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Publications by Xunhua Li
Overlapping Leigh Syndrome/Myoclonic Epilepsy With Ragged Red Fibres in an Adolescent Patient With a Mitochondrial DNA A8344G Mutation
Frontiers in Neurology
Neurology
Related publications
Clinical and Brain MR Imaging Features Focusing on the Brain Stem and Cerebellum in Patients With Myoclonic Epilepsy With Ragged-Red Fibers Due to Mitochondrial A8344G Mutation
American Journal of Neuroradiology
Medicine
Nuclear Medicine
Neurology
Imaging
Radiology
Phenotypic Diversity of Myoclonus Epilepsy Associated With Ragged-Red Fibers With an 8344A>G mtDNA Mutation
Internal Medicine
Internal Medicine
Medicine
Mitochondrial DNA-associated Leigh Syndrome
Wolff-Parkinson-White Syndrome in a Patient With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Mimicking Juvenile Myoclonic Epilepsy
Journal of Clinical Neurology (Korea
Neurology
Senile Myoclonic Epilepsy in Down Syndrome With Dementia
Journal of the Turkish Epilepsi Society
Falling After Starting Running in a Case of Myoclonus Epilepsy Associated With Ragged-Red Fibers With a 8344A>G mtDNA Mutation
Internal Medicine
Internal Medicine
Medicine
Defective Kinetics of Cytochrome C Oxidase and Alteration of Mitochondrial Membrane Potential in Fibroblasts and Cytoplasmic Hybrid Cells With the Mutation for Myoclonus Epilepsy With Ragged-Red Fibres (‘MERRF’) at Position 8344 Nt
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
UBR5Gene Mutation Is Associated With Familial Adult Myoclonic Epilepsy in a Japanese Family
ISRN Neurology
A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
