Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
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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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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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Heterogeneity of Coenzyme Q10 Deficiency
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Mitochondrial Therapy for Parkinson Disease
Arch Neurol 59:1523, Rosenberg,R.N., 2002
A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Acute Leukoencephalopathies:Differential Diagnosis and Investigation
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Generalized Mitochondrial Dysfunction in Parkinson's Disease Detected by Magnetic Resonance Spectroscopy of Muscle
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994
Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba
Neurol 44:843-845, Hirano,M.,et al, 1994
Mitochondrial Involvement in Parkinson's Disease:The Controversy Continues
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The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992
Mitochondrial Oxidative Phosphorylation Defects in Parkinson's Disease
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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