Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Lindsay Poppe"'
Autor:
Flor Verghote, Lindsay Poppe, Sofie Verbeke, Piet Dirix, Maarten Albersen, Gert De Meerleer, Charlien Berghen, Piet Ost, Geert Villeirs, Pieter De Visschere, Kathia De Man, Daan De Maeseneer, Sylvie Rottey, Charles Van Praet, Karel Decaestecker, Valérie Fonteyne
Publikováno v:
BMC Cancer, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background The outcome of patients with muscle-invasive bladder cancer (MIBC) remains poor, despite aggressive treatments. Inadequate primary staging, classically performed by computed tomography (CT)-imaging, could lead to inappropriate tre
Externí odkaz:
https://doaj.org/article/bb6642d943504af999d236b8d42f9b98
Autor:
Lindsay Poppe, Laura Rué, Mieke Timmers, Annette Lenaerts, Annet Storm, Zsuzsanna Callaerts-Vegh, Gilles Courtand, Antina de Boer, Silke Smolders, Philip Van Damme, Ludo Van Den Bosch, Rudi D’Hooge, Bart De Strooper, Wim Robberecht, Robin Lemmens
Publikováno v:
Alzheimer’s Research & Therapy, Vol 11, Iss 1, Pp 1-13 (2019)
Abstract Background EphA4 is a receptor of the ephrin system regulating spine morphology and plasticity in the brain. These processes are pivotal in the pathophysiology of Alzheimer’s disease (AD), characterized by synapse dysfunction and loss, and
Externí odkaz:
https://doaj.org/article/0285cce7c3524e97916463b91189a49d
Autor:
Laura Rué, Patrick Oeckl, Mieke Timmers, Annette Lenaerts, Jasmijn van der Vos, Silke Smolders, Lindsay Poppe, Antina de Boer, Ludo Van Den Bosch, Philip Van Damme, Jochen H. Weishaupt, Albert C. Ludolph, Markus Otto, Wim Robberecht, Robin Lemmens
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-15 (2019)
Abstract Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that affects motor neurons in the brainstem, spinal cord and motor cortex. ALS is characterized by genetic and clinical heterogeneity, suggesting the existence of genet
Externí odkaz:
https://doaj.org/article/7687f003c5824b29951e2494d1c45936
Autor:
Lindsay Poppe, Silke Smolders, Laura Rué, Mieke Timmers, Annette Lenaerts, Annet Storm, Lies Schoonaert, Antina de Boer, Philip Van Damme, Ludo Van Den Bosch, Wim Robberecht, Robin Lemmens
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
EphA4 is a receptor of the Eph-ephrin system, which plays an important role in axon guidance during development. Previously, we identified EphA4 as a genetic modifier of amyotrophic lateral sclerosis (ALS) in both zebrafish and rodent models, via mod
Externí odkaz:
https://doaj.org/article/c4eef57802cd4256aec80742c79d45db
Autor:
Elke Rammant, Ann Van Hecke, Jelle Van Cauwenberg, Karel Decaestecker, Lindsay Poppe, Beth Russel, Renée Bultijnck, Maarten Albersen, Sofie Verhaeghe, Mieke Van Hemelrijck, Roos Colman, Benedicte Deforche, Valérie Fonteyne
Publikováno v:
Bladder Cancer. 8:395-404
BACKGROUND: Emerging evidence shows a positive impact of physical activity (PA) on health-related quality of life (HRQoL) in cancer patients. However, longitudinal evidence on PA and HRQoL in patients with bladder cancer (BC) undergoing radical cyste
Autor:
Maricel Gomez-Soler, Lindsay Poppe, Robin Lemmens, Elena B. Pasquale, Silke Smolders, Antina de Boer, Wim Robberecht, Annet Storm, Laura Rué
Publikováno v:
Human Molecular Genetics
Worldwide, stroke is the main cause of long-term adult disability. After the initial insult, most patients undergo a subacute period with intense plasticity and rapid functional improvements. This period is followed by a chronic phase where recovery
Autor:
Charlien Berghen, Sylvie Rottey, Karel Decaestecker, Valérie Fonteyne, Gert De Meerleer, Pieter De Visschere, Charles Van Praet, Maarten Albersen, Piet Ost, Daan De Maeseneer, Flor Verghote, Lindsay Poppe, Piet Dirix, Geert Villeirs, Sofie Verbeke, Kathia De Man
Publikováno v:
BMC CANCER
BMC Cancer, Vol 21, Iss 1, Pp 1-7 (2021)
BMC Cancer
BMC Cancer, Vol 21, Iss 1, Pp 1-7 (2021)
BMC Cancer
Background The outcome of patients with muscle-invasive bladder cancer (MIBC) remains poor, despite aggressive treatments. Inadequate primary staging, classically performed by computed tomography (CT)-imaging, could lead to inappropriate treatment an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bdd27a63fb936b9a3c823f48d29cbce
https://lirias.kuleuven.be/handle/20.500.12942/686958
https://lirias.kuleuven.be/handle/20.500.12942/686958
Autor:
Mieke Timmers, Silke Smolders, Bart De Strooper, Annette Lenaerts, Annet Storm, Laura Rué, Wim Robberecht, Robin Lemmens, Lindsay Poppe, Philip Van Damme, Ludo Van Den Bosch, Gilles Courtand, Antina de Boer, Zsuzsanna Callaerts-Vegh, Rudi D'Hooge
Publikováno v:
Alzheimer's Research & Therapy
Alzheimer’s Research & Therapy, Vol 11, Iss 1, Pp 1-13 (2019)
Alzheimer’s Research & Therapy, Vol 11, Iss 1, Pp 1-13 (2019)
Background EphA4 is a receptor of the ephrin system regulating spine morphology and plasticity in the brain. These processes are pivotal in the pathophysiology of Alzheimer’s disease (AD), characterized by synapse dysfunction and loss, and the prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::011f9c03e5504e84a1847641f50473c1
https://lirias.kuleuven.be/handle/123456789/646258
https://lirias.kuleuven.be/handle/123456789/646258
Autor:
Antina de Boer, Annette Lenaerts, Silke Smolders, Philip Van Damme, Laura Rué, Ludo Van Den Bosch, Robin Lemmens, Mieke Timmers, Lindsay Poppe, Wim Robberecht
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific Reports
Scientific Reports
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that affects motor neurons resulting in severe neurological symptoms. Previous findings of our lab suggested that the axonal guidance tyrosine-kinase receptor EphA4 is an ALS disease-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d775e91e704e3d90c7a5c6672e33459
https://lirias.kuleuven.be/handle/123456789/644294
https://lirias.kuleuven.be/handle/123456789/644294
Autor:
Albert C. Ludolph, Jochen H. Weishaupt, Philip Van Damme, Annette Lenaerts, Wim Robberecht, Jasmijn van der Vos, Silke Smolders, Laura Rué, Patrick Oeckl, Ludo Van Den Bosch, Antina de Boer, Lindsay Poppe, Mieke Timmers, Robin Lemmens, Markus Otto
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-15 (2019)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that affects motor neurons in the brainstem, spinal cord and motor cortex. ALS is characterized by genetic and clinical heterogeneity, suggesting the existence of genetic factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3999b4f7642b8bc4a85ad649a1c41343
https://lirias.kuleuven.be/handle/123456789/644713
https://lirias.kuleuven.be/handle/123456789/644713