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Showing articles 0 to 11 of 11 Filter Applied: failure to thrive (Click to remove) Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss Neurol 90:e625-e631, Set, K.K.,et al, 2018 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 Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 A Floppy Child with Failure to Thrive Lancet 366:176, Loma-Sanner,I.,et al, 2005 Physical Features of Prader-Willi Syndrome in Neonates Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990 Clinicopath. Conference Acquired Immunodeficiency Syndrome, Rhabdomyosarcoma, with Extensive Metastases, Case 9-1986, NEJM 3, 4:620,1986., 1986 Alexander's Disease, A Disease of Astrocytes Brain 108:367-385, Borrett,D.&Becker,L.E., 1985 The Cornelia de Lange Syndrome J Pediatr 63:1000-1020, Ptacek,L.J., 1963 Showing articles 0 to 11 of 11