Acute Leukoencephalopathies:Differential Diagnosis and Investigation
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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
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018
Pyruvate Dehydrogenase Deficiency (PDCD)
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
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Cerebral MR Imaging in Uninfected Children Born to HIV-Seropositive Mothers and Perinatally Exposed to Zidovudine
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Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
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Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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