Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Dimitri, Hemelsoet"'
Autor:
Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, Sanne Steyaert, Rudy Van Coster, Paul J. Coucke, Wouter Steyaert, Bert Callewaert, Elke Bogaert, Patrick Verloo, Arnaud V. Vanlander, Elke Debackere, Jody Ghijsels, Pontus LeBlanc, Hannah Verdin, Leslie Naesens, Filomeen Haerynck, Steven Callens, Bart Dermaut, Bruce Poppe, for UD-PrOZA
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-13 (2022)
Abstract Background In order to facilitate the diagnostic process for adult patients suffering from a rare disease, the Undiagnosed Disease Program (UD-PrOZA) was founded in 2015 at the Ghent University Hospital in Belgium. In this study we report th
Externí odkaz:
https://doaj.org/article/132a277748754b7f9f15a3480f1078a1
Autor:
Sarah Dewilde, Lieven Annemans, Andrew Lloyd, Andre Peeters, Dimitri Hemelsoet, Yves Vandermeeren, Philippe Desfontaines, Raf Brouns, Geert Vanhooren, Patrick Cras, Boudewijn Michielsens, Patricia Redondo, Vincent Thijs
Publikováno v:
Health and Quality of Life Outcomes, Vol 17, Iss 1, Pp 1-11 (2019)
Abstract Background To estimate the additional impact of coping and of being dependent on caregivers, over and above the large effects of disability on utility after ischemic stroke. Methods A total of 539 patients were recruited into an observationa
Externí odkaz:
https://doaj.org/article/40e74338301e4f92a495c0ac335d97d3
Autor:
Timo Kahles, Patrik Michel, Alexander Hapfelmeier, Franz R. Eberli, Marialuisa Zedde, Vincent Thijs, Markus Kraemer, Stefan T. Engelter, Joaquin Serena, Christian Weimar, Achim Mallmann, Andreas Luft, Dimitri Hemelsoet, David E. Thaler, Andreas Müller-Eichelberg, Adinda De Pauw, Roman Sztajzel, Carmel Armon, David M. Kent, Bernhard Meier, Heinrich P. Mattle, Urs Fischer, Marcel Arnold, Marie-Luise Mono, Krassen Nedeltchev, for the International PFO Consortium NCT
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background and Purpose: To identify factors associated with prior stroke at presentation in patients with cryptogenic stroke (CS) and patent foramen ovale (PFO).Methods: We studied cross-sectional data from the International PFO Consortium Study (NCT
Externí odkaz:
https://doaj.org/article/6b4abb56191a49fea277ec3088b02b19
Autor:
Emilie De Muynck, Vincent Huybrechts, Dimitri Hemelsoet, Elisabeth Dhondt, Peter Vanlangenhove, Luc Defreyne
Publikováno v:
Journal of the Belgian Society of Radiology, Vol 104, Iss 1 (2020)
Background: Recently, CT perfusion (CTP) has been proposed as a selection tool for stroke patients to be treated with endovascular thrombectomy. We investigated whether functional outcome following endovascular treatment was improved after the introd
Externí odkaz:
https://doaj.org/article/8da80e86fa4144b1a7aab7bafb7a5f6d
Publikováno v:
TRENDS IN MOLECULAR MEDICINE
Moyamoya disease (MMD) is a rare cerebrovascular disorder with unknown etiology. MMD is characterized by progressive narrowing of arteries of the brain and the formation of a compensatory network of fragile vessels. Genetic studies have identified RN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cfdeece7349dca3cf8b2e0b290f792d
https://doi.org/10.1016/j.molmed.2022.08.009
https://doi.org/10.1016/j.molmed.2022.08.009
Autor:
