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Showing articles 0 to 8 of 8 Filter Applied: chromosomal abnormality (Click to remove) Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Creutzfeldt-Jakob Disease in a Young Woman Lancet 347:945-948, Tabrizi,S.J.,et al, 1996 Familial Alzheimer's Disease Ann Neurol 36:335-336, Bird,T.D., 1994 Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994 Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description Ann Neurol 36:362-367, Haltia,M.,et al, 1994 Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993 Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients Neurol 41:1651-1655, Durner,M.,et al, 1991 Showing articles 0 to 8 of 8