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Keyword [MELAS]
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1. Study Of Mitochondrial DNA Point Mutation In Patients With Basal Ganglia Calcification On Cranial CT
2. The Study Of Pathology And Gene Mutation In Patients With Mitochondrial Encephalomyopathies
3. The Studies On The Expression Of Anti-mitochondrial Antibody In The Brain And Muscle Fibers Of Patients With MELAS Syndrome
4. Association Between Heteroplasmy Level Of The Mitochondrial TRNALeu(UUR) A3243G Mutation And Clinical Features In A Chinese Family With Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-like Episodes Syndrome
5. A Clinical And Basic Research On Mitochondrial Encephalomyopathy, Lactic Acidosis And Stroke-like Episodes
6. Clinical Analysis Of25Cases With Metabolic Myopathies And Significance And Expression Of Anti-mitochondrial Antibody, Bcl-2and Bax
7. The Clinical, Radiographic And Pathological Analysis Of MELAS And Its Pathogenesis Resulted From NO Decrease
8. The Clinical, Pathological And Molecular Studies Of A Mitochondrial Encephalomyopathy Family
9. Clinical Features Of Mitochondrial Myopathy, Encephalopathy,Lactic Acidosis And Stroke-like Episodes Syndrome
10. The Clinical Features, Iconography, Pathologic And Gene Analysis Of MELAS And The Study Of The Relationship Between MELAS And Mitophagy
11. Clinical Study Of Mitochondrial Encephalomyopathies MELAS In Children
12. The Clinical And Genetic Analysis Of Heteroplasmic 3243A>G Mutation In Mitochondrial TRNALeu（UUR） Gene Among 6 Chinese Patients With MELAS
13. Study Of Aberrantly Expressed Non-coding RNAs Involved In The Pathogenesis Of Mitochondrial Myopathy And Potential Clinical Implications
14. Clinical Manifestation, Image, Electroencephalogram And Genetic Study In MELAS Syndrom
15. The Clinical,Imaging,Pathology And Genetic Analysis Of 24 Patients With MELAS Syndrome
16. The Combined Application Of Two Sets Of Diagnostic Criteria In 56 Patients With Suspected Mitochondrial Encephalomyopathy
17. Study Of Epilepsic Seizures And Electrophysiologic Characteristics In Patients With MELAS
18. Progress In Clinical,Imaging And Gene Mutation Of MELAS Syndrome
19. The Clinical Phenotype,Genotype And Mechanism Of Unbalanced Mitochondrial Homeostasis In Mitochondrial Encephalomyopathy
20. The Clinical Characteristics And Prognostic Factors Of Epilepsy Associated With Mitochondrial Encephalomyopathy,Lactic Acidosis,and Stroke-like Episodes(MELAS)
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