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 *

139 related articles for article (PubMed ID: 23637089)

  • 21. Patient with mutation in the matrix metalloproteinase 2 (MMP2) gene - a case report and review of the literature.
    Ekbote AV; Danda S; Zankl A; Mandal K; Maguire T; Ungerer K
    J Clin Res Pediatr Endocrinol; 2014; 6(1):40-6. PubMed ID: 24637309
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Aggressive polyfibromatosis: a 10 year follow-up.
    Lee YC; Chan HH; Black MM
    Australas J Dermatol; 1996 Nov; 37(4):205-7. PubMed ID: 8961590
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Juvenile hyaline fibromatosis.
    Aldred MJ; Crawford PJ
    Oral Surg Oral Med Oral Pathol; 1987 Jan; 63(1):71-7. PubMed ID: 2433666
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Report of a case of Zimmermann-Laband syndrome with new manifestations.
    Lin Z; Wang T; Sun G; Huang X
    Int J Oral Maxillofac Surg; 2010 Sep; 39(9):937-41. PubMed ID: 20457511
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [An unusual polyfibromatosis (atypical Dupuytren-Ledderhose disease, fibroma of the mouth mucosa, "epilepsy")].
    Friedrich W; Korting GW
    Dermatol Monatsschr; 1973 Dec; 159(12):1114-20. PubMed ID: 4210292
    [No Abstract]   [Full Text] [Related]  

  • 26. Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathy.
    Ishaq T; Loid P; Ishaq HA; Seo GH; Mäkitie O; Naz S
    BMC Musculoskelet Disord; 2023 Sep; 24(1):735. PubMed ID: 37710205
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hereditary gingival fibromatosis with distinctive facies.
    Prasad SS; Radharani C; Sinha S; Kumar SK
    J Contemp Dent Pract; 2012 Nov; 13(6):892-6. PubMed ID: 23404022
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review.
    Castori M; Valiante M; Pascolini G; Leuzzi V; Pizzuti A; Grammatico P
    Eur J Med Genet; 2013 Oct; 56(10):570-6. PubMed ID: 23994350
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Juvenile hyaline fibromatosis: report of a case and comparison with infantile systemic hyalinosis.
    Lim AA; Kozakewich HP; Feingold M; Padwa BL
    J Oral Maxillofac Surg; 2005 Feb; 63(2):271-4. PubMed ID: 15690301
    [No Abstract]   [Full Text] [Related]  

  • 30. Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome.
    Kasaboğlu O; Tümer C; Balci S
    Genet Couns; 2004; 15(2):213-8. PubMed ID: 15287422
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome.
    Chacon-Camacho OF; Vázquez J; Zenteno JC
    Am J Med Genet A; 2011 Jul; 155A(7):1716-20. PubMed ID: 21626675
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Oral fibromas and fibrosis. The clinical picture, histology and differential diagnosis].
    von Arx T; Hardt N; Gebbers JO
    Schweiz Monatsschr Zahnmed; 1992; 102(7):834-49. PubMed ID: 1496350
    [No Abstract]   [Full Text] [Related]  

  • 33. Facial characteristics are not distinctive features for the acrofacial dysostosis syndrome type Kennedy-Teebi.
    Ruiter M; van Dijken PJ; de Vries BB
    Am J Med Genet A; 2005 Jun; 135(3):344; author reply 345. PubMed ID: 15822074
    [No Abstract]   [Full Text] [Related]  

  • 34. Juvenile hyaline fibromatosis: a case report.
    Karaçal N; Gülçelik N; Yildiz K; Mungan S; Kutlu N
    J Cutan Pathol; 2005 Jul; 32(6):438-40. PubMed ID: 15953379
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Researchers discover gene mutation responsible for hereditary gingival fibromatosis.
    Dent Today; 2002 May; 21(5):38-9. PubMed ID: 12026713
    [No Abstract]   [Full Text] [Related]  

  • 36. Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome.
    Evans BR; Mosig RA; Lobl M; Martignetti CR; Camacho C; Grum-Tokars V; Glucksman MJ; Martignetti JA
    Am J Hum Genet; 2012 Sep; 91(3):572-6. PubMed ID: 22922033
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Two siblings with juvenile hyaline fibromatosis: case reports and review of the literature.
    Keser G; Karabulut B; Oksel F; Calli C; Ustün EE; Akalin T; Koçanaoğullari H; Gümüdiş G; Doğanavşargil E
    Clin Rheumatol; 1999; 18(3):248-52. PubMed ID: 11206353
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association of holoprosencephaly, ectrodactyly, cleft lip/cleft palate and hypertelorism: a possible third case.
    Imaizumi K; Ishii T; Masuno M; Kuroki Y
    Clin Dysmorphol; 1998 Jul; 7(3):213-6. PubMed ID: 9689997
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Acro-osteolysis, keloid like-lesions, distinctive facial features, and overgrowth: two newly recognized patients with premature aging syndrome, Penttinen type.
    Zufferey F; Hadj-Rabia S; De Sandre-Giovannoli A; Dufier JL; Leheup B; Schweitze C; Bodemer C; Cormier-Daire V; Le Merrer M
    Am J Med Genet A; 2013 Jul; 161A(7):1786-91. PubMed ID: 23720404
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Localized idiopathic gingival fibromatosis with an unusual fibroma resulting.
    Shalhoub SY
    Ann Dent; 1985; 44(2):17-9. PubMed ID: 3867321
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.