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.
116 related articles for article (PubMed ID: 14939114)
21. SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies. Mauri L; Barone L; Al Oum M; Del Longo A; Piozzi E; Manfredini E; Stanzial F; Benedicenti F; Penco S; Patrosso MC Gene; 2014 Jan; 533(1):398-402. PubMed ID: 24096233 [TBL] [Abstract][Full Text] [Related]
22. Poliosis circumscripta: overview and underlying causes. Sleiman R; Kurban M; Succaria F; Abbas O J Am Acad Dermatol; 2013 Oct; 69(4):625-33. PubMed ID: 23850259 [TBL] [Abstract][Full Text] [Related]
23. Biology and genetics of oculocutaneous albinism and vitiligo - common pigmentation disorders in southern Africa. Manga P; Kerr R; Ramsay M; Kromberg JG S Afr Med J; 2013 Jul; 103(12 Suppl 1):984-8. PubMed ID: 24300644 [TBL] [Abstract][Full Text] [Related]
24. [Partial familial albinism (piebaldism): ultrastructural study]. Grupper C; Pruniéras M; Hincky M; Garelly E Ann Dermatol Syphiligr (Paris); 1970; 97(3):267-86. PubMed ID: 5455226 [No Abstract] [Full Text] [Related]
25. ELECTRON MICROSCOPY OF MELANOCYTES IN HUMAN PIEBALDISM. BREATHNACH AS; FITZPATRICK TB; WYLLIE LM J Invest Dermatol; 1965 Jul; 45():28-37. PubMed ID: 14310308 [No Abstract] [Full Text] [Related]
26. Silvery hair with dyschromatosis: Griscelli syndrome type 3 or familial gigantic melanocytosis. Batrani M; Thole A; Kubba A; Mahajan K J Cutan Pathol; 2018 Dec; 45(12):918-922. PubMed ID: 30129079 [TBL] [Abstract][Full Text] [Related]
31. Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism. King RA; Townsend D; Oetting W; Summers CG; Olds DP; White JG; Spritz RA J Clin Invest; 1991 Mar; 87(3):1046-53. PubMed ID: 1900307 [TBL] [Abstract][Full Text] [Related]
32. Mutation analysis in a family with oculocutaneous albinism manifesting in the same generation of three branches. Preising MN; Forster H; Tan H; Lorenz B; de Jong PT; Plomp AS Mol Vis; 2007 Oct; 13():1851-5. PubMed ID: 17960121 [TBL] [Abstract][Full Text] [Related]
33. Repigmentation of White Forelock in a Familial Case of Piebaldism Reported via Teledermatology in the COVID-19 Era. Gaudiello F; Ferrillo M; Vastarella M; Fabbrocini G; Patrì A Skin Appendage Disord; 2021 Feb; 7(2):120-122. PubMed ID: 33791342 [TBL] [Abstract][Full Text] [Related]
34. Mice transgenic for Kit(V620A): recapitulation of piebaldism but not progressive depigmentation seen in humans with this mutation. Tosaki H; Kunisada T; Motohashi T; Aoki H; Yoshida H; Kitajima Y J Invest Dermatol; 2006 May; 126(5):1111-8. PubMed ID: 16456533 [TBL] [Abstract][Full Text] [Related]
35. Variable expression of vision in sibs with albinism. Summers CG; Creel D; Townsend D; King RA Am J Med Genet; 1991 Sep; 40(3):327-31. PubMed ID: 1951438 [TBL] [Abstract][Full Text] [Related]
36. Squamous-cell carcinoma in situ in a patient with oculocutaneous albinism. Berger E; Hunt R; Tzu J; Patel R; Sanchez M Dermatol Online J; 2011 Oct; 17(10):22. PubMed ID: 22031648 [TBL] [Abstract][Full Text] [Related]