Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Stijn, Stroobants"'
Autor:
Stijn Stroobants, Kim Dockx, Hans Scheers, Vere Borra, Niels De Brier, Sarah Verlinden, Karen Lauwers, Philippe Vandekerckhove, Emmy De Buck
Publikováno v:
International Journal of First Aid Education, Vol 6, Iss 1, Pp 37–60-37–60 (2023)
Background: Family and friends are particularly well placed to recognize early signs of mental health problems, provide initial support, and refer to professional help if needed. This project aimed to develop evidence-based guidance materials for lay
Externí odkaz:
https://doaj.org/article/7d3ffbaad04a421485d0ef7349fa06ed
Autor:
Hans Scheers, Hans Van Remoortel, Karen Lauwers, Johan Gillebeert, Stijn Stroobants, Pascal Vranckx, Emmy De Buck, Philippe Vandekerckhove
Publikováno v:
BMC Public Health, Vol 22, Iss 1, Pp 1-17 (2022)
Abstract Background Every year, volunteers of the Belgian Red Cross provide onsite medical care at more than 8000 mass gathering events and other manifestations. Today standardized planning tools for optimal preventive medical resource use during the
Externí odkaz:
https://doaj.org/article/d26486ef60c0455d828be2ba34407e72
Autor:
Lien Beckers, Ivana Geric, Stijn Stroobants, Sander Beel, Philip Van Damme, Rudi D’Hooge, Myriam Baes
Publikováno v:
Journal of Neuroinflammation, Vol 16, Iss 1, Pp 1-15 (2019)
Abstract Background Microglia play a central role in most neurological disorders, but the impact of microgliosis on brain environment and clinical functions is not fully understood. Mice lacking multifunctional protein-2 (MFP2), a pivotal enzyme in p
Externí odkaz:
https://doaj.org/article/cc0f797511704c9d955ebba5c9fc01a8
Autor:
Patrick Lüningschrör, Georg Werner, Stijn Stroobants, Soichiro Kakuta, Benjamin Dombert, Daniela Sinske, Renate Wanner, Renate Lüllmann-Rauch, Benedikt Wefers, Wolfgang Wurst, Rudi D’Hooge, Yasuo Uchiyama, Michael Sendtner, Christian Haass, Paul Saftig, Bernd Knöll, Anja Capell, Markus Damme
Publikováno v:
Cell Reports, Vol 30, Iss 10, Pp 3506-3519.e6 (2020)
Summary: Genetic variations in TMEM106B, coding for a lysosomal membrane protein, affect frontotemporal lobar degeneration (FTLD) in GRN- (coding for progranulin) and C9orf72-expansion carriers and might play a role in aging. To determine the physiol
Externí odkaz:
https://doaj.org/article/6a9f42b14fca4fb8a5526634d9334b2c
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227034 (2020)
Infant-parent attachment is highly selective and continues beyond essential care in primates, most prominently in humans, and the quality of this attachment crucially determines cognitive and emotional development of the infant. Altricial rodent spec
Externí odkaz:
https://doaj.org/article/68cc930d73e84eeaabd6acc1f0d36040
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0244052 (2020)
IntroductionThe novel Coronavirus Disease (COVID-19) outbreak currently puts health care workers at high risk of both physical and mental health problems. This study aimed to identify the risk and protective factors for mental health outcomes in heal
Externí odkaz:
https://doaj.org/article/a95c0f5337e841b4b9706209c322e0ea
Publikováno v:
Frontiers in Aging Neuroscience, Vol 11 (2019)
Neurocognitive disorders, among which Alzheimer’s disease (AD), have become one of the major causes of death in developed countries. No effective disease-modifying therapy is available, possibly because current treatments are administered too late
Externí odkaz:
https://doaj.org/article/4f5be2d041a64410be58cf8a66ef0352
Autor:
Stijn Stroobants, Markus Damme, Ann Van der Jeugd, Ben Vermaercke, Claes Andersson, Jens Fogh, Paul Saftig, Judith Blanz, Rudi D'Hooge
Publikováno v:
Neurobiology of Disease, Vol 106, Iss , Pp 255-268 (2017)
Alpha-mannosidosis is a glycoproteinosis caused by deficiency of lysosomal acid alpha-mannosidase (LAMAN), which markedly affects neurons of the central nervous system (CNS), and causes pathognomonic intellectual dysfunction in the clinical condition
Externí odkaz:
https://doaj.org/article/69731922a1654397bfd10619a9c92c07
Autor:
Heike Wolf, Markus Damme, Stijn Stroobants, Rudi D'Hooge, Hans Christian Beck, Irm Hermans-Borgmeyer, Renate Lüllmann-Rauch, Thomas Dierks, Torben Lübke
Publikováno v:
Disease Models & Mechanisms, Vol 9, Iss 9, Pp 1015-1028 (2016)
Fucosidosis is a rare lysosomal storage disorder caused by the inherited deficiency of the lysosomal hydrolase α-L-fucosidase, which leads to an impaired degradation of fucosylated glycoconjugates. Here, we report the generation of a fucosidosis mou
Externí odkaz:
https://doaj.org/article/138a1d71f754489d931af1f83c6469a3
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 12 (2018)
It is becoming evident that microglia, the resident immune cells of the central nervous system (CNS), are active contributors in neurological disorders. Nevertheless, the impact of microgliosis on neuropathology, behavior and clinical decline in neur
Externí odkaz:
https://doaj.org/article/da1818498e2b4723a1f0c356aa7a652e