Assessing disease progression with MRI in atypical parkinsonian disorders
Identifieur interne : 002447 ( Main/Exploration ); précédent : 002446; suivant : 002448Assessing disease progression with MRI in atypical parkinsonian disorders
Auteurs : Martin Köllensperger [Autriche] ; Gregor K. Wenning [Autriche]Source :
- Movement Disorders [ 0885-3185 ] ; 2009.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- DLB, Disease Progression, Humans, Lewy Body Disease (pathology), MRI, MSA, Magnetic Resonance Imaging (methods), Multiple System Atrophy (pathology), Nervous system diseases, Nuclear magnetic resonance imaging, PSP, Parkinson Disease (diagnosis), Parkinson Disease (pathology), Parkinson disease, Supranuclear Palsy, Progressive (pathology), disease progression.
- MESH :
- diagnosis : Parkinson Disease.
- methods : Magnetic Resonance Imaging.
- pathology : Lewy Body Disease, Multiple System Atrophy, Parkinson Disease, Supranuclear Palsy, Progressive.
- Disease Progression, Humans.
Abstract
During the last decade, novel MR techniques have become available to support the early differential diagnosis of Parkinsonism and also to generate MR surrogate markers of disease progression. The article reviews the current state of the art focusing on three atypical parkinsonian disorders: multiple system atrophy (MSA), progressive supranuclear palsy (PSP), and dementia with Lewy bodies (DLB). © 2009 Movement Disorder Society
Url:
DOI: 10.1002/mds.22582
Affiliations:
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Le document en format XML
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<term>Multiple System Atrophy (pathology)</term>
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<front><div type="abstract" xml:lang="en">During the last decade, novel MR techniques have become available to support the early differential diagnosis of Parkinsonism and also to generate MR surrogate markers of disease progression. The article reviews the current state of the art focusing on three atypical parkinsonian disorders: multiple system atrophy (MSA), progressive supranuclear palsy (PSP), and dementia with Lewy bodies (DLB). © 2009 Movement Disorder Society</div>
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