Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Camiel Verhamme"'
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
Autor:
Corianne A J M de Borgie, WIM I M VERHAGEN, Diederik van de Beek, Esther Verstraete, Korné Jellema, Rob M A de Bie, Camiel Verhamme, Wijnand A C Palmbergen, Tim W H Alleman, Geert J F Brekelmans, Godard C W de Ruiter, Rob de Haan, Roy Beekman
Publikováno v:
BMJ Open, Vol 12, Iss 4 (2022)
Introduction Carpal tunnel syndrome (CTS) is the most common peripheral neuropathy. The optimal treatment strategy is still unknown. The objective of the Dutch Injection versus Surgery TRIal in patients with CTS (DISTRICTS) is to investigate if initi
Externí odkaz:
https://doaj.org/article/442ee47f13864a65b8aedc7af0e52914
Autor:
Sander Oorschot, Merel A. Brehm, Annerieke C. van Groenestijn, Fieke S. Koopman, Camiel Verhamme, Filip Eftimov, Judith G. M. Jelsma, Harald T. Jorstad, Frans Nollet, Eric L. Voorn
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-10 (2020)
Abstract Background In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue and pain may limit physical activity. Inactivity leads to reduced physical fitness, which further complicates daily life functioning. Due to in
Externí odkaz:
https://doaj.org/article/ee64e892d3004b3fb215e07323099659
Autor:
Esther Witteveen, Juultje Sommers, Luuk Wieske, Jonne Doorduin, Nens van Alfen, Marcus J. Schultz, Ivo N. van Schaik, Janneke Horn, Camiel Verhamme
Publikováno v:
Annals of Intensive Care, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract Background Neuromuscular ultrasound is a noninvasive investigation, which can be easily performed at the bedside on the ICU. A reduction in muscle thickness and increase in echo intensity over time have been described in ICU patients, but th
Externí odkaz:
https://doaj.org/article/2ebee9c5f71c4e21af1f440d1ab9ba25
Autor:
Jos Oudeman, Camiel Verhamme, Maurits P Engbersen, Mattan W A Caan, Mario Maas, Martijn Froeling, Aart J Nederveen, Gustav J Strijkers
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0196975 (2018)
Diffusion Tensor MRI (DT-MRI) is a promising tool for the evaluation of brachial plexus pathology. Therefore, we introduce and evaluate a fast DT-MRI protocol (8min33s scanning with 5-10 min postprocessing time) for the brachial plexus.Thirty healthy
Externí odkaz:
https://doaj.org/article/d6a2c93c816c437d8631725dc03c481b
Autor:
Luuk Wieske, Esther Witteveen, Camiel Verhamme, Daniela S Dettling-Ihnenfeldt, Marike van der Schaaf, Marcus J Schultz, Ivo N van Schaik, Janneke Horn
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e111259 (2014)
An early diagnosis of Intensive Care Unit-acquired weakness (ICU-AW) using muscle strength assessment is not possible in most critically ill patients. We hypothesized that development of ICU-AW can be predicted reliably two days after ICU admission,
Externí odkaz:
https://doaj.org/article/beb40d163e87482683ea523da2adbcb1
Autor:
Samuel Arends, Judith Drenthen, Peter van den Bergh, Hessel Franssen, Robert D.M. Hadden, Badrul Islam, Satoshi Kuwabara, Ricardo C. Reisin, Nortina Shahrizaila, Hiroshi Amino, Giovanni Antonini, Shahram Attarian, Claudia Balducci, Fabio Barroso, Tulio Bertorini, Davide Binda, Thomas H. Brannagan, Jan Buermann, Carlos Casasnovas, Guido Cavaletti, Chi-Chao Chao, Mazen M. Dimachkie, Ernesto A. Fulgenzi, Giuliana Galassi, Gerardo Gutiérrez Gutiérrez, Thomas Harbo, Hans-Peter Hartung, Sung-Tsang Hsieh, Lynette Kiers, Helmar