These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 23091740)

  • 1. Amelogenesis imperfecta and generalized gingival overgrowth resembling hereditary gingival fibromatosis in siblings: a case report.
    Yaprak E; Subaşı MG; Avunduk M; Aykent F
    Case Rep Dent; 2012; 2012():428423. PubMed ID: 23091740
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Amelogenesis imperfecta and unusual gingival hyperplasia.
    Macedo GO; Tunes RS; Motta AC; Passador-Santos F; Grisi MM; Souza SL; Palioto DB; Taba M; Novaes AB
    J Periodontol; 2005 Sep; 76(9):1563-6. PubMed ID: 16171448
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary gingival fibromatosis associated with generalized aggressive periodontitis: a case report.
    Casavecchia P; Uzel MI; Kantarci A; Hasturk H; Dibart S; Hart TC; Trackman PC; Van Dyke TE
    J Periodontol; 2004 May; 75(5):770-8. PubMed ID: 15212361
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary gingival hyperplasia associated with amelogenesis imperfecta: a case report.
    Nibali L; Brett PM; Donos N; Griffiths GS
    Quintessence Int; 2012 Jun; 43(6):483-9. PubMed ID: 22532955
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
    Cherkaoui Jaouad I; El Alloussi M; Chafai El Alaoui S; Laarabi FZ; Lyahyai J; Sefiani A
    BMC Oral Health; 2015 Jan; 15():14. PubMed ID: 25636655
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case reports of a new syndrome associating gingival fibromatosis and dental abnormalities in a consanguineous family.
    Martelli-Júnior H; Bonan PR; Dos Santos LA; Santos SM; Cavalcanti MG; Coletta RD
    J Periodontol; 2008 Jul; 79(7):1287-96. PubMed ID: 18597613
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Generalized hereditary gingival fibromatosis in a child: clinical, histopathological and therapeutic aspects.
    Cunha JLS; Ramos MACDC; Regis DM; Sanchéz-Romero C; de Andrade ME; Bezerra BT; de Albuquerque-Júnior RLC
    Autops Case Rep; 2020; 10(1):e2020140. PubMed ID: 32039068
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enamel-renal-gingival syndrome and FAM20A mutations.
    Kantaputra PN; Kaewgahya M; Khemaleelakul U; Dejkhamron P; Sutthimethakorn S; Thongboonkerd V; Iamaroon A
    Am J Med Genet A; 2014 Jan; 164A(1):1-9. PubMed ID: 24259279
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary Gingival Fibromatosis: A Report of a Rare Case in Siblings and Its Management Using Diode Laser.
    Dureja D; Sharma H; Agarwal M; Srivastava S; Tandon P
    Contemp Clin Dent; 2020; 11(3):290-293. PubMed ID: 33776359
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gingival Fibromatosis with Distinctive Facies - A Three Generation Case Report.
    Kanagotagi S; Sidana S; Rajguru S; Padhye A
    J Clin Diagn Res; 2015 May; 9(5):ZD05-7. PubMed ID: 26155576
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Treatment and two-year follow-up of a patient with hereditary gingival fibromatosis.
    Bansal A; Narang S; Sowmya K; Sehgal N
    J Indian Soc Periodontol; 2011 Oct; 15(4):406-9. PubMed ID: 22368369
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Autosomal Dominant Inheritance of Hereditary Gingival Fibromatosis: A Case Report.
    Karthikeyan BV; Khanna D; Prabhuji MLV
    N Y State Dent J; 2016 Nov; 82(6):43-46. PubMed ID: 30512259
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Enamel renal syndrome with associated amelogenesis imperfecta, nephrolithiasis, and hypocitraturia: A case report.
    Bhesania D; Arora A; Kapoor S
    Imaging Sci Dent; 2015 Sep; 45(3):181-5. PubMed ID: 26389061
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multispeciality approach in the management of patient with hereditary gingival fibromatosis: 1-year followup: a case report.
    Ramakrishnan T; Kaur M
    Int J Dent; 2010; 2010():575979. PubMed ID: 21234408
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nonsyndromic hereditary gingival fibromatosis: Characterization of a family and review of genetic etiology.
    Resende EP; Xavier MT; Matos S; Antunes AC; Silva HC
    Spec Care Dentist; 2020 May; 40(3):320-328. PubMed ID: 32413193
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Management of gingival overgrowth associated with generalized enamel defects in a child.
    Brennan MT; O'Connell BC; Rams TE; O'Connell AC
    J Clin Pediatr Dent; 1999; 23(2):97-101. PubMed ID: 10204448
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary gingival fibromatosis: a case report.
    Baptista IP
    J Clin Periodontol; 2002 Sep; 29(9):871-4. PubMed ID: 12423302
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gingival inflammation, enamel defects, and tooth sensitivity in children with amelogenesis imperfecta: a case-control study.
    Quandalle C; Boillot A; Fournier B; Garrec P; DE LA Dure-Molla M; Kerner S
    J Appl Oral Sci; 2020; 28():e20200170. PubMed ID: 32997085
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Seven-year follow-up of a patient with hereditary gingival fibromatosis treated with a multidisciplinary approach: case report.
    Li N; Wang W; Sun Y; Wang H; Wang T
    BMC Oral Health; 2021 Sep; 21(1):473. PubMed ID: 34565352
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report.
    Patel A; Jagtap C; Bhat C; Shah R
    Contemp Clin Dent; 2015; 6(2):262-5. PubMed ID: 26097369
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.