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Showing articles 0 to 8 of 8 Filter Applied: hypotonia,infants (Click to remove) Guillain-Barre Syndrome with Hydrocephalus in Early Infancy Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977 A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes Neurol 102:e209258, Lail,G.,et al, 2024 Congenital Cytomegalovirus Infection BMJ 373:m1212, Pesch, M.H.,et al, 2021 Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Congenital Inflammatory Myopathy Neurol 40:1111-1114, Shevell,M.,et al, 1990 Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl Clin genet 37:355-362, Clarke,J.T.,et al, 1990 Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980 Showing articles 0 to 8 of 8