C. Lehmann, Fiore Manganelli, Girolama A. Marfia, Giorgia Mataluni, Julio Pardo, Yann Péréon, Yusuf A. Rajabally, Lucio Santoro, Yukari Sekiguchi, Beth Stein, Mark Stettner, Antonino Uncini, Christine Verboon, Camiel Verhamme, Michal Vytopil, Waqar Waheed, Min Wang, Sasha Zivkovic, Bart C. Jacobs, David R. Cornblath, J.M. Addington, S. Ajroud-Driss, H. Andersen, G. Antonini, S. Attarian, U.A. Badrising, G. Balloy, F.A. Barroso, K. Bateman, I.R. Bella, L. Benedetti, P. van den Bergh, T.E. Bertorini, R. Bhavaraju-Sanka, M. Bianco, T.H. Brannagan, C. Briani, null Buerrmann, M. Busby, S. Butterworth, C. Casasnovas, G. Cavaletti, C.C. Chao, G. Chavada, S. Chen, K.G. Claeys, M.E. Conti, D.R. Cornblath, J.S. Cosgrove, M.C. Dalakas, P. van Damme, E. Dardiotis, A. Davidson, M.A. Derejko, G.W. van Dijk, M.M. Dimachkie, P.A. van Doorn, C. Dornonville de la Cour, A. Echaniz-Laguna, F. Eftimov, C.G. Faber, R. Fazio, T.E. Feasby, C. Fokke, T. Fujioka, E.A. Fulgenzi, G. Galassi, T. Garcia-Sobrino, M.P.J. Garssen, C.J. Gijsbers, J.M. Gilchrist, H.J. Gilhuis, J.M. Goldstein, K.C. Gorson, N.A. Goyal, V. Granit, S.T.E. Grisanti, null Gutiérrez-Gutiérrez, L. Gutmann, R.D.M. Hadden, T. Harbo, H.P. Hartung, J.V. Holbech, J.K.L. Holt, S.T. Hsieh, M. Htut, R.A.C. Hughes, I. Illa, B. Islam, Z. Islam, B.C. Jacobs, J. Fehmi, K. Jellema, I. Jerico Pascual, K. Kaida, S. Karafiath, H.D. Katzberg, M.A. Khoshnoodi, L. Kiers, K. Kimpinski, R.P. Kleyweg, N. Kokubun, N.A. Kolb, R. van Koningsveld, A.J. van der Kooi, J.C.H.M. Kramers, K. Kuitwaard, S. Kusunoki, S. Kuwabara, J.Y. Kwan, S.S. Ladha, L. Landschoff Lassen, V. Lawson, H.C. Lehmann, E. Lee Pan, M.P.T. Lunn, H. Manji, G.A. Marfia, C. Márquez Infante, L. Martin-Aguilar, E. Martinez Hernandez, G. Mataluni, M. Mattiazi, C.J. McDermott, G.D. Meekins, J.A.L. Miller, Q.D. Mohammad, M.S. Monges, G. Moris de la Tassa, C. Nascimbene, F.J. Navacerrada-Barrero, E. Nobile-Orazio, R.J. Nowak, P.J. Orizaola, M. Osei-Bonsu, A.M. Pardal, J. Pardo, R.M. Pascuzzi, Y. Péréon, M.T. Pulley, L. Querol, S.W. Reddel, T. van der Ree, R.C. Reisin, S. Rinaldi, R.C. Roberts, I. Rojas-Marcos, null Rudnicki, G.M. Sachs, J.P.A. Samijn, L. Santoro, A. Schenone, M.J. Sedano Tous, N. Shahrizaila, K.A. Sheikh, N.J. Silvestri, S.H. Sindrup, C.L. Sommer, B. Stein, Y. Song, A.M. Stino, H. Tankisi, M.R. Tannemaat, P. Twydell, P.V. Vélez-Santamaria, J.D. Varrato, F.H. Vermeij, L.H. Visser, M.V. Vytopil, W. Waheed, C. Walgaard, Y.Z. Wang, H.J. Willison, P.W. Wirtz, Y. Yamagishi, L. Zhou, S.A. Zivkovic
Publikováno v:
Clinical Neurophysiology, 138, 231-240. ELSEVIER IRELAND LTD
Clinical neurophysiology, 138, 231-240. Elsevier Ireland Ltd
Dipòsit Digital de la UB
Universidad de Barcelona
Arends, S, Drenthen, J, van den Bergh, P, Franssen, H, Hadden, R D M, Islam, B, Kuwabara, S, Reisin, R C, Shahrizaila, N, Amino, H, Antonini, G, Attarian, S, Balducci, C, Barroso, F, Bertorini, T, Binda, D, Brannagan, T H, Buermann, J, Casasnovas, C, Cavaletti, G, Chao, C C, Dimachkie, M M, Fulgenzi, E A, Galassi, G, Gutiérrez Gutiérrez, G, Harbo, T, Hartung, H P, Hsieh, S T, Kiers, L, Lehmann, H C, Manganelli, F, Marfia, G A, Mataluni, G, Pardo, J, Péréon, Y, Rajabally, Y A, Santoro, L, Sekiguchi, Y, Stein, B & the IGOS consortium 2022, ' Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study : Differences in methods and reference values ', Clinical Neurophysiology, vol. 138, pp. 231-240 . https://doi.org/10.1016/j.clinph.2021.12.014
