Alpers syndrome with prominent white matter changes-Reference-Cited by-同舟云学术

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Alpers syndrome with prominent white matter changes

Published:2008-04 Issue:4 Volume:30 Page:295-300
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Bao Xinhua,Wu Ye,Wong Lee-Jun C.,Zhang Yuehua,Xiong Hui,Chou Ping-Chieh,Truong Cavatina K.,Jiang Yuwu,Qin Jiong,Yuan Yun,Lin Qing,Wu Xiru

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference27 articles.

1. Progressive neuronal degeneration of childhood with liver disease (Alpers–Huttenlocher syndrome): a personal review;Harding;J Child Neurol,1990

2. Infantile diffuse cerebral degeneration with hepatic cirrhosis;Huttenlocher;Arch Neurol,1976

3. Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers’ syndrome;Naviaux;Ann Neurol,1999

4. Mutations of mitochondrial DNA-polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia;Lamantea;Ann Neurol,2002

5. Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA;Ferrari;Brain,2005

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