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Showing articles 0 to 13 of 13 Filter Applied: hypotonia (Click to remove) Huntington Disease: Clinical Features and Diagnosis UptoDate Dec 2017, Oksana Suchowersky, 2017 The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder Brain 133:655-670, Leen,W.G., et al, 2010 Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up AJNR 30:1971-1976, Uggetti,C.,et al, 2009 The Floppy Infant: Evaluation of Hypotonia Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 An Infant with Encephalitis Lancet 350:1594, Yeung,W.L.,et al, 1997 Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996 Postoperative Neurologic Complications after Open Heart Surgery on Young Infants Arch Pediatr Adolesc Med 149:764-768, Miller,G.,et al, 1995 Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis Medicine 70:99-117, Gatti,R.A.,et al, 1991 Physical Features of Prader-Willi Syndrome in Neonates Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990 Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger Ann Neurol 2:473, deLeon,G.A.,et al, 1977 Showing articles 0 to 13 of 13