Skin manifestations of a patient with mitochondrial encephalomyopathy with lactic acidosis and strokelike episodes (MELAS syndrome)-Reference-Cited by-同舟云学术

Skin manifestations of a patient with mitochondrial encephalomyopathy with lactic acidosis and strokelike episodes (MELAS syndrome)

Published:1999-09 Issue:3 Volume:41 Page:469-473
ISSN:0190-9622
Container-title:Journal of the American Academy of Dermatology
language:en
Short-container-title:Journal of the American Academy of Dermatology

Author:

Kubota Yasuo,Ishii Toshiya,Sugihara Hiroshi,Goto Yu-ichi,Mizoguchi Masako

Publisher

Elsevier BV

Subject

Dermatology

Reference8 articles.

1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome associated with ragged-red fibers;Pavlakis;Ann Neurol,1984

2. MELAS syndrome involving mother and two children;Driscoll;Arch Neurol,1987

3. A mutation in the tRNA Leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies;Goto;Nature,1990

4. A case of mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS) with hypertrichosis;Hashimoto;Jpn J Clin Dermatol (Rinsho Hifuka),1998

5. Two siblings with mitochondrial encephalomyopathy associated with myoglobinuria and ichthyosis [abstract];Kinui;Clin Neurol,1989

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