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When the Worst Headache Becomes the Worst Heartache!
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A 61-Year-Old Woman with Acute Onset Dysgraphia
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A Boy with Heart Failure, A Thick Tongue, and Double Vision
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Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
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Recurrent Embolic Stroke and Cocaine-Related Cardiomyopathy
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Stroke in Pediatric Acquired Immunodeficiency Syndrome
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Embolic Stroke After Smoking"Crack"Cocaine
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Mendelian Etiologies of Stroke
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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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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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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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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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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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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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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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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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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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