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Showing articles 0 to 10 of 10 Filter Applied: chromosomal abnormality (Click to remove) Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency Neurol 60:1413-1417, Pearl,P.L.,et al, 2003 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 Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987 Huntington Disease: Clinical Features and Diagnosis UptoDate Dec 2017, Oksana Suchowersky, 2017 Neurofibromatosis Type 2 Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009 Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Showing articles 0 to 10 of 10