Search Results - "Teener, James W."
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Miller Fisher's syndrome
Published in Seminars in neurology (01-11-2012)“…Miller Fisher's syndrome is a rare variant of Guillain-Barré's syndrome characterized by the acute development of ataxia, ophthalmoparesis, and areflexia. Most…”
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Eculizumab for the treatment of glycine receptor antibody associated stiff-person syndrome
Published in Journal of neurology (01-09-2023)Get full text
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Electrophysiological Changes After Human Muscle Tear: A Potential Confounder
Published in American journal of physical medicine & rehabilitation (01-07-2020)“…ABSTRACTThe goal of this prospective electrophysiologic study is to describe the chronological electromyographic findings observed in a human gastrocnemius…”
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Late-onset Pompe's disease
Published in Seminars in neurology (01-11-2012)“…Glycogen storage disease type II, also known as Pompe's disease or acid maltase deficiency, is caused by a deficiency in acid α-glucosidase. Severe enzyme…”
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Stiff Person syndrome and other anti-GAD-associated neurologic disorders
Published in Seminars in neurology (01-11-2012)“…Antibodies directed against glutamic acid decarboxylase (GAD) are present in many patients with stiff person syndrome and increasingly found in patients with…”
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Maintenance plasma exchange treatment for muscle specific kinase antibody positive myasthenia gravis patients
Published in Journal of clinical apheresis (01-10-2015)“…Background:Anti‐muscle specific kinase antibody positive myasthenia gravis (MuSK MG) is often characterized by a relatively severe and progressive course,…”
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Inflammatory and toxic myopathy
Published in Seminars in neurology (01-11-2012)“…Although muscle diseases are relatively rare, several treatable myopathies must be recognized by the clinician to maximize the possibility of restoring…”
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Multifocal motor neuropathy
Published in Seminars in neurology (01-11-2012)“…Multifocal motor neuropathy is an acquired disorder in which demyelination of motor axons, presumably due to autoimmune attack, results in progressive painless…”
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Amyotrophic Lateral Sclerosis in a Patient with a Family History of Huntington Disease: Genetic Counseling Challenges
Published in Journal of genetic counseling (01-10-2014)“…Amyotrophic lateral sclerosis (ALS) and Huntington disease (HD) are generally considered to be distinct and easily differentiated neurologic conditions…”
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Dysregulation of sodium channel gating in critical illness myopathy
Published in Journal of muscle research and cell motility (01-05-2006)“…Critical illness myopathy (CIM) is the most common caused of acquired weakness in critically ill patients. While atrophy of muscle fibers causes weakness, the…”
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ECG changes during septic shock
Published in Cardiology (01-01-2002)“…We have previously found that skeletal muscle becomes electrically inexcitable in septic patients. Work in an animal model suggests that a decrease in the…”
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Chronic multiple paraneoplastic syndromes
Published in Muscle & nerve (01-11-2000)“…A patient presented with symptoms of limbic and brainstem encephalitis, motor and sensory neuronopathy, cerebellar dysfunction, and highly positive anti‐Hu…”
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Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome
Published in Experimental neurology (01-11-1989)“…A host protein encoded by the gene specifying the scrapie amyloid precursor affects pathogenesis of the transmissible spongiform encephalopathies:…”
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Polyneuropathy After Mechanical Ventilation
Published in JAMA : the journal of the American Medical Association (14-02-1996)“…To the Editor.—The article by Dr Leijten and colleagues1 merits comment. The authors studied 50 patients receiving mechanical ventilation for more than 7 days…”
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Möbius Syndrome With Oculomotor Nerve Paralysis Without Abducens Paralysis
Published in Journal of neuro-ophthalmology (01-12-1998)“…Möbius syndrome is typified by bilateral facial nerve palsies, usually with abducens palsies. We examined an infant with Möbius syndrome who had bifacial…”
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Direct muscle stimulation in acute quadriplegic myopathy
Published in Muscle & nerve (01-06-1997)“…We have previously found that muscle is electrically inexcitable in severe acute quadriplegic myopathy (AQM). In contrast, muscle retains normal electrical…”
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Treatment of Lambert-Eaton syndrome with intravenous immunoglobulin
Published in Muscle & nerve (01-05-1997)Get full text
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Bilateral trochlear nerve palsy and downbeat nystagmus in a patient with cephalic tetanus
Published in Neurology (01-09-1997)Get full text
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Muscle inexcitability in patients with reversible paralysis following steroids and neuromuscular blockade
Published in Muscle & nerve (01-09-1998)Get full text
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