Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995
Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
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A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Cockayne Syndrome: Review of 140 Cases
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MELAS Syndrome Involving a Mother & Two Children
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Growth Hormone Treatment for Childhood Short Stature and Risk of Stroke in Early Adulthood
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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
Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985
Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
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Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979
Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978
Kearns-Sayre Syndrome & Hypoparathyroidism
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