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Showing articles 0 to 14 of 14 Filter Applied: neurologic signs (Click to remove) Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Dopa-Responsive Dystonia Revisited Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012 Dystonia NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006 The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel NEJM 345:17-24,57, Ducros,A.,et al, 2001 Parkinson's Disease NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998 Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation JAMA 277:793-799, Lopera,F.,et al, 1997 X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997 Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia Neurol 49:1617-1620, Ragno,M.,et al, 1997 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 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 Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Migraine:Theories of Pathogenesis Lancet 339:1202-1207, Blau,J.N., 1992 Lisch Nodules in Neurofibromatosis Type I NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991 Showing articles 0 to 14 of 14