of VE-

cadherin- and CXC chemokine-expressing endothelial cells in periapical

granulomas. Internatl Endod J 41: 401-407, 2008.

Sassone LM, Fidel RA, Faveri M, Guerra R, Figueiredo L, Fidel SR, Feres

M: A microbiological profile of symptomatic teeth with primary endodontic

infections. J Endod 34: 541-545, 2008.

Lukic A, Danilovic V, Petrovic R: Comparative immunohistochemical and

quantitative analysis of inflammatory cells in symptomatic and

asymptomatic chronic periapical lesions. Vojnosanit Pregl 65:435-440,

2008.

Yazdi KA, Sabeti M, Jabalameli F, Eini ME, Kolahdouzan SA, Slots J:

Relationship between human cytomegalovirus transcription and

symptomatic apical periodontitis in Iran. Oral Microbiol Immunol 23:510-

514, 2008.

Carneiro E, Menezes R, Garlet GP, Garcia RB, Bramante CM, Figueira R,

Sogayar M, Granjeiro JM: Expression analysis of matrix metalloproteinase-

9 in epithelialized and nonepithelialized apical periodontitis lesions . Oral

Surg Oral Med Oral Pat Oral Radiol Endod 107: 127-132, 2009.

Hren NI, Ihan A: T lymphocyte activation and cytokine expression in

periapical granulomas and radicular cysts. Arc Oral Biol 54:156-161, 2009.

Corotti MV, Zambuzzi WF, Paiva KBS, Menezes R, Pinto LC, Lara VS,

Granjeiro JM: Immunolocalization of matrix metalloproteinases-2 and-9

during apical periodontitis development. Arc Oral Biology 54: 764-771,

2009.

Gazivoda D, Dzopalic T, Bozic B, Tatomirovic Z, Brkic Z, Colic M:

Production of proinflammatory and immunoregulatory cytokines by

inflammatory cells from periapical lesions in culture. J Oral Pathol Med 38:

605-611, 2009.

Saito D, Marsh TL, Cannavan FD, Hofling JF, Goncalves RB: Assessment

of intraradicular bacterial composition by terminal restriction fragment

length polymorphism analysis. Oral Microbiol Immunol 24:369-376, 2009.

Latoo, S., Shah, A.A., Jan, S.M., Qadir, S., Ahmed, I., Purra, A.R., Malik,

A.H: Radicular cys. JK Science 11:187-189, 2009.

de Paula-Silva FWG, D'Silva NJ, da Silva LAB, Kapila YL: High Matrix

Metalloproteinase Activity Is a Hallmark of Periapical Granulomas. J

35:1234-1242, 2009.

30

De Brito LCN, da Rosa MAC, Lopes VS, Ferreira EFE, Vieira LQ,

Sobrinho APR: Brazilian HIV-Infected Population: Assessment of the

Needs of Endodontic Treatment in the Post-Highly Active Antiretroviral

Therapy Era. J Endod 35:1178-1181, 2009.

Colic M, Gazivoda D, Vucevic D, Majstorovic I, Vasilijic S, Rudolf R,

Brkic Z, Milosavljevic P: Regulatory T-cells in Periapical Lesions.J Dent

Res 88:997-1002, 2009.

Buzoglu HD, Unal H, Ulger C, Mert S, Kucukyildirim S, Er N: The

zymographic evaluation of gelatinase (MMP-2 and-9) levels in acute and

chronic periapical abscesses. Oral Surg Oral Med Oral Pathol Oral Radiol

Endodont 108:e121-e126, 2009.

Colic M, Gazivoda D, Vucevic D, Vasilijic S, Rudolf R, Lukic A:

Proinflammatory and immunoregulatory mechanisms in periapical lesions.

Mol Immunol 47:101-113, 2009.

Colic M, Gazivoda D, Majstorovic I, Dragicevic A, Vasilijic S, Rudolf R,

Milosavljevic P, Vucevic D: Immunomodulatory Activity of IL-27 in

Human Periapical Lesions. J Dent Res 88:1142-1147, 2009.

