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Showing articles 0 to 9 of 9 Filter Applied: failure to thrive (Click to remove) FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 2000 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996 Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ Ann Neurol 34:25-31, Koo,B.,et al, 1993 MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991 Showing articles 0 to 9 of 9