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 *

161 related articles for article (PubMed ID: 139851)

  • 1. Hidrotic ectodermal dysplasia: study of a large Chinese pedigree.
    Rajagopalan K; Tay CH
    Arch Dermatol; 1977 Apr; 113(4):481-5. PubMed ID: 139851
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hidrotic form of ectodermal dysplasia].
    Bolck F; Barth C
    Z Hautkr; 1973 Dec; 48(24):1041-8. PubMed ID: 4273177
    [No Abstract]   [Full Text] [Related]  

  • 3. Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma.
    Dinani N; Ali M; Liu L; McGrath J; Mellerio J
    Clin Exp Dermatol; 2017 Apr; 42(3):316-319. PubMed ID: 28239884
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hidrotic ectodermal dysplasia in a black mother and daughter.
    McNaughton PZ; Pierson DL; Rodman OG
    Arch Dermatol; 1976 Oct; 112(10):1448-50. PubMed ID: 962343
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clouston syndrome: a rare autosomal dominant trait with palmoplantar hyperkeratosis and alopecia.
    Patel RR; Bixler D; Norins AL
    J Craniofac Genet Dev Biol; 1991; 11(3):176-9. PubMed ID: 1837030
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A family with palmoplantar epidermolytic hyperkeratosis.
    Berth-Jones J; Hutchinson PE
    Clin Exp Dermatol; 1989 Jul; 14(4):313-6. PubMed ID: 2531643
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait.
    Tolmie JL; Wilcox DE; McWilliam R; Assindi A; Stephenson JB
    J Med Genet; 1988 Nov; 25(11):754-7. PubMed ID: 2976839
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A patient with alopecia, nail dystrophy, palmoplantar hyperkeratosis, keratitis, hearing difficulty and micrognathia without GJB2 or GJB6 mutations: a new type of hidrotic ectodermal dysplasia?
    Nakamura M; Ishikawa O
    Br J Dermatol; 2007 Apr; 156(4):777-9. PubMed ID: 17298485
    [No Abstract]   [Full Text] [Related]  

  • 9. Diffuse Palmoplantar Keratoderma, Onychodystrophy, universal Hypotrichosis and Cysts.
    Arif T; Amin SS; Adil M; Mohtashim M
    Acta Dermatovenerol Croat; 2017 Jul; 25(2):161-163. PubMed ID: 28871934
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hidrotic ectodermal dysplasia].
    Altmeyer P; Schindera I
    Hautarzt; 1975 Dec; 26(12):631-7. PubMed ID: 1213883
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation.
    Akasaka E; Nakano H; Nakano A; Toyomaki Y; Takiyoshi N; Rokunohe D; Nishikawa Y; Korekawa A; Matsuzaki Y; Mitsuhashi Y; Sawamura D
    Br J Dermatol; 2011 Dec; 165(6):1290-2. PubMed ID: 21801157
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family.
    Aswegan AL; Josephson KD; Mowbray R; Pauli RM; Spritz RA; Williams MS
    Am J Med Genet; 1997 Nov; 72(4):462-7. PubMed ID: 9375732
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of a known GJB6 mutation in an autosomal dominant inherited Chinese family with hidrotic ectodermal dysplasia.
    Mousumi T; Xiong Z; Lu L; Liu S; Xia K; Hu Z
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2013 Aug; 38(8):761-5. PubMed ID: 23981984
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia.
    Calzavara-Pinton P; Carlino A; Benetti A; De Panfilis G
    Dermatologica; 1991; 182(3):184-7. PubMed ID: 1879585
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations.
    Kantaputra P; Kaewgahya M; Jotikasthira D; Kantaputra W
    Am J Med Genet A; 2014 Apr; 164A(4):1041-8. PubMed ID: 24458874
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ectodermal dysplasia-skin fragility syndrome: Two new cases and review of this desmosomal genodermatosis.
    Doolan BJ; Gomaa NS; Fawzy MM; Dogheim NN; Liu L; Mellerio JE; Onoufriadis A; McGrath JA
    Exp Dermatol; 2020 Jun; 29(6):520-530. PubMed ID: 32248567
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2.
    Naeem M; Jelani M; Lee K; Ali G; Chishti MS; Wali A; Gul A; John P; Hassan MJ; Leal SM; Ahmad W
    Br J Dermatol; 2006 Dec; 155(6):1184-90. PubMed ID: 17107387
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N; Jordaan FH; Taljaard JJ; Hough SF
    Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.