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A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Cancer Risk in Patients with Muscular Dystrophy and Myotonic Dystrophy
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Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022
Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Telemedicine in Neurology
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"Boule Du Biceps" in Dysferlinopathy
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Duchenne Muscular Dystrophy
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Accuracy of a Machine Learning Muscle MRI - Based Tool for the Diagnosis of Muscular Dystrophies
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Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
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Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
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Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
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Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
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Long-term Effects of Glucocorticoids on Function, Quality of Life, and Survival in Patients with Duchenne Muscular Dystrophy: A Prospective Cohort Study
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Persistent Respiratory Failure Following Cardiac Arrest
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Brain Imaging in Myotonic Dystrophy Type 1
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A 30-year-old Man with Progressive Weakness and Atrophy
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Mechanisms, Causes, and Effects of Hypercapnia
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A Neonate with Micrognathia and Hypotonia
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Efficacy of Idebenone on Respiratory Function in Patients with Duchenne Muscular Dystrophy not using Glucocorticoids (DELOS): A Double-Blind Randomised Placebo-Controlled Phase 3 Trial
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A 52-year-old Woman with Progressive Proximal Weakness
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The Limbic-Girdle Muscular Dystrophies
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Palliative Care and Neurology
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Electrophysiological Study with Prophylactic Pacing and Survival in Adults with Myotonic Dystrophy and Conduction System Disease
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Evidence-Based Path to Newborn Screening for Duchenne Muscular Dystrophy
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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Cancer Risk Among Patients with Myotonic Muscular Dystrophy
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
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Muscle Histology vs MRI in Duchenne Muscular Dystrophy
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Transition to Adult Care for Children with Chronic Neurological Disorders
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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Mexiletine Is an Effective Antimyotonia Treatment in Myotonic Dystrophy Type 1
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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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Clinical Features of Facioscapulohumeral Muscular Dystrophy 2
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Diagnosis and New Treatments in Muscular Dystrophies
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A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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The Floppy Infant: Evaluation of Hypotonia
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Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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