Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
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Atrophy of Bilateral Extraocular Muscles
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Spinal Tract Pathology in AIDS:Postmortem MRI Correlation with Neuropathology
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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Apoliprprotein E E4 Allele & the Lifetime Risk of Alzheimer's Disease:What Physicians Know, & What They Should Know
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Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
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Common Variable Immunodeficiency and Inclusion Body Myositis:A Distinct Myopathy Mediated by Natural Killer Cells
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Amyloidosis Causing A Progressive Myopathy
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Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
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Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Acute Bacterial Myositis Due to Staphylococcus Aureus Septicemia
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Medical Complications During Stroke Rehabilitation
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Prolonged Paralysis After Neuromuscular Blockage
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The Prevention of Neurogenetic Disease
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Mild Traumatic Brain Injury:Pathophysiology, Natural History, and Clinical Management
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Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
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Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
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Mitochondrial DNA and Disease
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Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
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Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
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Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
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Relation of Alcoholic Myopathy to Cardiomyopathy
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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