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A 52-year-old Woman with Progressive Proximal Weakness
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Electrophysiological Study with Prophylactic Pacing and Survival in Adults with Myotonic Dystrophy and Conduction System Disease
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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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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
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009
Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
NEJM 358:2688-2697, Groh,W.J.,et al, 2008
Cardiac Involvement in Patients With Limb-Girdle Muscular Dystrophy Type 2 and Becker Muscular Dystrophy
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Severe Cardiac Arrhythmias in Young Patients with Myotonic Dystrophy Type 1
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Sudden Cardiac Death in Myotonic Dystrophy Type 2
Neurol 63:2402-2404, Schoser,B.G.H.,et al, 2004
The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
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Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
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Cardiac Dysfunction in Neuromuscular Diseases
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Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
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Cardiac Involvement in Genetically Confirmed Facioscapulohumeral Muscular Dystrophy
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies
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Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
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Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
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Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993
Sudden Death of a Carrier of X-Linked Emery-Dreifuss Muscular Dystrophy
Ann Int Med 119:900-905, Fishbein,M.C.,et al, 1993
The Heart in Myotonic Dystrophy
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Ventricular Late Potentials in Myotonic Dystrophy
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Myotonic Heart Disease:A Clinical Follow-Up
Neurol 41:259-262, Hawley,R.J.,et al, 1991
Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990
Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989
Left Ventricular Thrombus and Systemic Emboli Complicating the Cardiomyopathy of Duchenne's Muscular Dystrophy
Arch Neurol 46:1249-1252, Gaffney,J.F.,et al, 1989
Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988
Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
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Cardiac Involvement in Myotonic Muscular Dystrophy
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Radionuclide Angiocardiographic Analysis of Myocardial Function in Myotonic Muscular Dystrophy
Neurol 33:657-660, Hartwign,G.B.,et al, 1983
Families with Myotonic Dystrophy with & without Cardiac Involvement
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Serial Two-dimensional Echocardiography in Duchenne Muscular Dystrophy
Neurol 32:1101-1105, Goldberg,S.J.,et al, 1982
An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982
Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
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Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
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Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
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Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021
Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020
Telemedicine in Neurology
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"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020
Duchenne Muscular Dystrophy
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