230 related articles for article (PubMed ID: 12942186)
1. [Genetically induced hair diseases].
Wiederholt T; Poblete-Gutiérrez P; Frank J
Hautarzt; 2003 Aug; 54(8):723-31. PubMed ID: 12942186
[TBL] [Abstract][Full Text] [Related]
2. Unveiling the roots of monogenic genodermatoses: genotrichoses as a paradigm.
Betz RC; Cabral RM; Christiano AM; Sprecher E
J Invest Dermatol; 2012 Mar; 132(3 Pt 2):906-14. PubMed ID: 22170492
[TBL] [Abstract][Full Text] [Related]
3. Unraveling the molecular mechanisms of hair and nail genodermatoses.
Stratigos AJ; Baden HP
Arch Dermatol; 2001 Nov; 137(11):1465-71. PubMed ID: 11708949
[TBL] [Abstract][Full Text] [Related]
4. [Hair anomalies in syndromic disorders].
Frank J; Betz RC
Hautarzt; 2019 Jul; 70(7):514-519. PubMed ID: 31197391
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetics of alopecias.
Ramot Y; Zlotogorski A
Curr Probl Dermatol; 2015; 47():87-96. PubMed ID: 26370647
[TBL] [Abstract][Full Text] [Related]
6. Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: an update.
Nakamura M; Schneider MR; Schmidt-Ullrich R; Paus R
J Dermatol Sci; 2013 Jan; 69(1):6-29. PubMed ID: 23165165
[TBL] [Abstract][Full Text] [Related]
7. A review of genotrichoses and hair pathology associated with inherited skin diseases.
Doolan BJ; Rayinda T; Chiu FP; McGrath JA; Onoufriadis A
Br J Dermatol; 2023 Jul; 189(2):154-160. PubMed ID: 36978220
[TBL] [Abstract][Full Text] [Related]
8. Alopecia in genetic diseases.
Calvieri S; Rossi A
G Ital Dermatol Venereol; 2014 Feb; 149(1):1-13. PubMed ID: 24566562
[TBL] [Abstract][Full Text] [Related]
9. [Genetic hair diseases. An update].
Frank J; Poblete-Gutiérrez P; Giehl K
Hautarzt; 2013 Nov; 64(11):830-42. PubMed ID: 24177665
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.
Khan S; Habib R; Mir H; Umm-e-Kalsoom ; Naz G; Ayub M; Shafique S; Yamin T; Ali N; Basit S; Wasif N; Kamran-Ul-Hassan Naqvi S; Ali G; Wali A; Ansar M; Ahmad W
Clin Exp Dermatol; 2011 Aug; 36(6):652-4. PubMed ID: 21426374
[TBL] [Abstract][Full Text] [Related]
11. Clinical trichology.
Bartosová L; St'áva Z; Jorda V
Curr Probl Dermatol; 1984; 12():59-184. PubMed ID: 6238807
[No Abstract] [Full Text] [Related]
12. Heritable disorders of hair.
Birnbaum PS; Baden HP
Dermatol Clin; 1987 Jan; 5(1):137-53. PubMed ID: 3549074
[TBL] [Abstract][Full Text] [Related]
13. The genetics of hair shaft disorders.
Cheng AS; Bayliss SJ
J Am Acad Dermatol; 2008 Jul; 59(1):1-22; quiz 23-6. PubMed ID: 18571596
[TBL] [Abstract][Full Text] [Related]
14. To grow or not to grow: hair morphogenesis and human genetic hair disorders.
Duverger O; Morasso MI
Semin Cell Dev Biol; 2014; 25-26():22-33. PubMed ID: 24361867
[TBL] [Abstract][Full Text] [Related]
15. Molecular basis of congenital atrichia in humans and mice.
Ahmad W; Panteleyev A; Christiano AM
Cutis; 1999 Oct; 64(4):269-76. PubMed ID: 10544884
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis.
Shimomura Y; Sakamoto F; Kariya N; Matsunaga K; Ito M
J Invest Dermatol; 2006 Jun; 126(6):1281-5. PubMed ID: 16439973
[TBL] [Abstract][Full Text] [Related]
17. [A syndrome: uncombable hair. Observation of 6 members of a family with pili canaliculi, associated with pili torti, progressive alopecia, atopic eczema and hamartomas].
Braun-Falco O; Ryckmanns F; Heilgemeir GP; Ring J
Hautarzt; 1982 Jul; 33(7):366-72. PubMed ID: 7107281
[TBL] [Abstract][Full Text] [Related]
18. Genetic hair and nail disorders.
Sprecher E
Clin Dermatol; 2005; 23(1):47-55. PubMed ID: 15708289
[TBL] [Abstract][Full Text] [Related]
19. A novel mutation, c.699C>G (p.C233W), in the LIPH gene leads to a loss of the hydrolytic activity and the LPA6 activation ability of PA-PLA1α in autosomal recessive wooly hair/hypotrichosis.
Yoshizawa M; Nakamura M; Farooq M; Inoue A; Aoki J; Shimomura Y
J Dermatol Sci; 2013 Oct; 72(1):61-4. PubMed ID: 23768866
[No Abstract] [Full Text] [Related]
20. [Loose anagen hair syndrome: a familial case with fetal hair in meconium].
Khadir K; Habibeddine S; Azzouzi S; Lakhdar H; Van Neste D
Ann Dermatol Venereol; 2001 Jan; 128(1):52-4. PubMed ID: 11226903
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
