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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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A Genetic Study of Idiopathic Focal Dystonias
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Transient Tic Disorder and the Spectrum of Tourette's Syndrome
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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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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Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Thyrotoxic Periodic Paralysis
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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The Phenotypic Continuum of ATP1A3-Related Disorders
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
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Clinical Reasoning: A Teenager with Left Arm Weakness
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Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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Red Papules on the Tongue of a Patient with Hemiparesis
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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Chediak-Higashi Syndrome: Pathognomonic Feature
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
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Tuberous Sclerosis Complex: A Tale of Two Genes
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Decoding Cryptogenic Cardioembolism
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Amyotrophic Lateral Sclerosis
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Metabolic Disease and Stroke: MELAS
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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The Tuberous Sclerosis Complex
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Malignant Hyperthermia, Update on Susceptibility Testing
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Mental Retardation
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Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
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Hypertrophic Cardiomyopathy A Systematic Review
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The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
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Ion Channel Diseases:Episodic Disorders of the Nervous System
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Tourette Syndrome:Update and Review of the Literature
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
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