Tsuji M, Yamasaki M, Amano K, Matsui H, Morimoto T, Nakamura H:

Histochemical localization of neutral proteases released during development

of rat periradicular lesion. Arch Oral Biol 54:1128-1135, 2009.

Paula-Silva, F.W.G., da Silva, L.A.B., Kapila, Y.L: Matrix

Metalloproteinase Expression in Teeth with Apical Periodontitis Is

Differentially Modulated by the Modality of Root Canal Treatment. J Endod

36:231-237, 2010.

Drazic R, Sopta J, Minic AJ: Mast cells in periapical lesions: potential role

in their pathogenesis. J Oral Pathol Med 39:257-262, 2010.

Mathew, S., Yaw-Chyn, L., Kishen, A: Immunogenic Potential of

Enterococcus faecalis Biofilm under Simulated Growth Conditions. J Endod

36:832-836, 2010.

Paula-Silva FWG, da Silva LAB, Kapila YL: Matrix Metalloproteinase

Expression in Teeth with Apical Periodontitis Is Differentially Modulated

by the Modality of Root Canal Treatment. J Endod 36:231-237, 2010.

Marcal JRB, Samuel RO, Fernandes D, de Araujo MS, Napimoga MH,

Pereira SAL, Clemente-Napimoga JT, Alves PM, Mattar R, Rodrigues V,

Rodrigues DBR: T-Helper Cell Type 17/Regulatory T-Cell

Immunoregulatory Balance in Human Radicular Cysts and Periapical

Granulomas. J Endod 36:995-999, 2010.

Lee YL, Lin SK, Hong CY, Wang JS, Yang H, Lai EHH, Chen MH, Kok

SH: Major Histocompatibility Complex Class II Transactivator Inhibits

Cysteine-rich 61 Expression in Osteoblastic Cells and Its Implication in the

Pathogenesis of Periapical Lesions. J Endod 36:1021-1025, 2010.

31

Paula-Silva FWG, Ghosh A, Arzate H, Kapila S, da Silva LAB, Kapila YL:

Calcium Hydroxide Promotes Cementogenesis and Induces Cementoblastic

Differentiation of Mesenchymal Periodontal Ligament Cells in a CEMP1-

and ERK-Dependent Manner :Calcified Tissue International 87:144-157,

2010.

Ad Hegedűs C, Flóra-Nagy E, Martos R, Juhász A, Fülöp I, Pomaházi S, Nagy

IP, Tóth Z, Márton I, Keszhelyi G: Simplified 3D reconstruction based on

hard tissue microtome cross section pictures in dentistry. Computer

Methods and Programs in Biomedicine 63:77-84, 2000. (1)

Khooshabeh P, Hegarty M.; Inferring cross-sections: When internal

visualizations are more important than properties of external visualizations.

Human-Computer Interaction 25:119-147, 2010.

Ad Radics T, Tar I, Bágyi K, Márton I: A periapikális léziók típusainak

prevalenciája, a szövettani értékelés jelentősége. Fogorv Szle 93:108-114,

2000. ( )+1

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Ad Redl P, Gyulaházi J, Kiss C, Márton I: Fibromatosis in the paramandibular

region. Med Pediatr Oncol 37:75-76, 2001. (1)

Lackner H, Urban C, Benesch M, Raith J, Moser A, Sovinz P, Schwinger

W, Dornbusch HJ, Triebl-Roth K: Multimodal treatment of children with

unresectable or recurrent desmoid tumors: An 11-year longitudinal

observational study . J of Ped Hematol Oncol 26:518-522, 2004.

Ad Juhász A, Szabó Z, Márton I, Fejérdy P, Dobó Nagy Cs: A gyökércsatorna

morfológiai hatása a mikroszivárgás mértékére. Fogorv Szle 95: 27-31,

2002. (2)+1

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

J.J.G. Calvo: Estudio in vitro del sellado de conductos obturados con

gutapercha y sellador AH26 mediante la technica de la condensatión laterale

de la gutapercha en frío. Tesis, Universitat de Valencia, 2006.

