Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Bas, Vaarwerk"'
Autor:
Isabelle S. A. de Vries, Roelof van Ewijk, Laura M. E. Adriaansen, Anneloes E. Bohte, Arthur J. A. T. Braat, Raquel Dávila Fajardo, Laura S. Hiemcke-Jiwa, Marinka L. F. Hol, Simone A. J. ter Horst, Bart de Keizer, Rutger R. G. Knops, Michael T. Meister, Reineke A. Schoot, Ludi E. Smeele, Sheila Terwisscha van Scheltinga, Bas Vaarwerk, Johannes H. M. Merks, Rick R. van Rijn
Publikováno v:
Pediatric Radiology. 53:788-812
Rhabdomyosarcoma, although rare, is the most frequent soft tissue sarcoma in children and adolescents. It can present as a mass at nearly any site in the body, with most common presentations in the head and neck, genitourinary tract and extremities.
Autor:
Isabelle S. A. de Vries, Roelof van Ewijk, Laura M. E. Adriaansen, Anneloes E. Bohte, Arthur J. A. T. Braat, Raquel Dávila Fajardo, Laura S. Hiemcke‑Jiwa, Marinka L. F. Hol, Simone A. J. ter Horst, Bart de Keizer, Rutger R. G. Knops, Michael T. Meister, Reineke A. Schoot, Ludi E. Smeele, Sheila Terwisscha van Scheltinga, Bas Vaarwerk, Johannes H. M. Merks, Rick R. van Rijn
Publikováno v:
Pediatric Radiology. 53:1043-1043
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 165
Children treated for rhabdomyosarcoma are subject to protocolized follow-up imaging to detect a potential relapse earlier and to improve the chances of survival in case of a relapse. In this study we report on our findings concerning the clinical val
Autor:
Bas Vaarwerk, Willemijn B Breunis, Lianne M Haveman, Bart de Keizer, Nina Jehanno, Lise Borgwardt, Rick R van Rijn, Henk van den Berg, Jérémie F Cohen, Elvira C van Dalen, Johannes HM Merks
Publikováno v:
The Cochrane Library
Cochrane Database Syst Rev
Cochrane Database Syst Rev
BACKGROUND: Rhabdomyosarcoma (RMS) is the most common paediatric soft‐tissue sarcoma and can emerge throughout the whole body. For patients with newly diagnosed RMS, prognosis for survival depends on multiple factors such as histology, tumour site,
Publikováno v:
Cancers. 15:66
The foundations of evidence-based practice are the triad of patient values and preferences, healthcare professional experience, and best available evidence, used together to inform clinical decision-making. Within the field of rhabdomyosarcoma, colla
Autor:
M. C. Naafs-Wilstra, Bas Vaarwerk, Martha A. Grootenhuis, Johannes H. M. Merks, P. F. Limperg
Publikováno v:
Supportive Care in Cancer
Supportive Care in Cancer, 27(10), 3841-3848. Springer Verlag
Vaarwerk, B, Limperg, P F, Naafs-Wilstra, M C, Merks, J H M & Grootenhuis, M A 2019, ' Getting control during follow-up visits: the views and experiences of parents on tumor surveillance after their children have completed therapy for rhabdomyosarcoma or Ewing sarcoma ', Supportive Care in Cancer, vol. 27, no. 10, pp. 3841-3848 . https://doi.org/10.1007/s00520-019-04678-4
Supportive care in cancer, 27(10), 3841-3848. Springer Verlag
Supportive Care in Cancer, 27(10), 3841-3848. Springer Verlag
Vaarwerk, B, Limperg, P F, Naafs-Wilstra, M C, Merks, J H M & Grootenhuis, M A 2019, ' Getting control during follow-up visits: the views and experiences of parents on tumor surveillance after their children have completed therapy for rhabdomyosarcoma or Ewing sarcoma ', Supportive Care in Cancer, vol. 27, no. 10, pp. 3841-3848 . https://doi.org/10.1007/s00520-019-04678-4
Supportive care in cancer, 27(10), 3841-3848. Springer Verlag
Purpose: Patients treated for rhabdomyosarcoma (RMS) or Ewing sarcoma (ES) are subject to extensive follow-up after completion of therapy. The aim of this follow-up is to monitor treatment side effects and to detect relapse in an early phase to impro
Autor:
