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Spinal Muscular Atrophy
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Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
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Telemedicine in Neurology
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Recurrent Cerebral Ischemia During Pregnancies
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Differentiation Between Traumatic Tap and Aneurysmal Subarachnoid Hemorrhage: Prospective Cohort Study
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Differential Features of Carotid and Vertebral Artery Dissections
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Sports-Related Internal Carotid Artery Dissection: Pathogenesis and Therapeutic Point of View
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The Tuberous Sclerosis Complex
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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The DYT1 Phenotype and Guidelines for Diagnostic Testing
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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The Muscular Dystrophies
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
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Apolipoprotein E Genotyping in Alzheimer's Disease
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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The DNA Laboratory and Neurolgoical Practice
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Unstable DNA Sequence in Myotonic Dystrophy
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Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
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Genetic Diagnosis of Gaucher's Disease
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Lisch Nodules in Neurofibromatosis Type I
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Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
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Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
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Guidelines in Action: Worse Headache of Life...Yesterday
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Consensus Practice Guidelines on Postdural Puncture Headache from a Multisociety, International Working Group
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An 8-Year-Old with Acute Onset Ataxia
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Updates on Sturge-Weber Syndrome
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National Institute of Neurological Disorders and Stroke Consensus Diagnostic Criteria for Traumatic Encephalopathy Syndrome
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Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
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Reversible Cerebral Vasoconstriction Syndrome
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