Acute Corticosteroid Myopathy in Intensive Care Patients
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Inflammatory Myopathy in Thyrotoxicosis
Neurol 48:339-341, Hardiman,O.,et al, 1997
A 9-Year-Old With Fever and Severe Muscle Pains
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Motor Neuron Syndromes in Cancer Patients
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Gluteal Compartment Syndrome Due to Rhabdomyolysis After Heroin Abuse
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Muscle-Eye-Brain Disease:A Neuropathological Study
Ann Neurol 41:173-180, Haltia,M.,et al, 1997
Evaluation of Neuromuscular Symptoms in Veterans of the Persian Gulf War
Neurol 48:4-12, Amato,A.A.,et al, 1997
Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996
Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996
Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996
Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996
Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
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Bent Spine Syndrome
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Exacerbation of Myasthenia Gravis Associated with Cocaine Use
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Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996
Clinical Heterogeneity of Adhalin Deficiency
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Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
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A Woman with a Relapsing Psychosis Who Got Better with Prednisone
Lancet 347:1288, Cohen,L.,et al, 1996
Investigation of Muscle Disease
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Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Multifocal Motor Neuropathy with Conduction Block:A Study of 24 Patients
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Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995
Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995
Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995
Lambert-Eaton Myasthenic Syndrome:Clinical Diagnosis,Immune-Mediated Mechanisms,and Update on Therapies
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Polyarteritis Nodosa-Induced Quadriplegia
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Ocular Myasthenia:A Protean Disorder
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Myotonic Dystrophy
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The Nondystrophic Myotonias
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Cerebral Involvement in McLeod Syndrome
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994
A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
NEJM 330:585-591, Bensimon,G.,et al, 1994
Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
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Intravenous Immunoglobulin Trtm in Pts with Motor Neuron Syndromes Assoc with Anti-GM Antibodies:A Contrld Study
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Cardiac Injury Associated with Neurogenic Pulmonary Edema Following Subarachnoid Hemorrhage
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Acute Rhabdomyolysis in Patients Infected by Human Immunodeficiency Virus
Neurol 44:1692-1696, Chariot,P.,et al, 1994
Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
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Benign Familial Disease with Muscle Mounding and Rippling
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Anti-Ri Antibodies Associated with Opsoclonus and Progressive Encephalomyelitis with Rigidity
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Myasthenia Gravis
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Congenital Myasthenic Syndromes
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Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
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Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993
Myopathy in the Elderly:Evaluation of the Histopathologic Spectrum and the Accuracy of Clinical Diagnosis
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Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
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Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
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