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.
254 related articles for article (PubMed ID: 11568761)
21. 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]
22. Familial erythromelanosis follicularis faciei et colli with extensive keratosis pilaris. Lalit G; Anubhav G; Kumar KA; Asit M Int J Dermatol; 2011 Nov; 50(11):1400-1401. PubMed ID: 22004497 [No Abstract] [Full Text] [Related]
23. Monilethrix. Comparative scanning electron microscopic study of the hair in one family. Lubach D; Glowienka F; Castellucci M Dermatologica; 1982 Jan; 164(1):1-9. PubMed ID: 7067874 [TBL] [Abstract][Full Text] [Related]
24. The association of keratosis pilaris atrophicans with hereditary woolly hair. McHenry PM; Nevin NC; Bingham EA Pediatr Dermatol; 1990 Sep; 7(3):202-4. PubMed ID: 2247389 [No Abstract] [Full Text] [Related]
25. Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance. Celep F; Uzumcu A; Sonmez FM; Uyguner O; Balci YI; Bahadir S; Karaguzel A Genet Couns; 2009; 20(1):1-8. PubMed ID: 19400537 [TBL] [Abstract][Full Text] [Related]
26. [Hereditary skin diseases related to sex]. Desmons F; Walbaum R Lille Med; 1972 Mar; 17(3):447-70. PubMed ID: 4340312 [No Abstract] [Full Text] [Related]
31. Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization). Vega Gutiérrez J; Miranda-Romero A; Pérez Milán F; Martínez García G J Eur Acad Dermatol Venereol; 2004 Jul; 18(4):463-6. PubMed ID: 15196163 [TBL] [Abstract][Full Text] [Related]
32. [Keratosis pilaris and keratosis pilaris atrophicans faciei]. Arnold AW; Buechner SA J Dtsch Dermatol Ges; 2006 Apr; 4(4):319-23. PubMed ID: 16638061 [TBL] [Abstract][Full Text] [Related]
33. Multiple warty dyskeratomas on the scalp. Koç M; Kavala M; Kocatürk E; Mete O; Can B; Zindanci I; Aktas S Dermatol Online J; 2009 Feb; 15(2):8. PubMed ID: 19336025 [TBL] [Abstract][Full Text] [Related]
35. A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1. Winter H; Labrèze C; Chapalain V; Surlève-Bazeille JE; Mercier M; Rogers MA; Taieb A; Schweizer J J Invest Dermatol; 1998 Jul; 111(1):169-72. PubMed ID: 9665406 [TBL] [Abstract][Full Text] [Related]
36. Identification of two novel mutations in the Shen S; Shao M; Keyal U; Wang X; Li M; Zhang G Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33786625 [TBL] [Abstract][Full Text] [Related]
37. Olmsted syndrome: a case report and review of literature. Tao J; Huang CZ; Yu NW; Wu Y; Liu YQ; Li Y; Tian J; Yang LY; Zhang J; Li JW; Zhou YW; Tu YT Int J Dermatol; 2008 May; 47(5):432-7. PubMed ID: 18412857 [TBL] [Abstract][Full Text] [Related]