Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Frederik van-Delft"'
Autor:
Uri Ilan, Judith M. Boer, Birgit Burkhardt, Frederik van Delft, Shai Izraeli, Jan-Henning Klusmann, Barbara De Moerloose, Pablo Velasco, Julie Irving, José Luis Fuster, Dániel Erdélyi, Andreas E Kulozik, Dirk Reinhardt, Michel Zwaan, Monique L. den Boer
Publikováno v:
HemaSphere, Vol 7, p e86945e6 (2023)
Externí odkaz:
https://doaj.org/article/f1708f804c6f49fcb9464343c4404e9d
Autor:
Fabian J. S. van der Velden, Frederik van Delft, Stephen Owens, Judit Llevadias, Michael McKean, Lindsey Pulford, Yusri Taha, Grace Williamson, Quentin Campbell-Hewson, Sophie Hambleton, Rebecca Payne, Christopher Duncan, Catriona Johnston, Jarmila Spegarova, Marieke Emonts
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Pulmonary severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children is generally described as mild, and SARS-CoV-2 infection in immunocompromised children are observed as generally mild as well. A small proportion of pediatri
Externí odkaz:
https://doaj.org/article/b9245f9eb95242f8b76032f328152c8a
Autor:
Frederik van-Delft, Simon Bailey, Kate Pearce, Richard Martin, Roderick Skinner, Geoff Shenton, Peter Carey, quentin campbell-hewson, Juliet Hale, leigh mcdonald, katrina robinson, gavin cuthbert
Publikováno v:
Pediatric Blood & Cancer.
This brief report describes the importance of close discussion between clinicians and scientists and progress in leukaemia genetic work-up to deliver optimal treatment to a girl with 2 episodes of childhood Acute Lymphoblastic Leukaemia. At initial p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9196a95e28a18dfb849e84ae2a79bdbc
https://doi.org/10.1002/pbc.30451
https://doi.org/10.1002/pbc.30451
Autor:
Rebecca R. Selzer, Frederik van Delft, Christine J. