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Atypical Parkinsonian Syndromes: A General Neurologists Perspective
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Clinicopath Conf, Multiple-System Atrophy
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Constipation in Neurological Diseases
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Improved Accuracy of Clinical Diagnosis of Lewy Body Parkinson's Disease
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Survival of Patients with Pathologically Proven Multiple System Atrophy:A Meta-Analysis
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What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
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Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
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Intrathecal Administration of Autologous Mesenchymal Stem Cells in Multiple System Atrophy
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Stridor in Multiple System Atrophy
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Treatment of Multiple System Atrophy Using Intravenous Immunoglobulin
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Second Consensus Statement on the Diagnosis of Multiple System Atrophy
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Morning Glory Sign: A Particular MR Finding in Progressive Supranuclear Palsy
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Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
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Diffusion-weighted MRI Differentiates the Parkinson Variant of Multiple System Atrophy from PD
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T2-weighted MRI Differentiates Multiple System Atrophy from Parkinson's Disease
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Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
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Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
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Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
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Prevalence of Progressive Supranuclear Palsy and Multiple System Atrophy:A Cross-Sectional Study
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Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
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Sympathetic Cardioneuropathy in Dysautonomias
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Distinction of Idiopathic Parkinson's Dis from Multi-Syst Atrophy by Stim of Growth-Hormone Release w Clonidine
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Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
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Consensus Statement on the Definition of Orthostatic Hypotension, Pure Autonomic Failure, and Multiple System Atrophy
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Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
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Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
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Different of Multi Syst Atrophy from Idiopathic Parkinson's Disease Using Proton MR Spectroscopy
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
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PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995
Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
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The Motor Disorder of Multiple System Atrophy
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Analysis of the Prion Protein Gene in Thalamic Dementia
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Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
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Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
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A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
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Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
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