Focal Neurologic symptoms in hypercalcemia
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Spinal Muscular Atrophy
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A Child with Arthrogryposis
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A Child with Delayed Motor Milestones and Ptosis
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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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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Neurologic Aspects of Inflammatory Bowel Disease
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
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The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
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A Teenager with Shortness of Breath and Difficulty Walking
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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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A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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Inflammatory Muscle Diseases
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A 52-year-old Woman with Progressive Proximal Weakness
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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The Limbic-Girdle Muscular Dystrophies
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Proximal Paresis of the Upper Extremity in Patients With Stroke
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Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
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Clinicopath Conf., Colchicine Myoneuropathy
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
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Painful Proximal Diabetic Neuropathy:Inflammatory Nerve Lesions and Spontaneous Favorable Outcome
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AAEM Case Report#13:Diabetic Amyotrophy
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Erroneous Diagnosis Corrected After 28 Years
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
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Sudden Onset of Profound Weakness in a Toddler
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Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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The Bruns-Garland Syndrome (Diabetic Amyotrophy) , Revisited 100 Years Later
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Congenital Muscular Dystrophy
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Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
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Central Core Disease, Clinical Features in 13 Patients
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