Zobrazeno 1 - 10
of 72
pro vyhledávání: '"H. Sonneveld"'
Autor:
Laura J. H. Sonneveld, Joyce A. M. Emons, Nicolette J. T. Arends, Lonneke J. Landzaat, Sharon Veenbergen, Marco W. J. Schreurs
Publikováno v:
Clinical and Molecular Allergy, Vol 20, Iss 1, Pp 1-7 (2022)
Abstract ALEX multiplex array is a relatively new multiplex allergy test which analyses more than 120 allergen extracts and 170 molecular components. ISAC is the most used and studied multiplex array to date, offering 112 molecular components. In ten
Externí odkaz:
https://doaj.org/article/82a6a3536f1a416aa5f6831fd7d62a2f
Autor:
Lonneke J. Landzaat, Joyce A. M. Emons, Laura J. H. Sonneveld, Marco W. J. Schreurs, Nicolette J. T. Arends
Publikováno v:
Frontiers in Allergy, Vol 4 (2023)
BackgroundAllergic rhinitis is a common respiratory disease in children and sensitization to inhalant allergens plays a significant role in its development. However, limited knowledge exists regarding sensitization profiles of inhalant allergen compo
Externí odkaz:
https://doaj.org/article/8cc8f7bf1c2e4d37b1f03917a33aa54e
Autor:
Johanna G. Douma, Karin M. Volkers, Gwenda Engels, Marieke H. Sonneveld, Richard H.M. Goossens, Erik J.A. Scherder
Publikováno v:
BMC Geriatrics, Vol 17, Iss 1, Pp 1-10 (2017)
Abstract Background Despite the detrimental effects of physical inactivity for older adults, especially aged residents of residential care settings may spend much time in inactive behavior. This may be partly due to their poorer physical condition; h
Externí odkaz:
https://doaj.org/article/03550c43500040d78e4f9902920cf052
Autor:
Janine E van Loon, Michelle A H Sonneveld, Stephan F E Praet, Moniek P M de Maat, Frank W G Leebeek
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91687 (2014)
Physical stress triggers the endothelium to release von Willebrand Factor (VWF) from the Weibel Palade bodies. Since VWF is a risk factor for arterial thrombosis, it is of great interest to discover determinants of VWF response to physical stress. We
Externí odkaz:
https://doaj.org/article/f087811e3fc341fe990534ec54d026ae
This Policy Review presents the International Myeloma Working Group's clinical practice recommendations for the treatment of relapsed and refractory multiple myeloma. Based on the results of phase 2 and phase 3 trials, these recommendations are propo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d3015bd5fa13fd6d90fb842a28dba1cb
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3102710
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3102710
Autor:
Bierlaagh, M., Lefferts, J., Kroes, S., Nieuwenhuijze, N., van Kooten, H. Sonneveld, Muilwijk, D., Niemoller, P., Verburg, T., van der Ent, K., Beekman, J.
Publikováno v:
In Journal of Cystic Fibrosis October 2023 22 Supplement 3:S161-S162
For patients with newly diagnosed multiple myeloma (NDMM) who are transplant ineligible, bortezomib-melphalan-prednisone (VMP) demonstrated superior efficacy based on the VISTA trial. In subsequent trials, twice-weekly bortezomib was limited to the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e3adfc4a15c11276a2ca311380f0bdf8
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078530
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078530
Deletions of chromosome 17p (del17p) that span the TP53 gene are associated with poor outcome in multiple myeloma (MM), but the prognostic value of del17p cancer clonal fraction (CCF) remains unclear. We applied uniform cytogenetic assessments in a l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d36368ae36d6e80e96732ea625096df6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3000466
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3000466
Background: The novel proteasome inhibitor carfilzomib alone or in combination with other agents is already one of the standard therapies for relapsed and/or refractory multiple myeloma (MM) patients and produces impressive response rates in newly di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::bf39972377b71e040733c5d992635533
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3105895
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3105895
Publikováno v:
Journal of clinical endocrinology and metabolism, 100(11), 3963-3966. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 100(11), 3963-3966
Journal of Clinical Endocrinology and Metabolism, 100(11), 3963-3966
Several patients with Beckwith-Wiedemann Syndrome (BWS) with multiple imprinting defects found by genetic analysis have been described. However, only two cases have been described with both genetic and clinical signs and symptoms of multiple diseases