Cerebral Involvement in McLeod Syndrome
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Molecular Genetics in Neurology
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Quadriceps Myopathy in Two Brothers
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A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
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A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
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Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
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A 36-Year-Old Man With Asymmetric Muscle Weakness
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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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"Boule Du Biceps" in Dysferlinopathy
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Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
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A 54-year-old man with Dyspnea and Muscle Weakness
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Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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Subacute Paresis in a 28-year-old man with HIV
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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A 51-year-old Woman with Weakness and Stiff Neck
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ICU-Acquired Weakness and Recovery from Critical Illness
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Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
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The Floppy Infant: Evaluation of Hypotonia
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Extension of the Clinical Spectrum of Danon Disease
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
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Paresis Acquired in the Intensive Care Unit
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Clinical and Genetic Aspects of Distal Myopathies
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Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
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Critical Illness Myopathy
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,et al, 1997
Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
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Acute Corticosteroid Myopathy in Intensive Care Patients
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Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Prolonged Paralysis After Neuromuscular Blockage
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Tibial Muscular Dystrophy
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Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
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Ipecac Myopathy and Cardiomyopathy
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Congenital Monomelic Hypertrophy with Progressive Myopathy
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Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
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Progressive Myopathy in Hyperkalemic Periodic Paralysis
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The Effects of Alcoholism on Skeletal and Cardiac Muscle
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Ethanol and the Nervous System
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