32

Nemes J, Duhaj Sz, Nyárasdy 1. A fogbélbetegségek és a fogbél

következményes betegségeinek terápiájában (gyökérkezelés) bekövetkezett változások 100 éve a Fogorovsi Szemle közleményeinek tükrében. Fogorv

Szle 101:127-136, 2008.

Ad Radics T, Kiss C, Tar I, Márton IJ: Interleukin-6 and GM-CSF in apical

periodontitis: correlation with clinical and histologic findings of the

involved teeth. Oral Microbiol Immunol 18:9-13, 2003. (9)+1

Márton 1. Immun és lobos folyamatok szerepe a szájüreg

megbetegedéseiben, különös tekintettel az idült apikális periodontitisre.

MTA Doktori Tézisek, Debreceni Egyetem, OEC, Fogorvostudományi

Intézet, Debrecen, 2002.

Slots J, Sabeti M, Simon JH: herpesviruses in periapical pathosis: An

etiopathogenic relationship. Oral Surg Oral Med Oral Pathol Oral Radiol

Endod 96:327-331, 2003.

Slots J, Nowzari H, Sabeti M: Cytomegalovirus infection in symptomatic

periapical pathosis Int Endod J 37:519-524, 2004.

Vernal R, Dezerega A, Dutzan N, Chaparro A, Leon R, Chandia S, Silva A,

Gamonal J: RANKL in human periapical granuloma: possible involvement

in periapical bone destruction. Oral Dis 12:283-289, 2006.

Meurman, J.H., Hämäläinen, P., Janket, S.-J: Oral infections in older adults.

Aging Health 2:1013-1023, 2006.

Prso IB, Kocjan W, Simic H, Brumini G, Pezelj-Ribaric S, Borcic J, Ferreri

S, Karlovic IM: Tumor necrosis factor-alpha and interleukin 6 in human

periapical lesions. Mediators of Inflammation Art. No. 38210, 2007.

Brekalo Prso, I., Kocjan, W., S , H., Brumini, G., - , S.,

Borc , J., Ferreri, S. , I: Tumor necrosis factor-alpha and

interleukin 6 in human periapical lesions. Mediat Inflamm 2007, art. no.

38210, 2007.

Bolan M, Lima DD, Figueiredo CP, Di Giunta G, Rocha MJD:

Immunohistochemical Study of Presence of T Cells, B Cells, and

Macrophages in Periradicular Lesions of Primary Teeth. J Clin Pediatr Dent

32:287-293, 2008.

Colic M, Gazivoda D, Vucevic D, Vasilijic S, Rudolf R, Lukic A:

Proinflammatory and immunoregulatory mechanisms in periapical lesions.

Molecular Immunology Volume: 47:101-113, 2009.

Dezerega A, Osorio C, Mardones J, Mundi V, Dutzan N, Franco M,

Gamonal J, Oyarzún A, Overall C.M, Hernández M: Monocyte chemotactic

protein-3: Possible involvement in apical periodontitis chemotaxis. Int

Endod J 43:902-908, 2010.

33

Ad Alberth M, Kovalecz G, Török J, Nemes J, Kiss C, Marton IJ: Oral health

of long-term childhood cancer survivors. Pediatr Blood Cancer (Med

Pediatric Oncol) 43: 88-90, 2004. (6)

Dickerman JD: The late effects of childhood cancer therapy. Pediatrics

119:554-568, 2007.

Avsar A, Elli M, Darka O, Pinarli G: Long-term effects of chemotherapy on

caries formation, dental development, and salivary factors in childhood

cancer survivors. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 104:

781-789, 2007.

Hong, C.H., daFonseca, M: Considerations in the Pediatric Population with

Cancer. Dent Clin North America 52:155-181, 2008.

