Atrophy of Bilateral Extraocular Muscles
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Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995
Parkinsonism-Recognition and Differential Diagnosis
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Late-Onset Mitochondrial Myopathy
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Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
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Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995
The Natural History of Progressive Mutlifocal Leukoencephalopathy in Patients with AIDS
Clin Inf Dis 20:1305-1310, Fong,I.W.,et al, 1995
Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995
Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995
Systemic Sclerosis Sine Scleroderma:An Unusual Presentation in Scleroderma Renal Crisis
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Systemic Sclerosis (Scleroderma) :Clinical Management of Its Major Complications
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Intrathecal Baclofen Therapy in Stiff-Man Syndrome:A Double-blind, Placebo-controlled Trial
Neurol 45:1893-1897, Silbert,P.L.,et al, 1995
Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
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Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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Comparison of Triple Dose vs Std Dose Gadolinium-DTPA for Detect of MRI Enhanc Lesions in Pts with Primary Progr MS
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The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
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Diagnostic Value of Detecting JC Virus DNA in Cerebropsinal Fluid of Patients with Progressive Multifocal Leukoencephalopathy
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Extrapyramidal Symptoms in a BMT Recipient with Hyperintense Basal Ganglia and Elevated Manganese
Bone Marrow Transplantation 15:989-992, Fredstrom,S.,et al, 1995
Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
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Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
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Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
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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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Amyloidosis Causing A Progressive Myopathy
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Hypoglycaemia in Spinal Muscular Atrophy
Lancet 346:609-610, Bruce,A.K.,et al, 1995
Natural History in Proximal Spinal Muscular Atrophy
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Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Acute Bilateral Ophthalmoplegia Secondary to Metastatic Prostatic Carcinoma:Demonstr of Magnetic Resonance Imaging
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Stereotactic Ventral Pallidotomy for Parkinson's Disease
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Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
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X-Linked Pure Familial Spastic Paraparesis
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Spinal Dural Arteriovenous Fistula:The Pathology of Venous Hypertensive Myelopathy
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Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Low-Dose (7. 5mg) Oral Methotrexate Reduces the Rate of Progression in Chronic Progressive Multiple Sclerosis
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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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JC Virus DNA in CSF of HIV-Infected Pts:Predictive Value for Progressive Multifocal Leukoencephalopathy
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Progressive Multifocal Leukoencephalopathy:Unusual MR Findings
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Clinicopath Conf
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Neurofibromatosis Type 1:Pathologic Substrate of High-Signal-Intensity Foci in the Brain
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MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
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Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995
Reflex Sympathetic Dystrophy in Children
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The Prevention of Neurogenetic Disease
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