Elke Bogaert, Aurore Garde, Thierry Gautier, Kathleen Rooney, Yannis Duffourd, Pontus LeBlanc, Emma van Reempts, Frederic Tran Mau-Them, Ingrid M. Wentzensen, Kit Sing Au, Kate Richardson, Hope Northrup, Vincent Gatinois, David Geneviève, Raymond J. Louie, Michael J. Lyons, Lone Walentin Laulund, Charlotte Brasch-Andersen, Trine Maxel Juul, Fatima El It, Nathalie Marle, Patrick Callier, Raissa Relator, Sadegheh Haghshenas, Haley McConkey, Jennifer Kerkhof, Claudia Cesario, Antonio Novelli, Nicola Brunetti-Pierri, Michele Pinelli, Perrine Pennamen, Sophie Naudion, Marine Legendre, Cécile Courdier, Aurelien Trimouille, Martine Doco Fenzy, Lynn Pais, Alison Yeung, Kimberly Nugent, Elizabeth R. Roeder, Tadahiro Mitani, Jennifer E. Posey, Daniel Calame, Hagith Yonath, Jill A. Rosenfeld, Luciana Musante, Flavio Faletra, Francesca Montanari, Giovanna Sartor, Alessandra Vancini, Marco Seri, Claude Besmond, Karine Poirier, Laurence Hubert, Dimitri Hemelsoet, Arnold Munnich, James R. Lupski, Christophe Philippe, Christel Thauvin-Robinet, Laurence Faivre, Bekim Sadikovic, Jérôme Govin, Bart Dermaut, Antonio Vitobello
Publikováno v:
AMERICAN JOURNAL OF HUMAN GENETICS
SRSF1 (also known as ASF/SF2) is a non-small nuclear ribonucleoprotein (non-snRNP) that belongs to the arginine/serine (R/S) domain family. It recognizes and binds to mRNA, regulating both constitutive and alternative splicing. The complete loss of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5551e236309b7081069f46ca7428ec
https://hdl.handle.net/1854/LU-01GYYM7M9B6XFW9NMT6Y4E6XMM
https://hdl.handle.net/1854/LU-01GYYM7M9B6XFW9NMT6Y4E6XMM
Autor:
Sven Dekeyzer, Stefanie Vanden Bossche, Vincent Keereman, Dimitri Hemelsoet, Veroniek Van Driessche
Publikováno v:
Journal of the Belgian Society of Radiology, Vol 99, Iss 2, Pp 85-89 (2015)
Both stroke and seizures have varied clinical presentations and their differentiation in the acute setting is not always straightforward. We present the case of a patient who presented at the emergency room with acute onset aphasia. Clinically acute
Externí odkaz:
https://doaj.org/article/b20fb60724674a0b98dc84c77db597a0
Publikováno v:
Acta Neurologica Belgica. 122:1111-1113
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e99938ad0707e932d3c420251df04882
https://doi.org/10.1007/s13760-022-01935-y
https://doi.org/10.1007/s13760-022-01935-y
Autor:
Julie De Zaeytijd, Paul Coucke, Lukas Nollet, Dimitri Hemelsoet, Laurence Campens, Bart P. Leroy, Olivier Vanakker
Publikováno v:
Journal of Medical Genetics. 59:496-504
BackgroundBiallelic pathogenic variants in the ATP-binding cassette subfamily C member 6 (ABCC6) gene cause pseudoxanthoma elasticum, a multisystemic ectopic calcification disorder, while heterozygous ABCC6 variants are associated with an increased r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb4f202b79a61fdb73ccaf43935a6e26
https://doi.org/10.1136/jmedgenet-2020-107565
https://doi.org/10.1136/jmedgenet-2020-107565
Autor:
Cathérine Dekeyser, Alexander Vanhoorne, Dimitri Hemelsoet, Liesbeth Van Hijfte, Julie De Zaeytijd, Veroniek Van Driessche, Helen Van Hoecke, Marijke Miatton, Tineke Van Vrekhem, Leen Maes, Guy Laureys
Publikováno v:
Journal of Neuroimmunology. 376:578032
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4268b39daea78cf8b61153029cb5ce74
https://doi.org/10.1016/j.jneuroim.2023.578032
https://doi.org/10.1016/j.jneuroim.2023.578032