Zobrazeno 1 - 9
of 9
pro vyhledávání: '"E H Niks"'
Autor:
M T Hooijmans, N Doorenweerd, C Baligand, J J G M Verschuuren, I Ronen, E H Niks, A G Webb, H E Kan
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0182086 (2017)
To assess the changes in phosphodiester (PDE)-levels, detected by 31P magnetic resonance spectroscopy (MRS), over 24-months to determine the potential of PDE as marker for muscle tissue changes in Duchenne Muscular Dystrophy (DMD) patients.Spatially
Externí odkaz:
https://doaj.org/article/ad08d6eda20f466ab91105c46a92fd2c
Autor:
Z. Koeks, A. A. Janson, C. Beekman, M. Signorelli, H. A. van Duyvenvoorde, J. C. van den Bergen, M. T. Hooijmans, I. Alleman, I. M. Hegeman, J. J. G. M. Verschuuren, J. C. v. Deutekom, P. Spitali, N. A. Datson, E. H. Niks
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Becker muscular dystrophy (BMD) is the milder allelic variant of Duchenne muscular dystrophy, with higher dystrophin levels. To anticipate on results of interventions targeting dystrophin expression it is important to know the natural variat
Externí odkaz:
https://doaj.org/article/a23260bb186d44e7bd39cda7039c48a5
Autor:
T Gegenava, N Van De Velde, Z Koeks, P Spitali, J J G M Verschuuren, V Delgado, J Bax, E H Niks, N Ajmone-Marsan
Publikováno v:
European Heart Journal. 43
Background Becker muscular dystrophy (BMD) is frequently characterized by myocardial involvement1 but little is known about the prevalence of left ventricular (LV) diastolic dysfunction (DD) in these patients, particularly when using more recently pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b13d9a845a62d46a44df788a77a9f907
https://doi.org/10.1093/eurheartj/ehac544.2624
https://doi.org/10.1093/eurheartj/ehac544.2624
Autor:
J.C. van den Bergen, Anneke A.M. Janson, Zaïda Koeks, Jan J.G.M. Verschuuren, Melissa T. Hooijmans, Pietro Spitali, Iris Alleman, C. Beekman, E. H. Niks, N. A. Datson, Mirko Signorelli, H.A. van Duyvenvoorde, I. M. Hegeman, J. C. v. Deutekom
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports, 11(1). NATURE RESEARCH
Scientific reports, 11(1):5952. Nature Publishing Group
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports, 11(1). NATURE RESEARCH
Scientific reports, 11(1):5952. Nature Publishing Group
Becker muscular dystrophy (BMD) is the milder allelic variant of Duchenne muscular dystrophy, with higher dystrophin levels. To anticipate on results of interventions targeting dystrophin expression it is important to know the natural variation of dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6f2abccccac3da78faff9950f627c61
https://pubmed.ncbi.nlm.nih.gov/33723284
https://pubmed.ncbi.nlm.nih.gov/33723284
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 161
Every child with a life-limiting or threatening illness, and his or her family, has a right to palliative care. Palliative care is not limited to end-of-life care, but starts from the moment of diagnosis and is independent of whether there are curati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c042f632d3c09b15bccc690c37f99e61
https://pubmed.ncbi.nlm.nih.gov/28294926
https://pubmed.ncbi.nlm.nih.gov/28294926
Autor:
J C, van den Bergen, H B, Ginjaar, A J, van Essen, R, Pangalila, I J M, de Groot, P J, Wijkstra, M P, Zijnen, N A M, Cobben, M J, Kampelmacher, B H A, Wokke, I F M, de Coo, J M, Fock, A M C, Horemans, M, van Tol, E, Vroom, M E B, Rijlaarsdam, C S M, Straathof, E H, Niks, J J G M, Verschuuren
Publikováno v:
Journal of neuromuscular diseases. 1(1)
Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy is currently available, but in recent decades standards of care have improved. These improvements include the use of corticosteroids and mechanical ventilation.To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ac9903fe763610bd21edc9dbec33ead
https://pubmed.ncbi.nlm.nih.gov/27858664
https://pubmed.ncbi.nlm.nih.gov/27858664
Publikováno v:
NMR in biomedicine. 30(1)
Quantitative MRI and MRS are increasingly important as non-invasive outcome measures in therapy development for Duchenne muscular dystrophy (DMD). Many studies have focussed on individual measures such as fat fraction and metabolite levels in relatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0cb39d6e24123a5bd61a46eb08dd6f90
https://pubmed.ncbi.nlm.nih.gov/27859827
https://pubmed.ncbi.nlm.nih.gov/27859827
Autor:
M T, Hooijmans, B M, Damon, M, Froeling, M J, Versluis, J, Burakiewicz, J J G M, Verschuuren, E H, Niks, A G, Webb, H E, Kan
Publikováno v:
NMR in biomedicine. 28(11)
Diffusion tensor imaging (DTI) is a popular method to assess differences in fiber organization in diseased and healthy muscle tissue. Previous work has shown that muscle DTI measurements depend on signal-to-noise ratio (SNR), %fat, and tissue T2. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52c52305a0744cc8209a4e24c81a350e
https://pubmed.ncbi.nlm.nih.gov/26449628
https://pubmed.ncbi.nlm.nih.gov/26449628
Autor:
M. Tol van der, Imelda J. M. de Groot, H.B. Ginjaar, Elizabeth Vroom, Jan J.G.M. Verschuuren, Z. Koeks, N. Wolf, Chiara S. M. Straathof, E. H. Niks, J.G.M. Hendriksen, C. G. Faber, Annemarie Fock, Robert F. Pangalila, J.C. Bergen van den, A. M. C. Horemans, A.M. Aastsma-Rus, Irenaeus F.M. de Coo, A. Kooi van der
Publikováno v:
Neuromuscular Disorders. 23:775-776
Dystrophinopathy patient registries are very useful for improvement of standard care and planning of clinical trials. The Dutch Dystrophinopathy Database contains information of Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::523465d2c3a84c2a9e79a110cae40329
https://doi.org/10.1016/j.nmd.2013.06.489
https://doi.org/10.1016/j.nmd.2013.06.489