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: 2591617)

  • 21. [Marie Unna hereditary hypotrichosis].
    Lalevíc-Vasić BM; Polić D; Nikolić MM
    Ann Dermatol Venereol; 1992; 119(1):25-9. PubMed ID: 1562148
    [No Abstract]   [Full Text] [Related]  

  • 22. Keratosis follicularis spinulosa decalvans in a family.
    Bellet JS; Kaplan AL; Selim MA; Olsen EA
    J Am Acad Dermatol; 2008 Mar; 58(3):499-502. PubMed ID: 18280351
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [On 3 generations of congenital keratosis follicularis with alopecia, hyperhidrosis and abortive palmar-plantar keratoses limited to women and its relation to congenital hereditary hypotrichosis].
    GREITHER A
    Arch Klin Exp Dermatol; 1960; 210():123-40. PubMed ID: 13851750
    [No Abstract]   [Full Text] [Related]  

  • 24. Pitfalls and pearls in the diagnosis of monilethrix.
    Leitner C; Cheung S; de Berker D
    Pediatr Dermatol; 2013; 30(5):633-5. PubMed ID: 23834295
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Analysis of hair from alopecia congenita.
    Baden HP; Kubilus J
    J Am Acad Dermatol; 1980 Dec; 3(6):623-6. PubMed ID: 7204679
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Two brothers with keratosis follicularis spinulosa decalvans.
    Alfadley A; Al Hawsawi K; Hainau B; Al Aboud K
    J Am Acad Dermatol; 2002 Nov; 47(5 Suppl):S275-8. PubMed ID: 12399750
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Follicular ichthyosis.
    Hazell M; Marks R
    Br J Dermatol; 1984 Jul; 111(1):101-9. PubMed ID: 6743535
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
    Düzenli S; Redler S; Müller M; Polat M; Dogruer D; Pasternack SM; Betz RC
    Clin Exp Dermatol; 2009 Dec; 34(8):e953-6. PubMed ID: 20055871
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Keratosis follicularis spinulosa decalvans. Report of two cases and literature review.
    Rand R; Baden HP
    Arch Dermatol; 1983 Jan; 119(1):22-6. PubMed ID: 6336927
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A case of alopecia universalis without the involvement of scalp hairs.
    Yoon KH; Lee SH; Ahn SK; Lee WS
    Yonsei Med J; 1995 Mar; 36(1):97-101. PubMed ID: 7740842
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical, dermoscopic, and histopathologic features of body hair disorders.
    Panchaprateep R; Tanus A; Tosti A
    J Am Acad Dermatol; 2015 May; 72(5):890-900. PubMed ID: 25748313
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Hereditary congenital hypotrichosis, Marie Unna type].
    Chlebarov S
    Z Hautkr; 1985 Apr; 60(7):583-96. PubMed ID: 4002769
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hair.
    Mehmood S; Jan A; Muhammad D; Ahmad F; Mir H; Younus M; Ali G; Ayub M; Ansar M; Ahmad W
    Australas J Dermatol; 2015 Aug; 56(3):e66-70. PubMed ID: 24628704
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Keratosis pilaris decalvans non-atrophicans.
    Drago F; Maietta G; Parodi A; Rebora A
    Clin Exp Dermatol; 1993 Jan; 18(1):45-6. PubMed ID: 8440051
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B; Hundeiker M
    Fortschr Med; 1979 Nov; 97(44):2018-22. PubMed ID: 511082
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Case for diagnosis].
    de Carvalho CV; Bastazini Junior I; Barreto JA; Duarte Ide B; de Figueiredo RB
    An Bras Dermatol; 2009; 84(5):539-41. PubMed ID: 20098861
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Graham-Little syndrome.
    Zegarska B; Kallas D; Schwartz RA; Czajkowski R; Uchanska G; Placek W
    Acta Dermatovenerol Alp Pannonica Adriat; 2010 Oct; 19(3):39-42. PubMed ID: 20976421
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hereditary hypotrichosis of the scalp.
    Hess RO; Uno H
    Am J Med Genet; 1991 May; 39(2):125-9. PubMed ID: 2063912
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hereditary hypotrichosis simplex of the scalp.
    Rodríguez Díaz E; Fernández Blasco G; Martín Pascual A; Armijo M
    Dermatology; 1995; 191(2):139-41. PubMed ID: 8520061
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.
    Shimomura Y; Garzon MC; Kristal L; Shapiro L; Christiano AM
    Exp Dermatol; 2009 Mar; 18(3):218-21. PubMed ID: 18803659
    [TBL] [Abstract][Full Text] [Related]  

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