Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Joyce H. Radersma-van Loon"'
Autor:
Peter E. Westerweel, Joyce H. Radersma-van Loon, Roos J. Leguit, Manon M. H. Huibers, Laura S. Hiemcke-Jiwa, Monique C. Minnema, Johannes J.M. Rood, Jeanette K. Doorduijn
Publikováno v:
Leukemia & Lymphoma, 59(5), 1256-1259. Informa Healthcare
Lymphoplasmacytic lymphoma (LPL) is a low-grade B-cell non-Hodgkin lymphoma that typically involves the bone marrow, lymph nodes and spleen and usually has an indolent course. Transformation to a d...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::659ba2c1d6690601240fa18d0d0e1728
https://doi.org/10.1080/10428194.2017.1369074
https://doi.org/10.1080/10428194.2017.1369074
Autor:
Monique C. Minnema, Manon M. H. Huibers, Laura S. Hiemcke-Jiwa, Joyce H. Radersma-van Loon, Mirthe de Boer, N. Mehdi Jiwa, Roos J. Leguit, Roel A. de Weger
Publikováno v:
Hematological oncology. 36(2)
The gold standard for diagnosis of central nervous system lymphomas still regards a stereotactic brain biopsy, with the risk of major complications for the patient. As tumor cells can be detected in cerebrospinal fluid (CSF), CSF analysis can be used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99ef20e416a795e6dd9b1ce5b09acbbc
https://pubmed.ncbi.nlm.nih.gov/29210102
https://pubmed.ncbi.nlm.nih.gov/29210102
Autor:
Marco J. Koudijs, John W. J. Hinrichs, Joyce H. Radersma-van Loon, Sophia B Rappel, Stefan M. Willems, W. T. Marja van Blokland, Michiel J. Moons, Nicolle Besselink, Roel A. de Weger, Carmen M. A. de Voijs, Remco D. Radersma
Publikováno v:
American journal of clinical pathology, 143(4), 573. American Society of Clinical Pathologists
Objectives: To compare next-generation sequencing (NGS) platforms with mutation-specific analysis platforms in a clinical setting, in terms of sensitivity, mutation specificity, costs, capacity, and ease of use. Methods: We analyzed 25 formalin-fixed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5d8afc5ac4bf4d1a3f483d66de4b0c
https://dspace.library.uu.nl/handle/1874/331338
https://dspace.library.uu.nl/handle/1874/331338
Autor:
Nicolle Besselink, Carmen M. A. de Voijs, Marco J. Koudijs, John W. J. Hinrichs, Roel A. de Weger, Isaac J. Nijman, Stefan M. Willems, Ton Peeters, Edwin Cuppen, Marlous Hoogstraat, Emile E. Voest, Joyce H. Radersma-van Loon
Publikováno v:
Journal of Molecular Diagnostics, 17(1), 10. Association of Molecular Pathology
Journal of Molecular Diagnostics, 17(1), 10-8. Association of Molecular Pathology
Journal of Molecular Diagnostics, 17(1), 10-8. Association of Molecular Pathology
In routine cancer molecular pathology, various independent experiments are required to determine mutation and amplification status of clinically relevant genes. Most of these tests are designed to identify a limited number of genetic aberrations, mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ade28a7073136bb94188afee51045f58
https://dspace.library.uu.nl/handle/1874/331334
https://dspace.library.uu.nl/handle/1874/331334