Progressive Encephalomyelitis with Rigidity Responsive to Plasmapheresis and Immunosuppression
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Motor Neuron Disease with Parkinsonism
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Bent Spine Syndrome
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
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Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996
Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
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The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Clinicopath Conf
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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X-Linked Pure Familial Spastic Paraparesis
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995
Late-Onset Mitochondrial Myopathy
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Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995
Reflex Sympathetic Dystrophy in Children
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Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
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Mitochondrial DNA and Disease
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Amyloidosis Causing A Progressive Myopathy
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Hypoglycaemia in Spinal Muscular Atrophy
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Natural History in Proximal Spinal Muscular Atrophy
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Polyarteritis Nodosa-Induced Quadriplegia
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Growth Factors:Potential Therapeutic Applications in Neurology
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Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994
Detection of Cortical Neuron Loss in Motor Neuron Disease by Proton Magnetic Resonance Spectroscopic Imaging in Vivo
Neurol 44:1933-1938, Pioro,E.P.,et al, 1994
Superoxide Dismutase and ALS
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Monomelic Amyotrophy
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Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994
Neurologic Manifestations of HIV Infection
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Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
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Myotonic Dystrophy
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Botulinum Toxin-A Improves the Rigidity of Progressive Supranuclear Palsy
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The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
Ann Neurol 35:234-237, Kornberg,A.J.,et al, 1994
Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
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A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
NEJM 330:585-591, Bensimon,G.,et al, 1994
Conjugal Amyotrophic Lateral Sclerosis:A Report on Two Couples from Southern France
Neurol 44:547-548, Camu,W.,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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Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
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Osteomalacic Myopathy
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Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
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