Gian Luca De Salvo, Gianni Bisogno, Meriel Jenney, Carlo Morosi, Daniel Orbach, Bas Vaarwerk, Ilaria Zanetti, Hervé Brisse, Andrea Ferrari, Julia C. Chisholm, Johannes H. M. Merks, Kieran McHugh, Nadège Corradini, Rick R. van Rijn
Publikováno v:
Journal of clinical oncology, 37(9), 723-730. American Society of Clinical Oncology
Purpose To evaluate the clinical significance of indeterminate pulmonary nodules at diagnosis (defined as ≤ 4 pulmonary nodules < 5 mm or 1 nodule measuring ≥ 5 and < 10 mm) in patients with pediatric rhabdomyosarcoma (RMS). Patients and Methods
Autor:
Bas Vaarwerk, Simone A. J. ter Horst, Roelof van Ewijk, Rick R. van Rijn, Reineke A. Schoot, Johannes H. M. Merks, Willemijn B. Breunis, Johanna H. van der Lee
Publikováno v:
Cancers
Cancers, Vol 13, Iss 510, p 510 (2021)
Cancers, Vol 13, Iss 510, p 510 (2021)
Simple Summary Rhabdomyosarcoma is the most common soft tissue sarcoma in childhood. At diagnosis, tumor and patient characteristics determine the prognosis and subsequent treatment stratification. There are currently no early biomarkers that identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab8f75d7ebfd748913d34d6fa82c70ac
https://doi.org/10.5167/uzh-212920
https://doi.org/10.5167/uzh-212920
Autor:
Daniel Orbach, Soledad Gallego, Meriel Jenney, Nathalie Cozic, Johanna H. van der Lee, Bas Vaarwerk, Christine Devalck, Johannes H. M. Merks, Willemijn B. Breunis, Anna Kelsey, Michael C. Stevens, Kieran McHugh, Odile Oberlin, Rick R. van Rijn, Mark N. Gaze, Julia C. Chisholm, Christophe Bergeron, Heidi Glosli, Veronique Minard-Colin
Publikováno v:
Cancer. 124:1016-1024
BACKGROUND: Early response to induction chemotherapy is used in current European guidelines to evaluate the efficacy of chemotherapy and subsequently to adapt treatment in pediatric patients with rhabdomyosarcoma (RMS). However, existing literature o
Autor:
Huib N. Caron, Simon D. Strackee, Olga Slater, Johannes H. M. Merks, Eva Gajdosova, Bradley R. Pieters, Ludi E. Smeele, Raquel Dávila Fajardo, Michiel W. M. van den Brekel, Marinka L.F. Hol, Reineke A. Schoot, Benjamin Hartley, Henry Mandeville, Stefanie van Jaarsveld, Peerooz Saeed, Bas Vaarwerk, Martha A. Grootenhuis, Heleen Maurice-Stam, Mark N. Gaze, Julia C. Chisholm, Leontien C. M. Kremer, Cécile M. Ronckers, Alfons J. M. Balm, David Dunaway
Publikováno v:
Vaarwerk, B, Schoot, R A, Maurice-Stam, H, Slater, O, Hartley, B, Saeed, P, Gajdosova, E, van den Brekel, M W, Balm, A J M, Hol, M L F, van Jaarsveld, S, Kremer, L C M, Ronckers, C M, Mandeville, H C, Pieters, B R, Gaze, M N, Davila Fajardo, R, Strackee, S D, Dunaway, D, Smeele, L E, Chisholm, J C, Caron, H N, Grootenhuis, M A & Merks, J H M 2019, ' Psychosocial well-being of long-term survivors of pediatric head-neck rhabdomyosarcoma ', Pediatric Blood & Cancer, vol. 66, no. 2, e27498 . https://doi.org/10.1002/pbc.27498
Pediatric Blood & Cancer, 66(2), e27498. Wiley-Liss Inc.
Pediatric Blood & Cancer, 66(2):e27498. Wiley-Liss Inc.
Pediatric Blood and Cancer, 66(2):e27498. Wiley-Liss Inc.
Pediatric blood & cancer, 66(2):e27498. Wiley-Liss Inc.
Pediatric Blood & Cancer, 66(2), e27498. Wiley-Liss Inc.
Pediatric Blood & Cancer, 66(2):e27498. Wiley-Liss Inc.
Pediatric Blood and Cancer, 66(2):e27498. Wiley-Liss Inc.
Pediatric blood & cancer, 66(2):e27498. Wiley-Liss Inc.
Background: Head and neck rhabdomyosarcoma (HNRMS) survivors are at risk to develop adverse events (AEs). The impact of these AEs on psychosocial well‐being is unclear. We aimed to assess psychosocial well‐being of HNRMS survivors and examine whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9a669f89b68f07e19846213ddcb5f93
https://hdl.handle.net/11245.1/8e5202ec-558d-418d-80c1-4e7757d28b6c1871.1/37575f4b-a3cc-4789-b413-c032f4a64b82
https://hdl.handle.net/11245.1/8e5202ec-558d-418d-80c1-4e7757d28b6c1871.1/37575f4b-a3cc-4789-b413-c032f4a64b82