Zobrazeno 1 - 10
of 21
pro vyhledávání: '"P G Hoogeveen"'
Autor:
Inge van Outersterp, Vincent H.J. van der Velden, Patricia G. Hoogeveen, Goda E. Vaitkevičienė, Edwin Sonneveld, Gijs van Haaften, Roland P. Kuiper, Udo zur Stadt, Gabriele Escherich, Judith M. Boer, Monique L. den Boer
Publikováno v:
HemaSphere, Vol 7, Iss 10, p e967 (2023)
Externí odkaz:
https://doaj.org/article/ef1fe8fac5a545b3a961b76a6c0583e7
Autor:
Monique L. den Boer, Harma Feitsma, Reno Bladergroen, Edwin Sonneveld, Roland P. Kuiper, Vincent H.J. van der Velden, Irina Sergeeva, Freerk van Dijk, Judith M. Boer, Frank N. van Leeuwen, P G Hoogeveen
Publikováno v:
British Journal of Haematology, 194(5), 888-892. Wiley-Blackwell Publishing Ltd
Minimal residual disease (MRD) diagnostics are implemented in most clinical protocols for patients with acute lymphoblastic leukaemia (ALL) and are mostly performed using rearranged immunoglobulin (IG) and/or T-cell receptor (TR) gene rearrangements
Autor:
P G Hoogeveen, Vincent H.J. van der Velden, H. Berna Beverloo, Edwin Sonneveld, Rianne Noordijk, Anneke Koning-Goedheer, Maaike de Bie
Publikováno v:
Leukemia & Lymphoma, 59(6), 1508-1510. Informa Healthcare
Monitoring of minimal residual disease (MRD) has become routine clinical practice in frontline treatment of virtually all childhood acute lymphoblastic leukemia (ALL) and many adult ALL patients [1...
Autor:
Vincent H.J. van der Velden, Jacques J.M. van Dongen, Nicole S. D. Larmonie, H. Berna Beverloo, P G Hoogeveen, Willem A. Dik, Anton W. Langerak, Jules P.P. Meijerink
Publikováno v:
British Journal of Haematology. 157:142-146
Autor:
Tomas Kalina, V H J van der Velden, F J T Staal, P G Hoogeveen, Alberto Orfao, Paulo Sérgio Lucio, Monika Brüggemann, Martin Kovac, Nancy Boeckx, Edwin Sonneveld, Juan Flores-Montero, A. Koning-Goedheer, Lukasz Sedek, W.M. Comans-Bitter, J. J. M. Van Dongen, Paul Evans, E Dekking, S Böttcher, Tomasz Szczepański
Publikováno v:
Best Practice & Research Clinical Haematology, 23(3), 333-345. Elsevier
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
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Nowadays, the presence of specific genetic aberrations is progressively used for classification and treatment stratification, because acute leukemias with the same oncogenetic aberration generally form a clinically and diagnostically homogenous disea
Autor:
P G Hoogeveen, Mark Brussee, C. Ellen van der Schoot, Valerie de Haas, Christa Homburg, Jacques J.M. van Dongen, Vincent H.J. van der Velden, Rianne Noordijk
Publikováno v:
British journal of haematology, 164(3), 451-453. Wiley-Blackwell
British Journal of Haematology, 164(3), 451-453. Wiley-Blackwell Publishing Ltd
British Journal of Haematology, 164(3), 451-453. Wiley-Blackwell Publishing Ltd
Autor:
P G Hoogeveen, Elisabeth R. van Wering, Vincent H.J. van der Velden, Jacques J.M. van Dongen, Maaike de Bie, Tomasz Szczepański, Daniëlle C. H. Jacobs
Publikováno v:
Blood. 103:3798-3804
The frequently occurring T-cell receptor delta (TCRD) deletions in precursor-B-acute lymphoblastic leukemia (precursor-B-ALL) are assumed to be mainly caused by Vdelta2-Jalpha rearrangements. We designed a multiplex polymerase chain reaction tified c
Autor:
Nancy Boeckx, J. G. te Marvelde, V H J van der Velden, J J van Dongen, I Jedema, P G Hoogeveen, Marc Boogaerts
Publikováno v:
Leukemia, 18, 983-988. Nature Publishing Group
Gemtuzumab ozogamicin (Mylotarg) induces remission in approximately 30% of relapsed AML patients. We previously demonstrated that gemtuzumab infusion results in near-complete CD33 saturation in peripheral blood, and that saturating gemtuzumab levels
Autor:
V H J van der Velden, W C J Hop, P G Hoogeveen, P G Hart, J M Wijkhuijs, E. R. Van Wering, Tomasz Szczepański, J. J. M. Van Dongen
Publikováno v:
Leukemia, 17, 1834-1844. Nature Publishing Group
Detailed Southern blot and PCR analysis of Ig heavy (IGH), Ig kappa (IGK), T-cell receptor delta (TCRD), and TCR gamma (TCRG) genes were performed in 289 children with precursor-B-ALL in order to determine age-related Ig/TCR patterns and their implic
Autor:
Menno C. van Zelm, Kirsten van Lom, Magdalena Schindler-van der Struijk, Pieternella J. Lugtenburg, P G Hoogeveen, King H. Lam, Vincent H.J. van der Velden, Dick de Ridder, Dennis Karsch, Alberto Orfao, Mathijs A. Sanders, Jacques J.M. van Dongen, H. Berna Beverloo, Sebastian Böttcher, Mies C. Kappers-Klunne, Anton W. Langerak
Publikováno v:
Blood. 124(3)
B-cell prolymphocytic leukemia (B-PLL) is a rare mature B-cell malignancy that may be hard to distinguish from mantle cell lymphoma (MCL) and chronic lymphocytic leukemia (CLL). B-PLL cases with a t(11;14) were redefined as MCL in the World Health Or