Goncalves MIR, Radzinsky TC, da Silva NS, Chiari BM, Consonni D:

Speech-language and hearing complaints of children and adolescents with

brain tumors. Pediatr Blood Cancer 50: 706-708, 2008.

Hobbie WL, Moshang T, Carlson CA, Goldmuntz E, Sacks N, Goldfarb SB,

Grupp SA, Ginsberg JP: Late effects in survivors of tandem peripheral

blood stem cell transplant for high-risk neuroblastoma. Pediatr Blood &

Cancer 51:679-683, 2008.

Gorin, S.S., McAuliffe, P: Implications of childhood cancer survivors in the

classroom and the school. Health Educat 109:25-48, 2009.

Ad Márton IJ: How does the periapical inflammatory process compromise

general health? Endodontic Topics 8:3-14, 2004. (1)

Carrotte P: 21st Century endodontics - Part 5. Int Dent J 55:388-394, 2005.

Ad Szládek G, Juhász A, Kardos G, Szőke K, Major T, Sziklai I, Tar I,

Márton I, Konya J, Gergely L, Szarka K: High co-prevalence of genogroup

1 TT virus and human papillomavirus associated with poor clinical outcome

of laryngeal carcinoma. J Clin Pathol 58:402-405, 2005. (9)

Abraham P: TT viruses: How much do we know? Ind J Med Res 122: 7-10,

2005.

Irshad M, Joshi YK, Sharma Y, Dhar I: Transfusion transmitted virus: A

review on its molecular characteristics and role in medicine. World J

Gastroenterol 12:5122-5134, 2006.

Gergely P, Perl A, Poor G: Possible pathogenic nature of the recently

discovered TT virus: Does it play a role in autoimmune rheumatic diseases?

Autoimmunity Rev 6:5-9, 2006.

Hu YW, Al-Moslih MI, Al Ali MT, Uzicanin S, Perkins H, Yi QL,

Khameneh SR, Wu J, Brown EG: Clinical outcome of frequent exposure to

34

Torque Teno virus (TTV) through blood transfusion in thalassemia patients

with or without hepatitis C virus (HCV) infection. J Med Virol 80:365-371,

2008.

Blazsek A, Sillo P, Ishii N, Gergely P, Poor G, Preisz K, Hashimoto T,

Medvecz M, Karpati S: Searching for foreign antigens as possible triggering

factors of autoimmunity: Torque Teno virus DNA prevalence is elevated in

sera of patients with bullous pemphigoid. Exp Dermatol 17:446-454, 2008.

Davidson I, Shulman LM: Unraveling the puzzle of human anellovirus

infections by comparison with avian infections with the chicken anemia

virus. Virus Research 137:1-15, 2008.

Okamoto H: History of discoveries and pathogenicity of TT viruses. Cur

Topics Microbiol Immunol 33:1-20, 2009.

Fehér E, Gáll T, Murvai M, Kis A, Boda R, Sápy T, Tar I, Gergely L,

Szarka K: Investigation of the occurrence of torque tenovirus in malignant

and potentially malignant disorders associated with human papillomavirus J

Med Virol 81:1975-1981, 2009.

Roperto S, Paciello O, Paolini F, Pagnini U, Palma E, di Palo R, Russo V,

Roperto F, Venuti A: Detection of human torque teno virus in the milk of

water buffaloes (Bubalus bubalis). J Dairy Sci 92:5928-5932, 2009.

Ad Nemes JA, Nemes Z, Márton IJ: P21WAF1/CIP1 Expression is a Marker

of Poor Prognosis in Oral Squamous Cell Carcinoma. J Oral Pathol Med 34:

274-279, 2005. (12)

Stehr W, Bernal NP, Erwin CR, Bernabe KQ, Guo J, Warner BW: Roles for

p21(waf1/cip1) and p27(kip1) during the adaptation response to massive

intestinal resection. Am J Physiol-Gastr L 290: G933-G941, 2006.

