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Metopropol For Essential Tremor
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Systemic Membrane Defect in the Proximal Muscular Dystrophies
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Familial Chorea & Myoclonus Epilepsy
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Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
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Diagnosis of Treatable Wilson's Disease
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Clinical Aspects of Spasmodic Dysphonia
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Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
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The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
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Familial Idiopathic Cerebral Calcifications
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Familial Essential Myoclonus
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Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
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Non-Beta Blocking Action of Propranolol
NEJM 293:988, Koch-Weser,J., 1975
Efficacy of Chronic Propranolol Therapy in Action Tremors of the Familial, Senile or Essential Varieties
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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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Clinicopathologic Conference, Posterior Reversible Encephalopathy Syndrome Due to Sickle Cell Disease
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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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RNF213 Polymorphisms in Intracranial Artery Dissection
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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 54-Year-Old Woman with Progressive Headache and Neurologic Decline
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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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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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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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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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Clinicopathologic Conference, Reversible Cerebral Vasoconstriction Syndrome with Takotsubo Cardiomyopathy
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Paraneoplastic Calmodulin Kinase-Like Vesicle-Associated Protein (CAMKV) Autoimmune Encephalitis
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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 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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