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Showing articles 0 to 13 of 13 Filter Applied: short stature (Click to remove) Dopamine-Responsive Dystonia eMedicine (Apr), Nikhar,N.K., 2006 Clinicopath Conf., MELAS Syndrome NEJM 353:2271-2280, Case 36-2005, 2005 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 Neurological Manifestations in Xeroderma Pigmentosum Ann Neurol 20:70-75, Mimaki,T.,et al, 1986 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 Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease (Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983 Child Abuse as a Cause of Post-Traumatic Hypopituitarism NEJM 302:724-728, Miller,W.L.,et al, 1980 Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification Neurol 29:1057-1061, Markesbery,Wm.R., 1979 A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings Ann Neurol 3:93, Fariello,R.,et al, 1978 Germinoma of third Ventricle (Case Record of MGH) NEJM 293:653, Locke,S.,et al, 1975 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 13 of 13