Zobrazeno 1 - 10
of 325
pro vyhledávání: '"Marianne, de Visser"'
Autor:
Antonio Atalaia, Dagmar Wandrei, Nawel Lalout, Rachel Thompson, Adrian Tassoni, Peter A. C. ’t Hoen, Dimitrios Athanasiou, Suzie-Ann Baker, Paraskevi Sakellariou, Georgios Paliouras, Carla D’Angelo, Rita Horvath, Michelangelo Mancuso, Nadine van der Beek, Cornelia Kornblum, Janbernd Kirschner, Davide Pareyson, Guillaume Bassez, Laura Blacas, Maxime Jacoupy, Catherine Eng, François Lamy, Jean-Philippe Plançon, Jana Haberlova, Esther Brusse, Janneke G. J. Hoeijmakers, Marianne de Visser, Kristl G. Claeys, Carmen Paradas, Antonio Toscano, Vincenzo Silani, Melinda Gyenge, Evy Reviers, Dalil Hamroun, Elisabeth Vroom, Mark D. Wilkinson, Hanns Lochmuller, Teresinha Evangelista
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-15 (2024)
Abstract Background The EURO-NMD Registry collects data from all neuromuscular patients seen at EURO-NMD's expert centres. In-kind contributions from three patient organisations have ensured that the registry is patient-centred, meaningful, and impac
Externí odkaz:
https://doaj.org/article/50645335f24240a3b4537c13391b28b5
This open access book analyzes how sound choices can be made in Dutch health care policies, and shows why they are necessary, urgent, and even inevitable. Analyzing the current functioning and funding of the Dutch health care system, this book shows
Autor:
Shahram Attarian, Peter Young, Thomas H. Brannagan, David Adams, Philip Van Damme, Florian P. Thomas, Carlos Casanovas, Jafar Kafaie, Céline Tard, Maggie C. Walter, Yann Péréon, David Walk, Amro Stino, Marianne de Visser, Camiel Verhamme, Anthony Amato, Gregory Carter, Laurent Magy, Jeffrey M. Statland, Kevin Felice
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/667ec559a27c41e486ae7d0fb0dca401
Autor:
Mario Maas, Anneke J van der Kooi, Joost Raaphorst, Ivo N van Schaik, Marianne de Visser, Johannes A Bogaards, Camiel Verhamme, Hannah A W Walter, Renske G Kamperman, Filip Eftimov, Sanne W Evers, Corianne de Borgie, Jantine C A Colen - de Koning
Publikováno v:
BMJ Open, Vol 13, Iss 7 (2023)
Introduction For idiopathic inflammatory myopathies (IIM) (‘myositis’) standard initial treatment is high-dosed glucocorticoids, which results in relatively slow improvement of muscle strength. Early immunosuppression or modulation by intensive t
Externí odkaz:
https://doaj.org/article/f36aa4640ead47e2953ceb3c54278423
Autor:
Shahram Attarian, Peter Young, Thomas H. Brannagan, David Adams, Philip Van Damme, Florian P. Thomas, Carlos Casanovas, Jafar Kafaie, Céline Tard, Maggie C. Walter, Yann Péréon, David Walk, Amro Stino, Marianne de Visser, Camiel Verhamme, Anthony Amato, Gregory Carter, Laurent Magy, Jeffrey M. Statland, Kevin Felice
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
Abstract Background Charcot–Marie–Tooth disease type 1A (CMT1A) is a rare, orphan, hereditary neuromuscular disorder with no cure and for which only symptomatic treatment is currently available. A previous phase 2 trial has shown preliminary evid
Externí odkaz:
https://doaj.org/article/cdd77817d00b47deb0f0fb315c44524e
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/b6309f814c8040c987c1f2bda4d6163b
Autor:
Rosanne Govaarts, Emma Beeldman, Matteo Fraschini, Alessandra Griffa, Marjolein M.A. Engels, Michael A. van Es, Jan H. Veldink, Leonard H. van den Berg, Anneke J. van der Kooi, Yolande A.L. Pijnenburg, Marianne de Visser, Cornelis J. Stam, Joost Raaphorst, Arjan Hillebrand
Publikováno v:
NeuroImage: Clinical, Vol 34, Iss , Pp 102965- (2022)
The objective of this study was to examine if patterns of resting-state brain activity and functional connectivity in cortical and subcortical regions in patients with early symptomatic amyotrophic lateral sclerosis (ALS) resemble those of behavioura
Externí odkaz:
https://doaj.org/article/46d3ddb87245498fbfe39480a5557fe9
Autor:
Elisabeth Kurpershoek, Marij A. Hillen, Niki M. Medendorp, Rob M. A. de Bie, Marianne de Visser, Joke M. Dijk
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Introduction: Advance care planning (ACP) is an iterative process of discussing the needs, wishes, and preferences of patients regarding disease-specific and end-of-life issues. There is ample evidence that ACP improves the quality of life and promot
Externí odkaz:
https://doaj.org/article/294b972f3039474c836284d7e25265a8
Autor:
Antje A. Seeber, A. Jeannette Pols, Albert Hijdra, Hepke F. Grupstra, Dick L. Willems, Marianne de Visser
Publikováno v:
BMC Palliative Care, Vol 18, Iss 1, Pp 1-10 (2019)
Abstract Background There is increasing awareness of the need for an integrated palliative care approach in chronic progressive neurological diseases. Advance care planning (ACP) is an integral part of this approach. As a systematically organized and
Externí odkaz:
https://doaj.org/article/3a3b849428b441539c471600de87ccad
Autor:
Marian A.J. Weterman, Marieke Bronk, Aldo Jongejan, Jessica E. Hoogendijk, Judith Krudde, Dyah Karjosukarso, Hans H. Goebel, Eleonora Aronica, G. Joost Jöbsis, Fred van Ruissen, Karin Y. van Spaendonck-Zwarts, Marianne de Visser, Frank Baas
Publikováno v:
Neuromuscular disorders. Elsevier Limited
Three families suspected of distal hereditary motor neuropathy underwent genetic screening with the aim to identify the molecular defect underlying the disease. The description of the identification reflects the shift in molecular diagnostics that wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd065e592f9a805e049c2aaf012ff810
https://doi.org/10.1016/j.nmd.2022.11.007
https://doi.org/10.1016/j.nmd.2022.11.007