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Showing articles 0 to 12 of 12 Filter Applied: short stature (Click to remove) Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder Neurol 44:721-727, Hirano,M.,et al, 1994 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Kearns-Sayre Syndrome & Hypoparathyroidism Ann Neurol 3:455, Pellock,J.M.,et al, 1978 Kearns-Sayre Syndrome with Hypoparathyroidism Ann Neurol 3:513, Horwitz,S.J.,et al, 1978 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992 Clinicopathological Conference Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983 Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease (Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983 A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings Ann Neurol 3:93, Fariello,R.,et al, 1978 Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue (Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972 Showing articles 0 to 12 of 12