Results 131 to 140 of about 880 (178)

Waardenburg Syndrome in a Family.

open access: yesInt J Trichology
Niveditha M, Prathap P, Asokan N.
europepmc   +1 more source

Piebaldism

open access: yesJournal of Dermatology, 2013
Naoki Oiso, Tamio Suzuki
exaly   +3 more sources

Human piebaldism: six novel mutations of the proto-oncogene KIT

open access: yesHuman Mutation, 2002
Human piebaldism is a rare autosomal dominant disorder that comprises congenital patchy depigmentation of the scalp, forehead, trunk and limbs. It is caused by mutations in the cell-surface receptor tyrosine kinase gene (KIT, also c-kit).
Petros Syrris   +2 more
exaly   +2 more sources

Permanent repigmentation of piebaldism by erbium:YAG laser and autologous cultured epidermis

open access: yesBritish Journal of Dermatology, 2004
BACKGROUND: Several surgical techniques have been proposed for the treatment of piebaldism. These procedures, however, are poorly suited for the treatment of large leucodermal lesions, can cause scars and require multiple donor sites.
Liliana Guerra   +2 more
exaly   +2 more sources

Deletion of the SLUG (SNAI2) gene results in human piebaldism

open access: yesAmerican Journal of Medical Genetics, Part A, 2003
Slug is a zinc-finger neural crest transcription factor, encoded by the SLUG gene, which is critical for development of hematopoietic stem cells, germ cells, and melanoblasts in the mouse.
Manuel Sánchez-Martín   +2 more
exaly   +2 more sources

Optimising size and depth of punch grafts in autologous transplantation of vitiligo and piebaldism: a randomised controlled trial

open access: yesJournal of Dermatological Treatment, 2017
Background: To date, autologous punch grafting appears to be the easiest and least expensive surgical technique for stable vitiligo and piebaldism. Punch grafting is available worldwide, with no need for specialised instruments. However, no reliable data
C A C Prinsen   +2 more
exaly   +2 more sources

Analysis of KIT, SCF, and Initial Screening of SLUG in Patients with Piebaldism

open access: yesJournal of Investigative Dermatology, 2005
Piebaldism is an autosomal dominant disorder, characterized by congenital leukoderma typically on the abdomen, knees, and forehead. Mice models for human piebaldism are the W dominant white spotting, the steel mice and the mice that are mutated for the ...
Naoki Oiso   +2 more
exaly   +2 more sources

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