Results 131 to 140 of about 880 (178)
Melanin Biopolymers in Pharmacology and Medicine-Skin Pigmentation Disorders, Implications for Drug Action, Adverse Effects and Therapy. [PDF]
Karkoszka M, Rok J, Wrześniok D.
europepmc +1 more source
Progressive intertriginous plaques in a patient with fatigue and diarrhea. [PDF]
Momin B, Martini A, Fike J.
europepmc +1 more source
Waardenburg Syndrome in a Family.
Niveditha M, Prathap P, Asokan N.
europepmc +1 more source
Alezzandrini syndrome mimicking shingles - A rare case report with review of literature.
Singh M +5 more
europepmc +1 more source
Human piebaldism: six novel mutations of the proto-oncogene KIT
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
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
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
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
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

