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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Pediatric Leigh Syndrome
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Cerebral MR Imaging in Uninfected Children Born to HIV-Seropositive Mothers and Perinatally Exposed to Zidovudine
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Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,et al, 2018
Rapidly Progressive Leukoencephalopathy in Mitochondrial Complex I Deficiency
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Clinico-Radiological Spectrum of Bilateral Temporal Lobe Hyperintensity: A Retrospective Review
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
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Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia
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Metabolic Disease and Stroke: MELAS
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Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
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Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004
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
Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
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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 Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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