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Neuromyelitis Optica Spectrum Disorders
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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Familial Neuromyelitis Optica
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008
Parental Transmission of MS in a Population-Based Canadian Cohort
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Migraine and Cerebral White Matter Lesions
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
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Hereditary Form of Parkinsonism-Dementia
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The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
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Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
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Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
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Offspring Recurrence Rates and Clinical Characteristics of Conjugal Multiple Sclerosis
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Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Evidence for Genetic Basis of Multiple Sclerosis
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Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
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Tourette's Syndrome:A Model Neuropsychiatric Disorder
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The British Isles Survey of Multiple Sclerosis in Twins
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
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Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
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Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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