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A Child with Delayed Motor Milestones and Ptosis
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The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
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Familial Autoimmune Myasthenia Gravis:Report of Four Families
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Congenital Myasthenic Syndromes
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Familial Autoimmune Myasthenia Gravis
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Acetylcholine Receptor Antibodies in Juvenile Myasthenia Gravis
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Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
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Brain Tumors
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Epilepsy Octet, Epidemiology, Classification, Natural History, and Genetics of Epilepsy
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Genetic Factors in Myasthenia Gravis:A Family Study
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Myasthenia Gravis in Identical Twins
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Familial Infantile Myasthenia Gravis
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Myasthenia Gravis & Myasthenic Syndromes
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Neurologic Complications of Hyperthyroidism
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Clinical Syndromes of Myasthenia in Infancy & Childhood
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
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Cause of Weakness in Myasthenia Gravis
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Differential Diagnosis of Tremors
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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RNF213 Polymorphisms in Intracranial Artery Dissection
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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Safety and Efficacy of Staged, Bilateral Focused Ultrasound Thalamotomy in Essential Tremor, An Open-Label Clinical Trial
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Genome Sequencing in the NICU and PICU is Here to Stay
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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Cavernous Maliformations of the Central Nervous System
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Vascular Malformations of the Central Nervous System
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Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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