The Nondystrophic Myotonias
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Myotonic Dystrophy
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Electrodiagnosis of Neuromuscular Disease
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Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
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Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023
A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022
A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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A 10-Year-Old Girl with Muscle Stiffness
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A Case of Muscle Twitching with Psoriasis
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A Child with Arthrogryposis
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Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
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A Child with Delayed Motor Milestones and Ptosis
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A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016
A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014
Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
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A Fisherman Who Could Not Row
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Segmental Zoster Paresis of Limbs: Report of Three Cases and Review of Literature
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Case 35-2006: A Newborn Boy with Hypotonia
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Clinicopath Conf., Colchicine Myoneuropathy
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Erroneous Diagnosis Corrected After 28 Years
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Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
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Congenital Myasthenic Syndromes
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Myopathy in Human Immunodeficiency Virus-Infected Children Receiving Long-Term Zidovudine Therapy
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Congenital Inflammatory Myopathy
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Neuromuscular Diseases Associated with Human Immunodeficiency Virus Infection
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Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
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Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
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Isaac Syndrome with Laryngeal Involvement:An Unusual Presentation of Myokymia
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A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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Adult Onset Nemaline Myopathy
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The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
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