Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Camiel A Wijngaarde"'
Autor:
Renske I Wadman, Marloes Stam, Marc D Jansen, Yana van der Weegen, Camiel A Wijngaarde, Oliver Harschnitz, Peter Sodaar, Kees P J Braun, Dennis Dooijes, Henny H Lemmink, Leonard H van den Berg, W Ludo van der Pol
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0167087 (2016)
Clinical trials to test safety and efficacy of drugs for patients with spinal muscular atrophy (SMA) are currently underway. Biomarkers that document treatment-induced effects are needed because disease progression in childhood forms of SMA is slow a
Externí odkaz:
https://doaj.org/article/e99f54abe7b64ae79f3fd84102bb4fb4
Autor:
Esther S. Veldhoen, Camiel A. Wijngaarde, Ruben P. A. van Eijk, Fay-Lynn Asselman, Negina Seddiqi, Louise A. M. Otto, Marloes Stam, Inge Cuppen, Renske I. Wadman, Roelie M. Wösten van Asperen, Erik H. J. Hulzebos, Laura P. Verweij van den Oudenrijn, Bart Bartels, Jasmijn Boezer, M. Gaytant, Cornelis K. van der Ent, W. Ludo van der Pol
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Progressive lung function decline, resulting in respiratory failure, is an important complication of spinal muscular atrophy (SMA). The ability to predict the need for mechanical ventilation is important. We assessed longitudinal
Externí odkaz:
https://doaj.org/article/28db6b5241394763846f3233ab257034
Autor:
Bart Bartels, Janke F. de Groot, Laura E. Habets, Camiel A. Wijngaarde, Wendy Vink, Marloes Stam, Fay-Lynn Asselman, Ruben P. A. van Eijk, W. Ludo van der Pol
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background To determine construct validity and test-retest reliability of Endurance Shuttle Tests as outcome measures for fatigability of remaining motor functions in children and adults with Spinal Muscular Atrophy (SMA) across the severity
Externí odkaz:
https://doaj.org/article/eac1a0ba8eba4fefb1c4f3a6043dbd46
Autor:
Marloes Stam, Camiel A Wijngaarde, Bart Bartels, Fay-Lynn Asselman, Louise A M Otto, Laura E Habets, Ruben P A van Eijk, Bas M Middelkoop, H Stephan Goedee, Janke F de Groot, Kit C B Roes, Marja A G C Schoenmakers, Edward E S Nieuwenhuis, Inge Cuppen, Leonard H van den Berg, Renske I Wadman, W Ludo van der Pol
Publikováno v:
Brain Communications, 5
Brain Communications, 5, 1
Brain Communications, 5, 1
Hereditary proximal spinal muscular atrophy causes weakness and increased fatigability of repetitive motor functions. The neuromuscular junction is anatomically and functionally abnormal in patients with spinal muscular atrophy. Pharmacological impro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21143b70317859320feacf01880264ea
http://hdl.handle.net/2066/289329
http://hdl.handle.net/2066/289329
Autor:
Esther S. Veldhoen, Camiel A. Wijngaarde, Ruben P. A. van Eijk, Fay-Lynn Asselman, Negina Seddiqi, Louise A. M. Otto, Marloes Stam, Inge Cuppen, Renske I. Wadman, Roelie M. Wösten van Asperen, Erik H. J. Hulzebos, Laura P. Verweij van den Oudenrijn, Bart Bartels, Jasmijn Boezer, M. Gaytant, Cornelis K. van der Ent, W. Ludo van der Pol
Background Progressive lung function decline, resulting in respiratory failure, is an important complication of spinal muscular atrophy (SMA). The ability to predict the need for mechanical ventilation is important. We assessed longitudinal patterns
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2414b9c1832dcc46233ff19e7306967
https://doi.org/10.21203/rs.3.rs-2083566/v1
https://doi.org/10.21203/rs.3.rs-2083566/v1
Autor:
