Leigh Disease:Value of CT in Presymptomatic Patients and Variability of the Lesions with Time
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Mitochondrial DNA and Genetic Disease
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Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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A Defect in Mitochondrial Electron-Transport Activity in Leber's Hereditary Optic Neuropathy
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Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
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Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases
J Comput Assist Tomogr 12:40-44, Geyer,C.A.,et al, 1988
MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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Diagnosis & Follow-up of Mitochondrial Encephalomyopathy:CT and MR Studies
J Comput Assist Tomogr 12:696-697, Taverni,N.,et al, 1988
Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988
Significance of Basal Ganglia Calcification on Computed Tomography in Children
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Progressive Dystonia with Bilateral Putaminal Hypodensities
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MELAS Syndrome Involving a Mother & Two Children
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Magnetic Resonance Imaging in Autopsy-Proved Adult Subacute Necrotizing Encephalomyelopathy (Leigh's Disease)
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Abnormalities of Eyelid Closure
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
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Ophthalmoscopy of the Retinal Nerve Fiber Layer
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Ophthalmoplegia-Plus
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Demyelinating Radiculopathy in the Kearns-Sayre Syndrome:A Clinicopathological Study
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Specificity of the Urine Inhibitor Test for Leigh's Disease
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Encephalomyelopathy of Leigh
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Chronic Progressive External Ophthalmoplegia
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Subacute Necrotizing Encephalopathy in Late Adolescence
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