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Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

Identifieur interne : 000A60 ( Ncbi/Curation ); précédent : 000A59; suivant : 000A61

Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

Auteurs : A. C. Ludolph [Allemagne] ; J. Kassubek [Allemagne] ; B. G. Landwehrmeyer [Allemagne] ; E. Mandelkow [Allemagne] ; E.-M. Mandelkow [Allemagne] ; D. J. Burn [Royaume-Uni] ; D. Caparros-Lefebvre [France] ; K. A. Frey [États-Unis] ; J. G. De Yebenes [Espagne] ; T. Gasser [Allemagne] ; P. Heutink [Pays-Bas] ; G. Höglinger [Allemagne] ; Z. Jamrozik [Pologne] ; K. A. Jellinger [Autriche] ; A. Kazantsev [États-Unis] ; H. Kretzschmar [Allemagne] ; A. E. Lang [Canada] ; I. Litvan [États-Unis] ; J. J. Lucas [Espagne] ; P. L. Mcgeer [Canada] ; S. Melquist [États-Unis] ; W. Oertel [Allemagne] ; M. Otto [Allemagne] ; D. Paviour [Royaume-Uni] ; T. Reum [Allemagne] ; A. Saint-Raymond [Royaume-Uni] ; J. C. Steele ; M. Tolnay [Suisse] ; H. Tumani [Allemagne] ; J. C. Van Swieten [Pays-Bas] ; M. T. Vanier [France] ; J.-P. Vonsattel [États-Unis] ; S. Wagner [Allemagne] ; Z. K. Wszolek [États-Unis]

Source :

RBID : PMC:2847416

Abstract

Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments within the central nervous system. These pathologic characteristics suggest shared pathogenetic pathways and possible molecular targets for disease-modifying therapeutic interventions. Natural history studies, for instance, in progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17, corticobasal degeneration, and Niemann-Pick disease type C as well as in amyotrophic lateral sclerosis/Parkinson–dementia complex permit clinical characterization of the disease phenotypes and are crucial to the development and validation of biological markers for differential diagnostics and disease monitoring, for example, by use of neuroimaging or proteomic approaches. The wide pathologic and clinical spectrum of the tauopathies with parkinsonism is reviewed in this article, and perspectives on future advances in the understanding of the pathogenesis are given, together with potential therapeutic strategies.


Url:
DOI: 10.1111/j.1468-1331.2008.02513.x
PubMed: 19364361
PubMed Central: 2847416

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J. C. Steele
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<title xml:lang="en" level="a" type="main">Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options</title>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
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<settlement type="city">Marbourg</settlement>
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<region type="district" nuts="2">District de Haute-Bavière</region>
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<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Centro de Biologica Molecular “Severo Ochoa,” Universidad Autonoma de Madrid and CiberNed, Cantoblanco, Madrid</wicri:regionArea>
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<nlm:aff id="A9">Philipps-Universität, Neurologie, Rudolf-Bultmann-Strasse, Marburg, Germany</nlm:aff>
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<name sortKey="Otto, M" sort="Otto, M" uniqKey="Otto M" first="M." last="Otto">M. Otto</name>
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<nlm:aff id="A1">Department of Neurology, University of Ulm, Ulm, Germany</nlm:aff>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurology, University of Ulm, Ulm</wicri:regionArea>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
<region type="district" nuts="2">District de Tübingen</region>
<settlement type="city">Ulm</settlement>
<settlement type="city">Ulm</settlement>
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<orgName type="university">Université d'Ulm</orgName>
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<author>
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<placeName>
<region type="country">Angleterre</region>
</placeName>
<wicri:cityArea>National Hospital for Neurology, Dementia Research Centre, London</wicri:cityArea>
</affiliation>
</author>
<author>
<name sortKey="Reum, T" sort="Reum, T" uniqKey="Reum T" first="T." last="Reum">T. Reum</name>
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<nlm:aff id="A20">Bundesinstitut für Arzneimittel & Medizinprodukte, Wissenschaftlicher Service/Klinische Prüfungen, Georg-Kiesinger-Allee, Bonn, Germany</nlm:aff>
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<region type="land" nuts="1">Rhénanie-du-Nord-Westphalie</region>
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</affiliation>
</author>
<author>
<name sortKey="Saint Raymond, A" sort="Saint Raymond, A" uniqKey="Saint Raymond A" first="A." last="Saint-Raymond">A. Saint-Raymond</name>
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<nlm:aff id="A21">European Medicines Agency (EMEA), Scientific Advice and Orphan Drugs Sector, 7 Westferry Circus, Canary Wharf, London, England</nlm:aff>
<country>Royaume-Uni</country>
<placeName>
<region type="country">Angleterre</region>
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<wicri:cityArea>European Medicines Agency (EMEA), Scientific Advice and Orphan Drugs Sector, 7 Westferry Circus, Canary Wharf, London</wicri:cityArea>
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</author>
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<nlm:aff id="A23">Institut für Pathologie, Schönbeinstrasse, Basel, Switzerland</nlm:aff>
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<name sortKey="Van Swieten, J C" sort="Van Swieten, J C" uniqKey="Van Swieten J" first="J. C." last="Van Swieten">J. C. Van Swieten</name>
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<nlm:aff id="A24">University Hospital Rotterdam, Department of Neurology, Erasmus MC, Dr Molewaterplein, GD Rotterdam, the Netherlands</nlm:aff>
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<name sortKey="Vanier, M T" sort="Vanier, M T" uniqKey="Vanier M" first="M. T." last="Vanier">M. T. Vanier</name>
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<nlm:aff id="A25">Institut National de la Santé et de la Recherche Médicale, Unit 820, Laeënnec Medical School, Lyon, France</nlm:aff>
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</author>
<author>
<name sortKey="Wszolek, Z K" sort="Wszolek, Z K" uniqKey="Wszolek Z" first="Z. K." last="Wszolek">Z. K. Wszolek</name>
<affiliation wicri:level="1">
<nlm:aff id="A28">Mayo Clinic, Department of Neurology, Jacksonville, FL, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Mayo Clinic, Department of Neurology, Jacksonville, FL</wicri:regionArea>
<wicri:noRegion>FL</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j">European journal of neurology : the official journal of the European Federation of Neurological Societies</title>
<idno type="ISSN">1351-5101</idno>
<idno type="eISSN">1468-1331</idno>
<imprint>
<date when="2009">2009</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p id="P2">Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments within the central nervous system. These pathologic characteristics suggest shared pathogenetic pathways and possible molecular targets for disease-modifying therapeutic interventions. Natural history studies, for instance, in progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17, corticobasal degeneration, and Niemann-Pick disease type C as well as in amyotrophic lateral sclerosis/Parkinson–dementia complex permit clinical characterization of the disease phenotypes and are crucial to the development and validation of biological markers for differential diagnostics and disease monitoring, for example, by use of neuroimaging or proteomic approaches. The wide pathologic and clinical spectrum of the tauopathies with parkinsonism is reviewed in this article, and perspectives on future advances in the understanding of the pathogenesis are given, together with potential therapeutic strategies.</p>
</div>
</front>
</TEI>
</record>

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