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Showing articles 0 to 13 of 13 Filter Applied: chromosomal abnormality (Click to remove) Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011 Decoding Cryptogenic Cardioembolism Ann Neurol 64:364-365, Meschia,J.F., 2008 Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope BMJ 326:1078-1079, Plunkett,A.,et al, 2003 Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus Neurol 45:1086-1091, Chabriat,H.,et al, 1995 Clinical Significance of Fetal Choroid Plexus Cysts Lancet 346:724-729, Gupta,J.K.,et al, 1995 Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL) Ann Neurol 38:817-824, Hutchinson,M.,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 Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991 Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred Wertelecki. W. , et al, NEJM 319:276-2838., , 1988 Showing articles 0 to 13 of 13