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Showing articles 0 to 11 of 11 Filter Applied: chromosomal abnormality (Click to remove) CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis Neurol 78:1150-1156, Deiva,K.,et al, 2012 Neurologic Manifestations of von Hippel-Lindau Disease JAMA 300:1334-1342, Butman,J.A.,et al, 2008 Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families Ann Neurol 41:150-159, Heutnik,P.,et al, 1997 A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995 Colpocephaly:Clinical, Radiologic, & Pathogenetic Aspects Neurol 35:1594-1598, Herskowitz,J.,et al, 1985 The Lissencephaly, (Agyria) Syndrome in Siblings Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978 X-Linked Malformation of Neuronal Migration Neurol 47:331-339, Dobyns,W.B.,et al, 1996 Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus Neurol 45:1086-1091, Chabriat,H.,et al, 1995 Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature JNNP 59:579-585, Verin,M.,et al, 1995 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Showing articles 0 to 11 of 11