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Mitochondrial DNA and Disease
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Cockayne Syndrome: Review of 140 Cases
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
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A 40-Year-Old Woman Presenting with Distal Leg Weakness
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke
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Clinicopath Conf., MELAS Syndrome
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Mitochondrial Respiratory-Chain Diseases
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Prader-Willi and Angelman Syndromes
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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A Clinical Study of Noonan Syndrome
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Craniopharyngyoma in Children
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MELAS Syndrome Involving a Mother & Two Children
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Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
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Paraparesis in Hereditary Multiple Exostoses:Case Report
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Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
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Kearns-Sayre Syndrome & Hypoparathyroidism
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