Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Erik J van Helden"'
Autor:
Erik J van Helden, Otto S Hoekstra, Ronald Boellaard, Chantal Roth, Emma R Mulder, Henk M W Verheul, C Willemien Menke-van der Houven van Oordt
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0155178 (2016)
OBJECTIVE:The aim of this pilot study was to explore intrapatient mixed metabolic response and early 18F-FDG PET response evaluation using predefined quantification strategies in patients with advanced KRAS wild-type colorectal adenocarcinoma (mCRC)
Externí odkaz:
https://doaj.org/article/49091125a27f4fd896e56f6e516d9af6
Autor:
Hassan El Bouazzaoui, T.L.Th.A. Jansen, Sakir Akin, Erik J van Helden, Vincent van Driel, Remon Baak, Ronne A T A Mairuhu, Ingrid M. Garrelds, Koen Verdonk, Jan Kees van Rooden, Evert de Jonge, Iwan A. Meynaar, Kadir Caliskan, Johannes F A B Duynstee, Paula Schriek, Jeroen Ludikhuize, Ron H.N. van Schaik, Cees van Nieuwkoop, Rugina I. Neuman, A.H. Jan Danser, Loes E. Visser, Marjan Veuger, Lettie van den Berg
Publikováno v:
Journal of Hypertension, 40(3), 606-614. Lippincott Williams & Wilkins
Background The severity of COVID-19 after SARS-CoV-2 infection is unpredictable. Angiotensin-converting enzyme-2 (ACE2) is the receptor responsible for coronavirus binding, while subsequent cell entry relies on priming by the serine protease TMPRSS2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d366b02e15b6349af19963c5c2b1b3c7
https://pure.eur.nl/en/publications/3da63918-d30a-41a0-a1cc-51d970d63c3a
https://pure.eur.nl/en/publications/3da63918-d30a-41a0-a1cc-51d970d63c3a
Autor:
Erik J van Helden, Sjoerd G. Elias, Henk M.W. Verheul, Elisabeth G.E. de Vries, Suzanne C van Es, Astrid Aplonia Maria Van Der Veldt, Sarah R. Verhoeff, Erik H.J.G. Aarntzen, Sjoukje F. Oosting, Winette T. A. van der Graaf, Sandra Heskamp, Otto S. Hoekstra, Otto C. Boerman, Lindsay Angus, Wim J.G. Oyen, Carla M.L. van Herpen, Thomas C. Kwee, Adrienne H. Brouwers, Eline Boon
Publikováno v:
Verhoeff, S R, van Es, S C, Boon, E, van Helden, E, Angus, L, Elias, S G, Oosting, S F, Aarntzen, E H, Brouwers, A H, Kwee, T C, Heskamp, S, Hoekstra, O S, Verheul, H, van der Veldt, A A M, de Vries, E G E, Boerman, O C, van der Graaf, W T A, Oyen, W J G & van Herpen, C M L 2019, ' Lesion detection by [89Zr]Zr-DFO-girentuximab and [18F]FDG-PET/CT in patients with newly diagnosed metastatic renal cell carcinoma ', European Journal of Nuclear Medicine and Molecular Imaging, vol. 46, no. 9, pp. 1931-1939 . https://doi.org/10.1007/s00259-019-04358-9
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931-1939. Springer-Verlag
European Journal of Nuclear Medicine and Molecular Imaging, 46, 1931-1939
European Journal of Nuclear Medicine and Molecular Imaging
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931. Springer Verlag
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931-1939. Springer Verlag
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931-1939. SPRINGER
European Journal of Nuclear Medicine and Molecular Imaging, 46, 9, pp. 1931-1939
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931-1939. Springer-Verlag
European Journal of Nuclear Medicine and Molecular Imaging, 46, 1931-1939
European Journal of Nuclear Medicine and Molecular Imaging
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931. Springer Verlag
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931-1939. Springer Verlag
European Journal of Nuclear Medicine and Molecular Imaging, 46(9), 1931-1939. SPRINGER
European Journal of Nuclear Medicine and Molecular Imaging, 46, 9, pp. 1931-1939
Purpose The main objective of this preliminary analysis of the IMaging PAtients for Cancer drug selecTion (IMPACT)-renal cell cancer (RCC) study is to evaluate the lesion detection of baseline contrast-enhanced CT, [89Zr]Zr-DFO-girentuximab-PET/CT an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18fa35968023bca2a3e9f115930859d3
https://dspace.library.uu.nl/handle/1874/389954
https://dspace.library.uu.nl/handle/1874/389954
Autor:
