Motor Neuropathy Due to Docetaxel and Paclitaxel
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Adult-Onset MELAS
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Inclusion Body Myositis
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Acute Type II Myofiber Atrophy in Critical Illness
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Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
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Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Primary Prevention of Stroke
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Parkinsonism Unmasked by Lovastatin
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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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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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Inclusion Body Myositis and Myopathies
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Apolipoprotein E E4 in Inclusion Body Myositis
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Lipoprotein (a) & Asympt Carotid Art Disease:Evidence of a Prominent Role in the Evol of Advanced Carotid Plaques
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Plasma Concentration of Lipoprotein (a) and the Risk of Future Stroke
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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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Lyme Neuroborreliosis
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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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Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
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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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Neurologic Aspects of Inflammatory Bowel Disease
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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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Late-Onset Mitochondrial Myopathy
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Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
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Anticonvulsant Hypersensitivity Syndrome
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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The Nondystrophic Myotonias
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HMG-CoA Reductase Inhibitor Therapy and Peripheral Neuropathy
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Posttraumatic Headache
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Mild Head Injury
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Peripheral Neuropathy with Bezafibrate
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Neuropathy Associated with Hyperlipidemia
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Becker Muscular Dystrophy with Onset after 60 Years
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Neurologic Manifestations of HIV Infection
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Myotonic Dystrophy
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