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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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Clinical Reasoning: A Teenager with Left Arm Weakness
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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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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Red Papules on the Tongue of a Patient with Hemiparesis
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Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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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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Decoding Cryptogenic Cardioembolism
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Metabolic Disease and Stroke: MELAS
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Malignant Hyperthermia, Update on Susceptibility Testing
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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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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 Inherited Ataxias and the New Genetics
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Acute Intermittent Porphyria
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
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Transient Tic Disorder and the Spectrum of Tourette's Syndrome
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Mendelian Etiologies of Stroke
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Central Core Disease, Clinical Features in 13 Patients
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Familial Recurrent Bell's Palsy with Ocular Motor Palsies
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Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
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The Malignant Hyperthermia Syndrome
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Emery-Dreifuss Muscular Dystrophy
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Familial Periodic Ataxia
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Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
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Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
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Abnormal Iris Vasculature in Myotonic Dystrophy
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