Differential (Click to cross reference) ataxia cerebellar ataxia, children children chromosomal abnormality chromosome 2 cognition developmental retardation Dravet syndrome familial fever gene mutation genetic neurologic disorders intellectual deficit mortality myoclonic jerks myoclonus myoclonus, epilepsy prognosis psychomotor retardation pyramidal tract dysfunction review article SCN1A gene seizure seizure, children seizure, familial seizure, febrile seizure, intractable seizure, neonatal seizure, tonic-clonic sodium channel dysfunction status epilepticus

Showing articles 1650 to 1661 of 1661 << Previous Ocular Myopathy Arch Neurol 20:1, Magora,A.,et al, 1969 The Oculopharyngeal Syndrome JAMA 203:1003, Murphy,S.F.,et al, 1968 Myopathy of the Quadriceps Muscles J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968 Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J. Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968 Huntington's Chorea Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968 Inherited Aminoacidopathies Demonstrating Vitamin Dependency NEJM 281:145, Rosenberg,L., 1965 Morquio's Disease, A Radiologic & Morphologic Study Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964 Familial and Conjugal Multiple Sclerosis Brain 86:315-332, Schapira,K.,et al, 1963 The Cornelia de Lange Syndrome J Pediatr 63:1000-1020, Ptacek,L.J., 1963 Angiokeratoma Corporis Diffusum Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962 Microcephaly Arch Dis Child 37:623-627, Davies,H.,et al, 1962 Clinical Study of Nine Patients with ReNU Syndrome , Okamoto,N.,et al, Showing articles 1650 to 1661 of 1661 << Previous