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Genetics of Cluster Headache Takes a Leap
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Familiality in Brain Tumors
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Parkinson Disease, 10 Years After Its Genetic Revolution: Multiple Clues to a Complex Disorder
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Collaborative Analysis of a-Synuclein Gene Promotor Variability and Parkinson Disease
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Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
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Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Complete Genomic Screen in Late-Onset Familial Alzheimer Disease, Evidence for a New Locus on Chromosome 12
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Kindreds of Dominantly Inherited Parkinson's Disease:Keys to the Riddle
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Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
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DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
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Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
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Fibromuscular Dysplasia and Its Neurologic Manifestations
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Clinical Genetics in Neurological Disease
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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