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Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
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Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
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A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
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Huntington Disease: Clinical Features and Diagnosis
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Spinal Muscular Atrophy A Timely Review
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Tuberous Sclerosis Complex: A Tale of Two Genes
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
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Facial Nerve is Liable to Pressure Palsy
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Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
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Creutzfeldt-Jakob Disease in a Young Woman
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Natural History in Proximal Spinal Muscular Atrophy
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Evidence That the Gene for Tuberous Sclerosis is on Chromosome 9
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