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Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neurodegeneration with Brain Iron Accumulation
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Neuroimaging Changes in Menkes Disease, Part 1
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Huntington Disease: Clinical Features and Diagnosis
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Characyeristic features and progression of abnormalities on MRI for CARASIL
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Genetic Aspects of Alzheimer Disease
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Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
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Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
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New Players in the Genetics of Stroke
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Genetic Testing in Spinocerebellar Ataxias
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Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Clinical Genetics in Neurological Disease
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Molecular Genetic Advances in Fragile X Syndrome
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The DNA Laboratory and Neurolgoical Practice
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Molecular Genetics in Neurology
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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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Copper-Histidine Therapy for Menkes Disease
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Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
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Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
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Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
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Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
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Detecting Susceptibility to Malignant Hyperthermia
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The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
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Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
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Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
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The Triumph of Linkage Analysis, Editorial
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Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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Spinal Muscular Atrophies
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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