Elisabeth G.E. de Vries, Derk Jan A. de Groot, Ronald Boellaard, Eline Boon, Carla M.L. van Herpen, Erik J van Helden, Otto S. Hoekstra, Catharina Wilhelmina Menke, Marc C. Huisman, Henk M.W. Verheul, Suzanne C van Es
Publikováno v:
Journal of Clinical Oncology, 35. American Society of Clinical Oncology
Van Helden, E J, Menke, C W, Boon, E, van Es, S, Huisman, M C, De Groot, D J, Boellaard, R, Van Herpen, C M L, De Vries, E, Hoekstra, O S & Verheul, H M W 2017, ' Change in metabolic tumor activity on F-18-FDG PET after a single dose of cetuximab to predict for treatment benefit, PFS, and OS in patients with advanced colorectal cancer. ', Journal of Clinical Oncology, vol. 35 . https://doi.org/10.1200/JCO.2017.35.15_suppl.11519
Van Helden, E J, Menke, C W, Boon, E, van Es, S, Huisman, M C, De Groot, D J, Boellaard, R, Van Herpen, C M L, De Vries, E, Hoekstra, O S & Verheul, H M W 2017, ' Change in metabolic tumor activity on F-18-FDG PET after a single dose of cetuximab to predict for treatment benefit, PFS, and OS in patients with advanced colorectal cancer. ', Journal of Clinical Oncology, vol. 35 . https://doi.org/10.1200/JCO.2017.35.15_suppl.11519
11519 Background: Despite RAS selection, one third of patients with metastatic RAS wild-type colorectal cancer (mCRC) do not benefit from anti-EGFR inhibitors. Therefore, an additional or more accurate predictive biomarker is needed to identify patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5931a76db24180addbba3c2c96a25c95
https://research.vumc.nl/en/publications/33513561-089f-4969-aa6c-308d5b92cd4d
https://research.vumc.nl/en/publications/33513561-089f-4969-aa6c-308d5b92cd4d
Autor:
Suzanne C van Es, Elisabeth G.E. de Vries, Danielle J. Vugts, Erik J van Helden, Otto S. Hoekstra, G.A.M.S. (Guus) van Dongen, Derk Jan A. de Groot, Henk M.W. Verheul, Marc C. Huisman, Catharina Wilhelmina Menke, Eline Boon, Carla M.L. van Herpen
Publikováno v:
Journal of Clinical Oncology. 35:e15117-e15117
e15117 Background: One third of patients with RAS wild-type metastatic colorectal cancer (mCRC) do not benefit from anti-EGFR inhibitors. Thus, predictive biomarkers to identify patients with primary resistant mCRC are urgently needed. Methods: Patie
Autor:
E. Mulder, Chantal Roth, Henk M.W. Verheul, Erik J van Helden, C. Willemien Menke-van der Houven van Oordt, Otto S. Hoekstra, Ronald Boellaard
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 5, p e0155178 (2016)
van Helden, E J, Hoekstra, O S, Boellaard, R, Roth, C, Mulder, E R, Verheul, H M W & Menke-van der Houven van Oordt, C 2016, ' Early F-18-FDG PET/CT Evaluation Shows Heterogeneous Metabolic Responses to Anti-EGFR Therapy in Patients with Metastatic Colorectal Cancer ', PLoS ONE, vol. 11, no. 5, e0155178 . https://doi.org/10.1371/journal.pone.0155178
PLoS ONE, 11(5):e0155178. Public Library of Science
PLoS ONE, Vol 11, Iss 5, p e0155178 (2016)
van Helden, E J, Hoekstra, O S, Boellaard, R, Roth, C, Mulder, E R, Verheul, H M W & Menke-van der Houven van Oordt, C 2016, ' Early F-18-FDG PET/CT Evaluation Shows Heterogeneous Metabolic Responses to Anti-EGFR Therapy in Patients with Metastatic Colorectal Cancer ', PLoS ONE, vol. 11, no. 5, e0155178 . https://doi.org/10.1371/journal.pone.0155178
PLoS ONE, 11(5):e0155178. Public Library of Science
OBJECTIVE:The aim of this pilot study was to explore intrapatient mixed metabolic response and early 18F-FDG PET response evaluation using predefined quantification strategies in patients with advanced KRAS wild-type colorectal adenocarcinoma (mCRC)
Autor:
Henk M.W. Verheul, Otto S. Hoekstra, Erik F. J. de Vries, Andor W. J. M. Glaudemans, Jim Janssen, Carl Moons, Winette van de Graaf, Lioe-Fee de Geus-Oei, Frederike Bensch, Liesbeth de Vries, Eline Boon, S.G. Elias, Erik J van Helden, Carolien P. Schröder, Adrienne H. Brouwers, Marc C. Huisman, Eric J. W. Visser, Willemien Menke-van der Hoeven van Oordt, Johan de Jong, Wim J.G. Oyen
Publikováno v:
Cancer Research. 75:OT3-2
Background: Therapy of newly identified MBC is largely based on estrogen receptor (ER) and human epidermal growth factor receptor 2 (HER2) status. Optimal receptor information should be up-to-date and preferably from the whole body, given receptor co