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Showing articles 0 to 8 of 8 Filter Applied: short stature (Click to remove) A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 MELAS Syndrome Involving a Mother & Two Children Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987 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 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984 Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters Am J Med 69:64-74, Whythe,M.P.,et al, 1980 Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification Neurol 29:1057-1061, Markesbery,Wm.R., 1979 Showing articles 0 to 8 of 8