A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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RNF213 Polymorphisms in Intracranial Artery Dissection
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Thyrotoxic Periodic Paralysis
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Amyotrophic Lateral Sclerosis
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Alzheimers Disease
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Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
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Genetics of Cluster Headache Takes a Leap
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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Genomewide Association Studies of Stroke
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Autism
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Decoding Cryptogenic Cardioembolism
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A Genetic Risk Factor for Periodic Limb Movements in Sleep
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Parkinson Disease, 10 Years After Its Genetic Revolution: Multiple Clues to a Complex Disorder
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
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Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
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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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Stroke in Williams Syndrome
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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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Increased Risk of Alzheimer's Disease in Mothers of Adults with Down's Syndrome
Lancet 344:353-356, Schupf,N.,et al, 1994
DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
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Migraine:Theories of Pathogenesis
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Risk Factors for Multiple Sclerosis:Race or Place? Editorial
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Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
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