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Yasmine T Asi

Showing results (1-10 of 13) with videos related to

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Brain Pathology (Zurich, Switzerland)|September 22, 2012
Identification and quantification of oligodendrocyte precursor cells in multiple system atrophy, progressive supranuclear palsy and Parkinson's diseaseZeshan Ahmed, Yasmine T Asi, Andrew J Lees, et al.
Brain : a Journal of Neurology|July 11, 2019
Improving diagnostic accuracy of multiple system atrophy: a clinicopathological studyYasuo Miki, Sandrine C Foti, Yasmine T Asi, et al.
Glia|March 5, 2014
Alpha-synuclein mRNA expression in oligodendrocytes in MSAYasmine T Asi, Julie E Simpson, Paul R Heath, et al.
Brain : a Journal of Neurology|May 10, 2020
Hippocampal α-synuclein pathology correlates with memory impairment in multiple system atrophyYasuo Miki, Sandrine C Foti, Daniela Hansen, et al.
Acta Neuropathologica|February 14, 2013
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?Aoife P Kiely, Yasmine T Asi, Eleanna Kara, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2015
Minimal change multiple system atrophy: an aggressive variant?Helen Ling, Yasmine T Asi, Igor N Petrovic, et al.
Acta Neuropathologica Communications|July 2, 2017
Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar DegenerationYvonne S Davidson, Andrew C Robinson, Louis Flood, et al.
Brain : a Journal of Neurology|April 6, 2021
Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsyYasuo Miki, Eiki Tsushima, Sandrine C Foti, et al.
Molecular Neurodegeneration|August 27, 2015
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutationAoife P Kiely, Helen Ling, Yasmine T Asi, et al.
Nature Neuroscience|December 19, 2018
TDP-43 extracted from frontotemporal lobar degeneration subject brains displays distinct aggregate assemblies and neurotoxic effects reflecting disease progression ratesFlorent Laferrière, Zuzanna Maniecka, Manuela Pérez-Berlanga, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Brain Pathology (Zurich, Switzerland)|September 22, 2012
Identification and quantification of oligodendrocyte precursor cells in multiple system atrophy, progressive supranuclear palsy and Parkinson's diseaseZeshan Ahmed, Yasmine T Asi, Andrew J Lees, et al.
Brain : a Journal of Neurology|July 11, 2019
Improving diagnostic accuracy of multiple system atrophy: a clinicopathological studyYasuo Miki, Sandrine C Foti, Yasmine T Asi, et al.
Glia|March 5, 2014
Alpha-synuclein mRNA expression in oligodendrocytes in MSAYasmine T Asi, Julie E Simpson, Paul R Heath, et al.
Brain : a Journal of Neurology|May 10, 2020
Hippocampal α-synuclein pathology correlates with memory impairment in multiple system atrophyYasuo Miki, Sandrine C Foti, Daniela Hansen, et al.
Acta Neuropathologica|February 14, 2013
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?Aoife P Kiely, Yasmine T Asi, Eleanna Kara, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2015
Minimal change multiple system atrophy: an aggressive variant?Helen Ling, Yasmine T Asi, Igor N Petrovic, et al.
Acta Neuropathologica Communications|July 2, 2017
Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar DegenerationYvonne S Davidson, Andrew C Robinson, Louis Flood, et al.
Brain : a Journal of Neurology|April 6, 2021
Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsyYasuo Miki, Eiki Tsushima, Sandrine C Foti, et al.
Molecular Neurodegeneration|August 27, 2015
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutationAoife P Kiely, Helen Ling, Yasmine T Asi, et al.
Nature Neuroscience|December 19, 2018
TDP-43 extracted from frontotemporal lobar degeneration subject brains displays distinct aggregate assemblies and neurotoxic effects reflecting disease progression ratesFlorent Laferrière, Zuzanna Maniecka, Manuela Pérez-Berlanga, et al.
Pageof 2