Galmozzi F, Rubagotti A, Romagnoli A, Carmignani G, Perdelli L,

Gatteschi B, Boccardo F: Prognostic value of cell cycle regulatory proteins

in muscle-infiltrating bladder cancer. J Canc Res Clin Oncol 132: 757-764,

2006.

Horta MCR, Assis LAP, Souza AF, de Araujo VC, Gomez RS, Aguiar

MCF: p53 and p21(WAF1/CIP1) overexpression at the invasive front of

lower lip squamous cell carcinoma. J Oral Pathol Med 36: 88-92, 2007.

Gomes CC, Drummond SN, Guimaraes ALS, Andrade CI, Mesquita RA,

Gomez RS: P21/WAF1 and cyclin D1 variants and oral squamous cell

carcinoma. J Oral Pathol Med 37:151-156, 2008.

Martinez A, Brethauer U, Borlando J, Spencer ML, Rojas IG: Epithelial

expression of p53, mdm-2 and p21 in normal lip and actinic cheilitis. Oral

Oncol 44:878-883, 2008.

Marques YMFS, de Lima MDM, Alves SD, Soares FA, de Araujo VC,

Pinto DD, Mantesso A: Mdm2, p53, p21 and pAKT protein pathways in

35

benign neoplasms of the salivary gland. Oral Oncol 44:903-908, 2008.

Colombo J, Fachel AA, Calmon MD, Cury PM, Fukuyama EE, Tajara EH,

Cordeiro JA, Verjovski-Almeida S, Reis EM, Rahal P: Gene expression

profiling reveals molecular marker candidates of laryngeal squamous cell

carcinoma. Oncol Rep 21: 649-663, 2009.

van den Broek GB, Wildeman M, Rasch CRN, Armstrong N, Schuuring E,

Begg AC, Looijenga LHJ, Scheper R, van der Wal JE, Menkema L, van

Diest PJ, Balm AJM, van Velthuysen MLF, van den Brekel MWM:

Molecular markers predict outcome in squamous cell carcinoma of the head

and neck after concomitant cisplatin-based chemoradiation. Internat J

Cancer 124:2643-2650, 2009.

de Lima MDM, Marques YMFS, Alves SD, Freitas VM, Soares FA, de

Araujo VC, Pinto DD, Mantesso A: MDM2, P53, P21(WAF1) and pAKT

protein levels in genesis and behaviour of adenoid cystic carcinoma. Cancer

Epidemiol 33:142-146, 2009.

Wu, J.-Y., Yi, C., Chung, H.-R., Wang, D.-J., Chang, W.-C., Lee, S.-Y.,

Lin, C.-T., Yang, Y.-C., Yang, W.-C.V: Potential biomarkers in saliva for

oral squamous cell carcinoma. Oral Oncol 46:226-231, 2010.

Ribeiro, D.A., Nascimento, F.D., Fracalossi, A.C.C., Gomes, T.S., Oshima,

C.T.F., Franco, M.F: Expression profiling of cell cycle regulatory proteins

in oropharyngeal carcinomas using tissue microarrays. In Vivo 24:315-320,

2010.

Mishra, R.: Glycogen synthase kinase 3 beta: Can it be a target for oral

cancer. Molecular Cancer 9, art. no. 144, 2010.

Ad Nemes JA, Deli L, Nemes Z, Márton IJ: Expression of p 16INK4A

, p53, and

Rb proteins are independent from the presence of human papillomavirus

genes in oral squamous cell carcinoma. Surg Oral Med Oral Pathol Oral

Radiol Endod 102: 344-352, 2006. (15)

O'Regan EM, Toner ME, Finn SP , Fan CY, Ring M, Hagmar B, Timon C,

Smyth P, Cahill S, Flavin R, Sheils OM, O'Leary JJ: p16(INK4A) genetic

and epigenetic profiles differ in relation to age and site in head and neck

squamous cell carcinomas. Human Pathology 39:452-458, 2008.

