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The Limbic-Girdle Muscular Dystrophies
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Inflammatory Myopathies with Anti-Ku Antibodies
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Inclusion Body Myositis, Observations in 40 Patients
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Eosinophilic Polymyositis
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Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023
Spinal Muscular Atrophy
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Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
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Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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A 42-year-old man with unilateral leg weakness
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Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
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A Child with Arthrogryposis
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A Child with Delayed Motor Milestones and Ptosis
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin E Deficiency
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Underappreciated Statin-Induced Myopathic Weakness Causes Disability
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Amyloid Myopathy Presenting with Distal Atrophic Weakness
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
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Steroid Myopathy in Cancer Patients
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Painful Proximal Diabetic Neuropathy:Inflammatory Nerve Lesions and Spontaneous Favorable Outcome
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Clinical Heterogeneity of Adhalin Deficiency
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AAEM Case Report#13:Diabetic Amyotrophy
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Motor Neuropathy Due to Docetaxel and Paclitaxel
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Erroneous Diagnosis Corrected After 28 Years
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Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992
Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992
Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
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McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992
Prognosis in AZT Myopathy
Neurol 41:1181-1184, Chalmers,A.C.,et al, 1991
Colchicine-Induced Myopathy and Neuropathy
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Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
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Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
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The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
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Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
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Spectrum of Inclusion Body Myositis
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Proximal Weakness of the Extremities as Main Feature of Amyloid Myopathy
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Colchicine Myopathy & Neuropathy
NEJM 316:1562-1568, Kuncl,R.W.,et al, 1987
Acid Maltase Deficiency
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Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
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Inclusion Body Myositis
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Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
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Eosinophilic Polymyositis
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Carnitine Deficiency Acute Postpartum Crisis
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