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 *

116 related articles for article (PubMed ID: 25677863)

  • 1. Pincer nail deformity as the main manifestation of Clouston syndrome.
    Hu YH; Lin YC; Hwu WL; Lee YM
    Br J Dermatol; 2015 Aug; 173(2):581-3. PubMed ID: 25677863
    [No Abstract]   [Full Text] [Related]  

  • 2. Pterygium and thinning of nails as an unusual manifestation in Clouston syndrome.
    Sukakul T; Yang HS; Onoufriadis A; Hsu CK; McGrath JA
    J Dermatol; 2019 Sep; 46(9):e329-e330. PubMed ID: 30908727
    [No Abstract]   [Full Text] [Related]  

  • 3. Hair-nail dysplasia--a new pure autosomal dominant ectodermal dysplasia.
    Pinheiro M; Freire-Maia N
    Clin Genet; 1992 Jun; 41(6):296-8. PubMed ID: 1623625
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel connexin 30 mutation in Clouston syndrome.
    Smith FJ; Morley SM; McLean WH
    J Invest Dermatol; 2002 Mar; 118(3):530-2. PubMed ID: 11874494
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel mutations in GJB6 and GJB2 in Clouston syndrome.
    Liu YT; Guo K; Li J; Liu Y; Zeng WH; Geng SM
    Clin Exp Dermatol; 2015 Oct; 40(7):770-3. PubMed ID: 25808784
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction.
    Humbatova A; Maroofian R; Romano MT; Tafazzoli A; Behnam M; Dilaver N; Nouri N; Salehi M; Wolf S; Frank J; Kokordelis P; Betz RC
    Br J Dermatol; 2018 Apr; 178(4):e265-e267. PubMed ID: 29278420
    [No Abstract]   [Full Text] [Related]  

  • 7. Compound heterozygosity for novel KRT85 variants associated with pure hair and nail ectodermal dysplasia.
    Amico S; Ged C; Taïeb A; Morice-Picard F
    J Eur Acad Dermatol Venereol; 2019 Dec; 33(12):e458-e459. PubMed ID: 31273852
    [No Abstract]   [Full Text] [Related]  

  • 8. Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.
    Naeem M; John P; Ali G; Ahmad W
    Clin Exp Dermatol; 2007 Sep; 32(5):502-5. PubMed ID: 17489990
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.
    Celebi JT; Tanzi EL; Yao YJ; Michael EJ; Peacocke M
    J Invest Dermatol; 1999 Nov; 113(5):848-50. PubMed ID: 10571744
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity.
    Oh SW; Kim MY; Lee JS; Kim SC
    J Dermatol; 2006 Mar; 33(3):161-4. PubMed ID: 16620218
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clouston syndrome can mimic pachyonychia congenita.
    van Steensel MA; Jonkman MF; van Geel M; Steijlen PM; McLean WH; Smith FJ
    J Invest Dermatol; 2003 Nov; 121(5):1035-8. PubMed ID: 14708603
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of
    Agarwal N; Singh PK; Gupta K; Gupta N; Kabra M
    Indian J Dermatol Venereol Leprol; 2016; 82(6):697-700. PubMed ID: 27643550
    [No Abstract]   [Full Text] [Related]  

  • 13. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia.
    Fadhil M; Ghabra TA; Deeb M; Der Kaloustian VM
    Am J Med Genet; 1983 Feb; 14(2):335-46. PubMed ID: 6837628
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pachyonychia congenita and steatocystoma multiplex.
    Hodes ME; Norins AL
    Clin Genet; 1977 May; 11(5):359-64. PubMed ID: 577197
    [No Abstract]   [Full Text] [Related]  

  • 15. Family with autosomal dominant hidrotic ectodermal dysplasia: a previously unrecognised syndrome?
    Christianson AL; Fourie S
    Am J Med Genet; 1996 Jun; 63(4):549-53. PubMed ID: 8826433
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clouston syndrome and eccrine syringofibroadenomas.
    Poonawalla T; Xia L; Patten S; Stratman EJ
    Am J Dermatopathol; 2009 Apr; 31(2):157-61. PubMed ID: 19318801
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Nail diseases as a symptom of ectodermal dysplasia and related syndromes].
    Wollina U; Schaarschmidt H; Roth H
    Hautarzt; 1993 Aug; 44(8):503-11. PubMed ID: 8376103
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis.
    Baris HN; Zlotogorski A; Peretz-Amit G; Doviner V; Shohat M; Reznik-Wolf H; Pras E
    Br J Dermatol; 2008 Dec; 159(6):1373-6. PubMed ID: 18717672
    [No Abstract]   [Full Text] [Related]  

  • 19. Heritable nail diseases.
    Gass SF; Guberman RM; D'Orazi ST; Furci TJ
    Clin Podiatr Med Surg; 1989 Apr; 6(2):339-45. PubMed ID: 2650844
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pachyonychia congenita with candidiasis.
    Mawhinney H; Creswell S; Beare JM
    Clin Exp Dermatol; 1981 Mar; 6(2):145-9. PubMed ID: 7261468
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.