Takeshima M, Saitoh M, Kusano K, Nagayasu H, Kurashige Y, Malsantha

M, Arakawa T, Takuma T, Chiba I, Kaku T, Shibata T, Abiko Y: High

frequency of hypermethylation of p14, p15 and p16 in oral pre-cancerous

lesions associated with betel-quid chewing in Sri Lanka. J Oral Pathol Med

37:475-479, 2008.

Termine N Panzarella V, Falaschini S, Russo A, Matranga D, Lo Muzio L,

Campisi G: HPV in oral squamous cell carcinoma vs head and neck

squamous cell carcinoma biopsies: a meta-analysis. Annals of Oncology

19:1681-1690, 2008.

36

Simonato LE, Garcia JF, Sundefeld MLMM, Mattar NJ, Veronese LA,

Miyahara GI: Detection of HPV in mouth floor squamous cell carcinoma

and its correlation with clinicopathologic variables, risk factors and survival.

J Oral Pathol Med 37: 593-598, 2008.

Soares RC, Oliveira MC, de Souza LB, Costa ADL, Pinto LP: Detection of

hpv dna and immunohistochemical expression of cell cycle proteins in oral

carcinoma in a population of brazilian patients. J Applied Oral Sci 16:340-

344, 2008.

Oliveira LR, Ribeiro-Silva A, Ramalho LNZ, Simoes AL, Zucoloto S: HPV

infection in Brazilian oral squamous cell carcinoma patients and its

correlation with clinicopathological outcomes. Molecul Med Rep 1:123-

129, 2008.

Buajeeb W, Poomsawat S, Punyasingh J, Sanguansin S:Expression of p16 in

oral cancer and premalignant lesions. J Oral Pathol Med 38: 104-108, 2009.

Oliveira MC, Soares RC, Pinto LP, de Souza LB, de Medeiros SRB, Costa

ADL: High-risk human papillomavirus (HPV) is not associated with p53

and bcl-2 expression in oral squamous cell carcinomas. Auris Nasus 36:450-

456, 2009.

Ribeiro DA, Fracalossi ACC, Uatari SA, Oshima CTF, Salvadori DMF:

Imbalance of Tumor Suppression Genes Expression Following Rat Tongue

Carcinogenesis Induced by 4-Nitroquinoline 1-Oxide. In Vivo 23:937-942,

2009.

Feller, L., Khammissa, R.A., Wood, N.H., Lemmer, J: Epithelial maturation

and molecular biology of oral HPV. Infect Agents Cancer 4:16, 2009.

Ferreira, D.D.C., Curvelo, J.A., Passos, M.R: Open questions on

carcinogenesis of oral cancer: Interaction between the environmental and

genetic aspects. Ind J Dent Res 20:249, 2009.

St Guily, J.L., Clavel, C., Agius, G: Papillomavirus and tumors of the upper

gastrointestinal tracts (except juvenile papillomatosis) | [Papillomavirus et

tumeurs des voies aérodigestives supérieures (hors papillomatose juvénile)].

Med Therap Ped 13:62-69, 2010.

Brandwein-Gensler, M., Smith, R.V: Prognostic indicators in head and neck

oncology including the New 7th edition of the AJCC staging system. Head

Neck Pathol 4:53-61, 2010.

Mohseni Mehran, S.M: Detection of Human Papilloma Virus in Esophageal

Squamous Cell Carcinoma in Guilan province. J Clin Diagn Res 4:2373-

2377, 2010.

Friedrich RE, Sperber C, Jäkel T, Röser K, Löning T: Basaloid lesions of

oral squamous epithelial cells and their association with HPV infection and

P16 expression. Anticancer Research 30:1605-1612, 2010.

