Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002
Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995
Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
AJNR 41:167-173, Bhatia,K.D.,et al, 2020
Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016
Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
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Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
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Metabolic Disease and Stroke: MELAS
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Mitochondrial Disease and Stroke
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Adult-Onset MELAS Presenting as Herpes Encephalitis
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Acute Leukoencephalopathies:Differential Diagnosis and Investigation
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Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
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Parkinson's Disease
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Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis
JNNP 65:233-240, Sue,C.M.,et al, 1998
Recurrent Strokes in a 34-Year-Old Man
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Adult-Onset MELAS
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Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
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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
Ann Neurol 34:25-31, Koo,B.,et al, 1993
Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993
MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988
Progressive Dystonia with Bilateral Putaminal Hypodensities
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MELAS Syndrome Involving a Mother & Two Children
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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