Neuropathologic and clinical features in eight Chinese patiens with Leigh disease

Journal of Child Neurology

Volumn 17, Issue 6, 2002, Pages 450-452

  Jiang, Yu Wu ^a   Qin, Jiong ^a   Yuan, Yun ^a   Qi, Yu ^a   Wu, Xi Ru ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

AGE; ARTICLE; BASAL GANGLION; BRAIN DEGENERATION; BRAIN NECROSIS; BRAIN STEM; CAPILLARY PROLIFERATION; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; DNA DETERMINATION; FEMALE; GENE MUTATION; HUMAN; HUMAN TISSUE; INFANT; INHERITANCE; LEIGH DISEASE; MALE; NEUROLOGIC EXAMINATION; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; PUTAMEN; SYMPTOM;

EID: 0036592883     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380201700611     Document Type: Article

References (10)

1. Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications
2. Oral glucose lactate stimulation test in mitochondrial diseases
3. Neuroradiologic findings in children with mitochondrial disorders
4. Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency
5. Leigh syndrome in a 3-year-old boy with unusual brain MR imaging and pathologic findings
6. Phenotypic differences between T E C and T Æ G mutations at nt 8993 of mitochondrial DNA in Leigh syndrome
7. Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: A clinical, biochemical, and molecular study in six families