37

Ad Bágyi K, Klekner Á, Hutóczki G, Márton I: A szájüregi baktériumok

szerepe az aspirációs pneumónia patogenezisében. Fogorv Szle 99:205-

212, 2006. (1)

Gomes-Filho, I.S., Santos, C.M.L., Cruz, S.S., Passos, J.D.S., Cerqueira,

E.D.M.M., Costa, M.D.C.N., Santana, T.C., (...), Barreto, M.L: Periodontitis

and nosocomial lower respiratory tract infection: Preliminary findings.

Journal of Clinical Periodontology 36:380-387, 2009.

Ad Nemes J, Boda R, Redl P, Márton I: Szájüregi laphámrákok vizsgálata II.

(etiológiai faktorok) Fogorv Szle 99:179-185, 2006. (1)

Scardina, G.A., Messina, P: Nutrition and oral health | [Alimentazione e

salute del cavo orale]. Rec Progr Med 99:106-111, 2008.

Ad Alberth M, Majoros L, Kovalecz G, Szegedi I, Márton I, Kiss C:

Significance of oral Candida infections in Children with cancer. Pathol

Oncol Res 12: 237-241, 2006. (6)

Parahym, A.M.R.C., de Melo, L.R.B., de Morais, V.L.L., Neves, R.P:

Candidiasis in pediatric patients with cancer interned in a university hospital

[Candidíases em pacientes pediátricos com cancer internados em um

hospital universitário]. Brazil J Microbiol 40:321-324, 2009.

Bailey LC, Reilly AF, Rheingold SR: Source: Infections in Pediatric

Patients With Hematologic Malignancies. Seminars Hematol 46: 313-324,

2009.

Sobol, G., Mizia-Malarz, A., Musioł, K., Krupa, M., Stolpa, W., Szyszka,

A., Walczak, E., Woś, H: Invasive fungal infection in children with

neoplasms - Single institution experience [Inwazyjne zakażenia grzybicze u

dzieci z choroba nowotworowa z uwzglȩdnieniem doświadczeń własnych].

Mikolog Lekars 16:67-71, 2009.

Tsang, P.W.-K., Wong, K.-S., Chu, J.K.-M: Isolation and characterization

of Candida kefyr orotidine-5′- phosphate decarboxylase (URA3) gene.

Yeast 27:53-58, 2010.

Ponce-Torres E, Ruíz-Rodríguez MDS, Alejo-González F, Hernández-

Sierra JF, De Pozos-Guillén AD: Oral manifestations in pediatric patients

receiving chemotherapy for acute lymphoblastic leukemia. J Clin Pediatric

Dent 34:275-279, 2010.

Majorana A, Bardellini E, Flocchini P, Amadori F, Conti G, Campus G:

Oral mucosal lesions in children from 0 to 12 years old: Ten years'

experience. Oral Surg, Oral Med, Oral Pathol, Oral Radiol Endodont

110:e13-e18, 2010.

38

Ad Márton I: A granuloma apicale fogorvosi és általános orvostudományi

jelentősége. Fogorv. Szle 100:193-199, 2007. (1)

Nemes J, Duhaj Sz, Nyárasdy I: A fogbélbetegségek és a fogbél

következményes betegségeinek terápiájában(gyökérkezelés) bekövetkezett

változások 100 éve a Fogorvosi Szemle közleményeinek tükrében (1908-

2008). Fogorv Szle 101:127-136, 2008.

Ad Bakó J, Szepesi M, Márton I, Borbély J, Hegedűs Cs: Fogászatban

alkalmazható hatóanyagok leadására alkalmas nanorészecskék szintézise.

Fogorv. Szle 100:109-113, 2007. (1)

Jain N, Jain GK, Javed S, Iqbal Z, Talegaonkar S, Ahmad FJ, Khar RK:

Recent approaches for the treatment of periodontitis. Drug Discovery Today

13:932-943, 2008.

