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Showing articles 0 to 8 of 8 Filter Applied: chromosome 19 (Click to remove) Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996 Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995 Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL) UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007 Clinical Spectrum of Episodic Ataxia Type 2 Neurol 62:17-22, Jen,J.,et al, 2004 Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13 Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999 Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 Showing articles 0 to 8 of 8