Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022
Churg-Strauss Syndrome, Clinical Study and Long-Term Follow-Up of 96 Patients
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Mitochondrial DNA and Disease
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
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Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
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Mendelian Etiologies of Stroke
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Extrapulmonary Manifestations of Sarcoidosis
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Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
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Current and Emerging Issues in Wilsons Disease
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A 63-Year-Old Woman Presenting with Bilateral Leg Pain
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Progressive Proximal Weakness in a 61-Year-Old Man
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A 61-Year-Old Woman with Acute Onset Dysgraphia
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Muscular Dystrophies
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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Hearing and Vision Loss in an Older Man
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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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Diagnostic Challenges in a Young Patient with Hypereosinophilia
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Cardiovascular Dysfunction in Multiple Sclerosis
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Clinical Outcomes after Neurogenic Stress Induced Cardiomyopathy in Aneurysmal Sub-Arachnoid Hemorrhage: A Prospective Cohort Study
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Progressive Development of Cardiomyopathy Following Altered Autonomic Activity in Status Epilepticus
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A 32-year-old Woman with Right-Sided Numbness and Word-Finding Difficulties
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A 52-year-old Woman with Progressive Proximal Weakness
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Alcohol and Alcoholism
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
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MELAS
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Guidelines for the Prevention of Stroke in Patients With Stroke or Transient Ischemic Attack: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association
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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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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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Autoimmune Targets of Heart and Skeletal Muscles in Myasthenia Gravis
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Extension of the Clinical Spectrum of Danon Disease
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Takotsubo Cardiomyopathy in Acute Ischemic Stroke
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An Unusual Cause of Cardioembolic Stroke
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Antithrombotic and Interventional Treatment Options in Cardioembolic Transient Ischaemic Attack and Ischaemic Stroke
JNNP 78:14-24, McCabe,D.J.H. &Rakhit,R.D., 2007
When the Worst Headache Becomes the Worst Heartache!
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Glycogen-Storage Disease Type II
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Mitochondrial DNA Polymerase-y and Human Disease
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Mitoxantrone Treatment of Multiple Sclerosis
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Sudden Cardiac Death in Myotonic Dystrophy Type 2
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The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
Neurol 60:1246-1251,1230, Poppe,M.,et al, 2003
Mitochondrial Respiratory-Chain Diseases
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Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
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Hypertrophic Cardiomyopathy A Systematic Review
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Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
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Cardiac Dysfunction in Neuromuscular Diseases
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