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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Duchenne Muscular Dystrophy
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Muscular Dystrophies
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Palliative Care and Neurology
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The Limbic-Girdle Muscular Dystrophies
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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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Clinical Features of Facioscapulohumeral Muscular Dystrophy 2
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Diagnosis and New Treatments in Muscular Dystrophies
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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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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Gene Therapy for Duchenne Muscular Dystrophy: Expectations and Challenges
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Congenital Muscular Dystrophy
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Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
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The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
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Polymyositis and Dermatomyositis
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Clinical and Genetic Aspects of Distal Myopathies
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New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
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Cardiac Dysfunction in Neuromuscular Diseases
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Age and Cause of Death in Mitochondrial Diseases
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Antithrombotic Therapy to Prevent Stroke in Patients with Atrial Fibrillation:A Meta-Analysis
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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The Muscular Dystrophies
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Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
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Palliative Care in Neurology
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Pure Motor Hand Weakness
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Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Investigation of Muscle Disease
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The Prevention of Neurogenetic Disease
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Mitochondrial DNA and Disease
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Trinucleotide Repeat Expansion in Neurological Disease
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Myotonic Dystrophy
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Molecular Genetics in Neurology
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The Polymerase Chain Reaction:Application to Nervous System Disease
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The Heart in Myotonic Dystrophy
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Fasioscapulohumeral and Scapuloperoneal Syndromes
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Genetic Linkage in Neurologic Diseases
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Treatment of Myotonia
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Cardiac Involvement in Myotonic Muscular Dystrophy
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