Movement Disorders (revue) - Checkpoint (Ncbi)

Index « Mesh.i » - entrée « Inclusion Bodies »
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Incidence < Inclusion Bodies < Income  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 23.
[0-20] [0 - 20][0 - 23][20-22][20-40]
Ident.Authors (with country if any)Title
000326 (2000) E. Jaros [Royaume-Uni] ; D J BurnThe pathogenesis of multiple system atrophy: past, present, and future.
000357 (2000) J D O'Sullivan [Royaume-Uni] ; H A Hanagasi ; S E Daniel ; P. Tidswell ; S W Davies ; A J LeesNeuronal intranuclear inclusion disease and juvenile parkinsonism.
000B47 (2003) Tamas Revesz [Royaume-Uni] ; Janice L. HoltonAnatamopathological spectrum of tauopathies.
000B50 (2003) Gregor K. Wenning [Autriche] ; Felix Geser ; Michaela Stampfer-Kountchev ; François TisonMultiple system atrophy: an update.
000B68 (2003) Ruth H. Walker [États-Unis] ; Paul F. Good ; P. ShashidharanTorsinA immunoreactivity in inclusion bodies in trinucleotide repeat diseases.
000C98 (2004) Richard A. Armstrong [Royaume-Uni] ; Peter L. Lantos ; Nigel J. CairnsSpatial patterns of alpha-synuclein positive glial cytoplasmic inclusions in multiple system atrophy.
000F57 (2005) Elsa Krim [France] ; Anne Vital ; Frederic Macia ; Farid Yekhlef ; François TisonAtypical parkinsonism combining alpha-synuclein inclusions and polyglucosan body disease.
001409 (2006) Juan J. Zarranz [Espagne] ; Juan C. G Mez-Esteban ; Bego A Atarés ; Elena Lezcano ; Maribel ForcadasTau-predominant-associated pathology in a sporadic late-onset Hallervorden-Spatz syndrome.
001904 (2006) Heiko Braak [Allemagne] ; Jürgen R. Bohl ; Christian M. Müller ; Udo Rüb ; Rob A I. De Vos ; Kelly Del TrediciStanley Fahn Lecture 2005: The staging procedure for the inclusion body pathology associated with sporadic Parkinson's disease reconsidered.
001909 (2006) Alberto J. Espay [Canada] ; Catherine Bergeron ; Robert Chen ; Anthony E. LangRapidly progressive sporadic dentatorubral pallidoluysian atrophy with intracytoplasmic inclusions and no CAG repeat expansion.
001979 (2007) Melissa J. Nirenberg [États-Unis] ; Jenny Libien ; Jean-Paul Vonsattel ; Stanley FahnMultiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation.
001E23 (2007) Yaroslau Compta [Espagne] ; Francesc Valldeoriola ; Eduardo Tolosa ; María Jesús Rey ; María José Martí ; Josep Valls-SoléLong lasting pure freezing of gait preceding progressive supranuclear palsy: a clinicopathological study.
002114 (2008) Christian Wider [États-Unis] ; Ryan J. Uitti ; Zbigniew K. Wszolek ; John Y. Fang ; Keith A. Josephs ; Matthew C. Baker ; Rosa Rademakers ; Michael L. Hutton ; Dennis W. DicksonProgranulin gene mutation with an unusual clinical and neuropathologic presentation.
002140 (1991) W R Gibb [Royaume-Uni] ; T. Scott ; A J LeesNeuronal inclusions of Parkinson's disease.
002428 (2009) Jason P. Covy [États-Unis] ; Wuxing Yuan [États-Unis] ; Elisa A. Waxman [États-Unis] ; Howard I. Hurtig [États-Unis] ; Vivianna M. Van Deerlin [États-Unis] ; Benoit I. Giasson [États-Unis]Clinical and Pathological Characteristics of Patients with Leucine-Rich Repeat Kinase-2 Mutations
003087 (2011) Giovanni Fabbrini [Italie] ; Marcello Merello ; Andrew H. Evans ; Andrew J. Lees ; Janice Holton ; David R. WilliamsProgressive parkinsonism, oculomotor abnormalities and autonomic dysfunction: clinicopathological case.
003224 (1990) A J Lewis [Canada] ; M J GawelDiffuse Lewy body disease with dementia and oculomotor dysfunction.
003B53 (2013) Alessandro Malandrini [Italie] ; Anna Rubegni ; Carla Battisti ; Gianna Berti ; Antonio FedericoElectron-dense lamellated inclusions in 2 siblings with Kufor-Rakeb syndrome.
003D46 (2014) Zhan-Fang Sun [République populaire de Chine] ; Xiao-Shuang Xiang ; Zhao Chen ; Li Zhang ; Bei-Sha Tang ; Kun Xia ; Hong JiangIncrease of the plasma α-synuclein levels in patients with multiple system atrophy.
003E92 (2014) Olivier Flabeau [France] ; Wassilios G. Meissner ; Annaig Ozier ; Patrick Berger ; François Tison ; Pierre-Olivier FernagutBreathing variability and brainstem serotonergic loss in a genetic model of multiple system atrophy.
004158 (1989) N P Quinn [Royaume-Uni] ; P. Luthert ; M. Honavar ; C D MarsdenPure akinesia due to lewy body Parkinson's disease: a case with pathology.

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