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Items: 1 to 20 of 87

1.

Piebaldism: A brief report and review of the literature.

Agarwal S, Ojha A.

Indian Dermatol Online J. 2012 May;3(2):144-7. doi: 10.4103/2229-5178.96722.

2.

Piebaldism.

Hazan C.

Dermatol Online J. 2005 Dec 30;11(4):18.

3.

Piebaldism in a 2-year-old girl.

López V, Jordá E.

Dermatol Online J. 2011 Feb 15;17(2):13. Review.

4.

A novel mutation of the KIT gene in a Chinese family with piebaldism.

Wen GD, Zhou C, Yu C, DU J, Xu QX, Liu ZY, Zhang JZ.

Chin Med J (Engl). 2013 Jun;126(12):2325-8.

5.

A piebald family.

Gupta LK, Maru S, Mittal A, Masuria BL, Sharma M, Bansal NK.

Indian J Dermatol Venereol Leprol. 1996 Jul-Aug;62(4):233-4.

6.

[Piebaldism: a pigmentary anomaly to recognize: about a case and review of the literature].

El Kouarty H, Dakhama BS.

Pan Afr Med J. 2016 Nov 14;25:155. doi: 10.11604/pamj.2016.25.155.10499. eCollection 2016 Nov 14. French.

7.

[Piebaldism].

Küster W.

Hautarzt. 1987 Aug;38(8):481-3. German.

PMID:
3654219
8.

A novel KIT mutation results in piebaldism with progressive depigmentation.

Richards KA, Fukai K, Oiso N, Paller AS.

J Am Acad Dermatol. 2001 Feb;44(2):288-92.

PMID:
11174389
9.

Piebaldism: an autonomous autosomal dominant entity.

Winship I, Young K, Martell R, Ramesar R, Curtis D, Beighton P.

Clin Genet. 1991 May;39(5):330-7.

PMID:
1860249
10.

Piebaldism in a 3-month-old infant--case report.

Milankov O, Savić R, Radulović A.

Med Pregl. 2014 Mar-Apr;67(3-4):109-10.

PMID:
24961053
11.

Café-au-lait macules and intertriginous freckling in piebaldism: clinical overlap with neurofibromatosis type 1 and Legius syndrome.

Stevens CA, Chiang PW, Messiaen LM.

Am J Med Genet A. 2012 May;158A(5):1195-9. doi: 10.1002/ajmg.a.35297. Epub 2012 Mar 21.

PMID:
22438235
12.

The molecular genetics of albinism and piebaldism.

Tomita Y.

Arch Dermatol. 1994 Mar;130(3):355-8. Review.

PMID:
8129415
13.

A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling.

Jia WX, Xiao XM, Wu JB, Ma YP, Ge YP, Li Q, Mao QX, Li CR.

Ther Clin Risk Manag. 2015 Apr 21;11:635-8. doi: 10.2147/TCRM.S75544. eCollection 2015 Apr 21.

14.

Piebaldism: a case report and a concise review of the literature.

Janjua SA, Khachemoune A, Guldbakke KK.

Cutis. 2007 Nov;80(5):411-4. Review.

PMID:
18189028
15.

Human piebaldism: relationship between phenotype and site of kit gene mutation.

Ward KA, Moss C, Sanders DS.

Br J Dermatol. 1995 Jun;132(6):929-35.

PMID:
7544995
16.

Spontaneous contraction of leukodermic patches in Waardenburg syndrome.

Chang T, Hashimoto K, Bawle EV.

J Dermatol. 1993 Nov;20(11):707-11.

PMID:
8300941
17.

Association of piebaldism and neurofibromatosis type 1 in a girl.

Angelo C, Cianchini G, Grosso MG, Zambruno G, Cavalieri R, Paradisi M.

Pediatr Dermatol. 2001 Nov-Dec;18(6):490-3.

PMID:
11841634
18.

Piebaldism in children.

Grob A, Grekin S.

Cutis. 2016 Feb;97(2):90-2. Review.

PMID:
26919497
19.

Ultrastructural study of two patients with both piebaldism and neurofibromatosis 1.

Chang T, McGrae JD Jr, Hashimoto K.

Pediatr Dermatol. 1993 Sep;10(3):224-34; discussion 288.

PMID:
8415298
20.

Piebaldism--a case report.

Hwang SM, Ahn SK, Lee WS, Yoo MS, Choi EH.

J Korean Med Sci. 1996 Jun;11(3):285-8.

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