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Showing articles 0 to 14 of 14 Filter Applied: hypotonia (Click to remove) Congenital Inflammatory Myopathy Neurol 40:1111-1114, Shevell,M.,et al, 1990 A Young Woman with Rapidly Progressive Weakness and Paresthesia Neurol 101:676-681, Alwakeel,S.S.,et al, 2023 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 Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization Arch Neurol 61:106-113, Guis,S.,et al, 2004 Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form Neurol 46:815-818, Kobayashi,O.,et al, 1996 Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Congenital Muscular Dystrophy J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989 Central Core Disease, Clinical Features in 13 Patients Medicine 66:389-396, Shuaid,A.,et al, 1987 Alternating Hemiplegia of Childhood Int Pediatr 2:115-119, Aicardi,J., 1987 Congenital Myotonic Dystrophy Arch Neurol 37:693-696, Argov,Z.,et al, 1980 Lumbosacral Radiculomyelitis Assoc with Pandemic Acute Hemorrhagic Conjunctivitis Letter Lancet Feb 1973., Wadia,N.H.,et al, 1973 Showing articles 0 to 14 of 14