Ad Szabó A, Szentandrássy N, Birinyi P, Horváth B, Szabó G, Bányász T,

Márton I, Nánási P, Magyar J: Effect of articaine on action potential

characteristics and the undelying ion currents in canine ventricular

myocytes. British J Anaesthesia 99:726-733, 2007. ( )+1

Szabó A, Szentandrássy N, Birinyi P, Horváth B, Szabó G, Bányász T,

Márton I, Magyar J, Nánási PP: Effects of articaine and ropivacaine on

calcium handling and contractility in canine ventricular myocardium. Eur J

Anaesthesiol 27:153-161, 2010.

Ad Tar I, Kiss C, Marodi L, Márton IJ: Oral and dental conditions of children

with selective IgA deficiency. Pediatric Allerg Immunol 19:33-36, 2008.(3)

Majorana, A., Cardellini, E., Saggese, V., Giuca, M.R: Pedodontist and

pediatrician in the management of the child affected by systemic pathologies

[Pedodontista e pediatra nella gestione del bambino affetto da patologie

sistemiche]. Minerva Pediatrica 60:473-479, 2008.

Gregorek H, Olczak-Kowalczyk D, Dembowska-Baginska B, Pietrucha B,

Wakulinska A, Gozdowski D, Chrzanowska KH: Oral findings in patients

with Nijmegen breakage syndrome: A preliminary study. Oral Surg Oral

Med Oral Pathol Oral Radiol Endod 108:E39-E45, 2009.

Jorgensen GH, Arnlaugsson S, Theodors A, Ludviksson BR:

Immunoglobulin A deficiency and oral health status: a case-control study. J

Clin Periodont 37:1-8, 2010.

39

Ad Nemes JA, Redl P, Boda R, Kiss C, Marton IJ: Oral cancer report from

North Eastren Hungary. Pathol Oncol Res 14:85-92, 2008. (1)

Lira, R.C.P., Miranda, F.A., Guimarães, M.C.M., Simões, R.T., Donadi,

E.A., Soares, C.P., Soares, E.G: BUBR1 expression in benign oral lesions

and squamous cell carcinomas: Correlation with human papillomavirus.

Oncology Rep 23:1027-1036, 2010.

Ad Szabó A, Szentandrássy N, Birinyi P, Horváth B, Szabó G, Bányász T,

Márton I, Magyar J, Nánási PP: Effects of ropivacaine on action potential

configuration and ion currents in isolated canine ventricular

cardiomyocytes. Anesthesiology 108: 693-702, 2008. (1)+1

Szabó A, Szentandrássy N, Birinyi P, Horváth B, Szabó G, Bányász T,

Márton I, Magyar J, Nánási PP: Effects of articaine and ropivacaine on

calcium handling and contractility in canine ventricular myocardium. Eur

J Anaesthesiol 27:153-161, 2010.

Butterworth JF: Models and mechanisms of local anesthetic cardiac

toxicity: A review. Reg Anesth Pain Med 35:167-176, 2010.

Ad Marincsák R, Tóth BI, Czifra G, Márton I, Redl P, Tar I, Tóth L, Kovács

L, Bíró T: Increased expression of TRPVI in squamous cell carcinoma of

the human tongue. Oral Diseases 15:328-335, 2009. (1)

Ding X, He Z, Shi Y, Wang Q, Wang Y: Targeting TRPC6 channels in

oesophageal carcinoma growth. Expert Opinion on Therapeutic Targets

14:513-527, 2010.

Ad Szarka K, Tar I, Fehér E, Kis A, D Tóth E, Boda R, Márton I, Gergely L:

Progressive increase of human paillomavirus carriage rates in potentially

malignant and malignant oral disorders with incresing malignant potential.

Oral Microbiol Immunol 24:314-318, 2009. (2)

Fehér E, Gáll T, Murvai M, Kis A, Boda R, Sápy T, Tar I, Gergely L,

Szarka K: Investigation of the occurrence of torque tenovirus in malignant

and potentially malignant disorders associated with human papillomavirus. J

Med Virol 81:1975-1981, 2009.

Slots J: Human viruses in periodontitis. Periodontology 2000:89-110, 2010.

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