Zobrazeno 1 - 3
of 3
pro vyhledávání: '"diagnostic imaging [Stroke, Lacunar]"'
Autor:
Benno Gesierich, David G. Norris, Kim Wiegertjes, Rainer Malik, Marco Duering, José P. Marques, Marek J. Konieczny, Olaf Dietrich, Reinhold Schmidt, Anna Dewenter, Michael Ewers, Mathias Hübner, Sofia Finsterwalder, Frank-Erik de Leeuw, Anil M. Tuladhar, Annemieke ter Telgte, Anna Kopczak, Alexandra Koch
Publikováno v:
Neurology 96(5), 10.1212/WNL.0000000000011213-(2021). doi:10.1212/WNL.0000000000011213
Neurology, 96, E698-E708
Neurology, 96, 5, pp. E698-E708
Neurology, 96, E698-E708
Neurology, 96, 5, pp. E698-E708
ObjectiveTo test the hypothesis that multi-shell diffusion models improve the characterization of microstructural alterations in cerebral small vessel disease (SVD), we assessed associations with processing speed performance, longitudinal change, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::043dce13c302d519e4bb975c329c5444
Autor:
Martin Dichgans, Marco Duering, Hugues Chabriat, Eric Jouvent, François De Guio, Ophélia Godin, Yifeng Ling, Dominique Hervé
Publikováno v:
Stroke 48(2), 283-289 (2017). doi:10.1161/STROKEAHA.116.015750
Background and Purpose— Previous studies in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy showed that accumulation of lacunes strongly relate to clinical severity. However, the potential predictors of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1107edfbbd7920b738b166908230756
https://doi.org/10.1161/strokeaha.116.015750
https://doi.org/10.1161/strokeaha.116.015750
Autor:
Traylor, M, Tozer, D, Croall, I, Lisiecka-Ford, D, Olorunda, A, Boncoraglio, G, Dichgans, M, Lemmens, R, Rosand, J, Rost, N, Rothwell, P, Sudlow, C, Thijs, V, Rutten-Jacobs, L, Markus, H, Consortium, International Stroke Genetics
Publikováno v:
Neurology 92(8), e749-e757 (2019). doi:10.1212/WNL.0000000000006952
Objective To identify novel genetic associations with white matter hyperintensities (WMH). Methods We performed a genome-wide association meta-analysis of WMH volumes in 11,226 individuals, including 8,429 population-based individuals from UK Biobank
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::86b1590a97ab8889eac0af147f0e242f