Clinical Neurophysiology, 138, 231-240. Elsevier Ireland Ltd
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, Vol. 138, no.1, p. 231-240 (2022)
Clinical neurophysiology, 138, 231-240. Elsevier Ireland Ltd
Dipòsit Digital de la UB
Universidad de Barcelona
Arends, S, Drenthen, J, van den Bergh, P, Franssen, H, Hadden, R D M, Islam, B, Kuwabara, S, Reisin, R C, Shahrizaila, N, Amino, H, Antonini, G, Attarian, S, Balducci, C, Barroso, F, Bertorini, T, Binda, D, Brannagan, T H, Buermann, J, Casasnovas, C, Cavaletti, G, Chao, C C, Dimachkie, M M, Fulgenzi, E A, Galassi, G, Gutiérrez Gutiérrez, G, Harbo, T, Hartung, H P, Hsieh, S T, Kiers, L, Lehmann, H C, Manganelli, F, Marfia, G A, Mataluni, G, Pardo, J, Péréon, Y, Rajabally, Y A, Santoro, L, Sekiguchi, Y, Stein, B & the IGOS consortium 2022, ' Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study : Differences in methods and reference values ', Clinical Neurophysiology, vol. 138, pp. 231-240 . https://doi.org/10.1016/j.clinph.2021.12.014
Clinical Neurophysiology, 138, 231-240. Elsevier Ireland Ltd
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, Vol. 138, no.1, p. 231-240 (2022)
Objective: To describe the heterogeneity of electrodiagnostic (EDx) studies in Guillain-Barre syndrome (GBS) patients collected as part of the International GBS Outcome Study (IGOS). Methods: Prospectively collected clinical and EDx data were availab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45d27d06cfd93e03fcd6d104d087bdc1
https://doi.org/10.1016/j.clinph.2021.12.014
https://doi.org/10.1016/j.clinph.2021.12.014
Autor:
Anne W Walter, Johan Lim, Joost Raaphorst, Frank F Smithuis, J Michiel den Harder, Filip Eftimov, Wouter Potters, Christiaan G J Saris, Marianne de Visser, Ivo N van Schaik, Rob J de Haan, Anneke J van der Kooi, Camiel Verhamme
Publikováno v:
Rheumatology (Oxford, England), 62(1), 300-309. Oxford University Press
Walter, A W, Lim, J, Raaphorst, J, Smithuis, F F, den Harder, J M, Eftimov, F, Potters, W, Saris, C G J, de Visser, M, van Schaik, I N, de Haan, R J, van der Kooi, A J & Verhamme, C 2022, ' Ultrasound and MR muscle imaging in new onset idiopathic inflammatory myopathies at diagnosis and after treatment : a comparative pilot study ', Rheumatology (Oxford, England), vol. 62, no. 1, pp. 300-309 . https://doi.org/10.1093/rheumatology/keac263
Walter, A W, Lim, J, Raaphorst, J, Smithuis, F F, den Harder, J M, Eftimov, F, Potters, W, Saris, C G J, de Visser, M, van Schaik, I N, de Haan, R J, van der Kooi, A J & Verhamme, C 2022, ' Ultrasound and MR muscle imaging in new onset idiopathic inflammatory myopathies at diagnosis and after treatment : a comparative pilot study ', Rheumatology (Oxford, England), vol. 62, no. 1, pp. 300-309 . https://doi.org/10.1093/rheumatology/keac263
Objectives To prospectively compare ultrasound (US) and whole-body MRI for detection of muscle abnormalities compatible with idiopathic inflammatory myopathies (IIM). Methods Newly diagnosed IIM patients underwent US (14 muscles) and MRI (36 muscles)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a783b6c5151ee6774b752c7c9cd3809
https://pure.amc.nl/en/publications/ultrasound-and-mr-muscle-imaging-in-new-onset-idiopathic-inflammatory-myopathies-at-diagnosis-and-after-treatment(e2b4d1aa-59d2-4067-90cd-f83df4147f4e).html
https://pure.amc.nl/en/publications/ultrasound-and-mr-muscle-imaging-in-new-onset-idiopathic-inflammatory-myopathies-at-diagnosis-and-after-treatment(e2b4d1aa-59d2-4067-90cd-f83df4147f4e).html