Esther S. Veldhoen, Johan H. Roos, Rolien Bekkema, Ludo W. van der Pol, Marcel H. B. Tinnevelt, Laura P. Verweij‐van den Oudenrijn, Roelie M. Wösten‐van Asperen, Erik H. J. Hulzebos, Camiel A. Wijngaarde, Cornelis K. van der Ent
Publikováno v:
Pediatric pulmonology. 57(7)
Spirometry plays an important role in the assessment of possible respiratory failure in children with neuromuscular diseases (NMDs). However, obtaining reliable spirometry results is a major challenge. We studied the relation between oscillometry and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab622e5ae833f81d45af4a192c04dc34
https://pubmed.ncbi.nlm.nih.gov/35441830
https://pubmed.ncbi.nlm.nih.gov/35441830
Autor:
H. Stephan Goedee, Renske I. Wadman, Fay-Lynn Asselman, Boudewijn T.H.M. Sleutjes, Inge Cuppen, Leonard H. van den Berg, Louise A.M. Otto, Camiel A. Wijngaarde, W. Ludo van der Pol
Publikováno v:
Clinical Neurophysiology. 131:1280-1286
Objective To assess motor unit (MU) changes in patients with spinal muscular atrophy (SMA) using compound muscle action potential (CMAP) scans. Methods We performed CMAP scan recordings in median nerves of 24 treatment-naive patients (median age 39;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91e1689d27eeac5ab822ea01e748adb0
https://doi.org/10.1016/j.clinph.2020.01.018
https://doi.org/10.1016/j.clinph.2020.01.018
Autor:
Marloes Stam, Louise A.M. Otto, Erik H. J. Hulzebos, Cornelis K. van der Ent, Renske I. Wadman, Roelie M. Wösten-van Asperen, Inge Cuppen, Camiel A. Wijngaarde, Laura P. Verweij-van den Oudenrijn, Bart Bartels, Ruben P A van Eijk, Fay-Lynn Asselman, W. Ludo van der Pol, Esther S. Veldhoen, Leonard H. van den Berg
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Respiratory muscle weakness is an important feature of spinal muscular atrophy (SMA). Progressive lung function decline is the most important cause of mortality and morbidity in patients. The natural history of lung function in SMA has, ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fab2f2390c6dd720e0c6d42ad3fac47
http://link.springer.com/article/10.1186/s13023-020-01367-y
http://link.springer.com/article/10.1186/s13023-020-01367-y
Autor:
Inge Cuppen, W. Ludo van der Pol, Renske I. Wadman, Leonard H. van den Berg, Marloes Stam, Ruben P A van Eijk, Camiel A. Wijngaarde, Louise A.M. Otto, Esther S. Veldhoen
Publikováno v:
Neurology. 94:e1634-e1644
ObjectiveTo investigate probabilities of survival and its surrogate, that is, mechanical ventilation, in patients with spinal muscular atrophy (SMA).MethodsWe studied survival in a population-based cohort on clinical prevalence of genetically confirm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ac70e2034345899f32f4af454f73d9c
https://doi.org/10.1212/wnl.0000000000009248
https://doi.org/10.1212/wnl.0000000000009248
Autor:
Fay Lynn Asselman, Inge Cuppen, Esther S. Veldhoen, Roelie W Wosten-van Asperen, Michael A. Gaytant, Camiel A. Wijngaarde, Louise A.M. Otto, Ruben P A van Eijk, Renske I. Wadman, Erik H. J. Hulzebos, Feline E.V. Scheijmans, W. Ludo van der Pol, Cornelis K. van der Ent, Bart Bartels, Laura P. Verweij-van den Oudenrijn, Marloes Stam
Publikováno v:
Orphanet Journal of Rare Diseases. 17
Background Respiratory complications are the most important cause of morbidity and mortality in spinal muscular atrophy (SMA). Respiratory muscle weakness results in impaired cough, recurrent respiratory tract infections and eventually can cause resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dab90a8f6b70795e901cd102f7b5ba32
https://doi.org/10.1186/s13023-022-02227-7
https://doi.org/10.1186/s13023-022-02227-7