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Showing articles 0 to 8 of 8 Filter Applied: hypotonia,infants (Click to remove) Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980 Congenital Cytomegalovirus Infection BMJ 373:m1212, Pesch, M.H.,et al, 2021 Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease) Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996 Congenital Inflammatory Myopathy Neurol 40:1111-1114, Shevell,M.,et al, 1990 Rett Syndrome:Natural History and Management Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988 Guillain-Barre Syndrome with Hydrocephalus in Early Infancy Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977 Showing articles 0 to 8 of 8