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Recurrent Strokes in a 34-Year-Old Man
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Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009
Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002
A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Mitochondrial Disease and Stroke
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Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
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Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995
Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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MELAS Syndrome Involving a Mother & Two Children
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