Zobrazeno 1 - 5
of 5
pro vyhledávání: '"genetics [Cerebral Hemorrhage]"'
Autor:
Martin Dichgans, Jordi Merino, Rainer Malik, Jose C. Florez, Catherine Sudlow, Bailey Montgomery, Jonathan Rosand, Sandro Marini, Dipender Gill, Christopher D. Anderson
Publikováno v:
Annals of neurology 87(4), 516-524 (2020). doi:10.1002/ana.25686
Marini, S, Merino, J, Montgomery, B E, Malik, R, Sudlow, C L, Dichgans, M, Florez, J C, Rosand, J, Gill, D & Anderson, C D 2020, ' Mendelian randomization study of obesity and cerebrovascular disease ', Annals of Neurology . https://doi.org/10.1002/ana.25686
Ann Neurol
Marini, S, Merino, J, Montgomery, B E, Malik, R, Sudlow, C L, Dichgans, M, Florez, J C, Rosand, J, Gill, D & Anderson, C D 2020, ' Mendelian randomization study of obesity and cerebrovascular disease ', Annals of Neurology . https://doi.org/10.1002/ana.25686
Ann Neurol
Objective To systematically investigate causal relationships between obesity and cerebrovascular disease and the extent to which hypertension and hyperglycemia mediate the effect of obesity on cerebrovascular disease. Methods We used summary statisti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20f4cfd4a82b54082ab08ccaaa4e0043
https://doi.org/10.1002/ana.25686
https://doi.org/10.1002/ana.25686
Autor:
Eric L. Harshfield, Claudia Langenberg, Marios K. Georgakis, Rainer Malik, Nora Franceschini, Hugh S. Markus, Nicholas J. Wareham, Martin Dichgans
Publikováno v:
Neurology
Neurology 96(13), e1732-e1742 (2021). doi:10.1212/WNL.0000000000011555
medRxiv
Neurology 96(13), e1732-e1742 (2021). doi:10.1212/WNL.0000000000011555
medRxiv
RationaleType 2 diabetes mellitus (T2D) is an established risk factor for cerebrovascular disease but the mechanisms underlying this association remain elusive. Disentangling the causal effects of T2D, hyperglycemia, and pre-diabetic phenotypes (insu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec726c2aae70696f78a316ee79c1810
Autor:
Jaeyoon Chung, Israel Fernandez-Cadenas, Matthew Traylor, Scott Silliman, Muralidharan Sargurupremraj, Joanna Pera, Rainer Malik, Agnieszka Slowik, Reinhold Schmidt, Christopher D. Anderson, Stéphanie Debette, Martin Dichgans, Devin L. Brown, Stacie L Demel, James F. Meschia, David L. Tirschwell, Jordi Jimenez-Conde, Bradford B. Worrall, Bo Norrving, Steffen Tiedt, Magdy Selim, Arne Lindgren, Steven M. Greenberg, Carl D. Langefeld, Jonathan Rosand, Jaume Roquer, Daniel Woo, Sandro Marini
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2019, 142 (10), pp.3176-3189. ⟨10.1093/brain/awz233⟩
Brain
Brain 142(10), 3176-3189 (2019). doi:10.1093/brain/awz233
Brain-A Journal of Neurology, Oxford University Press (OUP), 2019, 142 (10), pp.3176-3189. ⟨10.1093/brain/awz233⟩
Brain
Brain 142(10), 3176-3189 (2019). doi:10.1093/brain/awz233
Intracerebral haemorrhage and small vessel ischaemic stroke (SVS) are the most acute manifestations of cerebral small vessel disease, with no established preventive approaches beyond hypertension management. Combined genome-wide association study (GW
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc818cd1b714e742bcd83325f91f7f6e
https://hal.archives-ouvertes.fr/hal-03209579
https://hal.archives-ouvertes.fr/hal-03209579
Autor:
Israel Fernandez-Cadenas, Chia-Ling Phuah, Jeremiasz M. Jagiella, Agnieszka Slowik, Steven M. Greenberg, Tushar Dave, Joshua N. Goldstein, Bo Norrving, Miriam R. Raffeld, Christopher D. Anderson, Jaume Roquer, Natalia S. Rost, Anand Viswanathan, Arne Lindgren, Alexander Pichler, Joan Montaner, Daniel Woo, Braxton D. Mitchell, Carl D. Langefeld, Alessandro Biffi, Jordi Jimenez-Conde, Rainer Malik, Reinhold Schmidt, Alison M. Ayres, Martin Dichgans, Björn M. Hansen, B. B. Worrall, Steven J. Kittner, Christian Enzinger, Jonathan Rosand, Hugh S. Markus
Publikováno v:
Brain 140(10), 2663-2672 (2017). doi:10.1093/brain/awx220
Brain
Brain
Primary intracerebral haemorrhage and lacunar ischaemic stroke are acute manifestations of progressive cerebral microvascular disease. Current paradigms suggest atherosclerosis is a chronic, dynamic, inflammatory condition precipitated in response to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::257d3ec9481ed7dfe436a008a9ba22cb
https://ruj.uj.edu.pl/xmlui/handle/item/141524
https://ruj.uj.edu.pl/xmlui/handle/item/141524
Autor:
Stephan A. Kaeser, Astridur Palsdottir, Birkir Thor Bragason, Helgi J Isaksson, Angelos Skodras, Elias Olafsson, Asbjorg Osk Snorradottir
Publikováno v:
Brain research 1535, 106-114 (2013). doi:10.1016/j.brainres.2013.08.029
Hereditary Cystatin C Amyloid Angiopathy (HCCAA) is a rare genetic disease in Icelandic families caused by a mutation in the cystatin C gene, CST3. HCCAA is classified as a cerebral amyloid angiopathy and mutant cystatin C forms amyloid deposits in c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d673c028571863c6caa9c16089538df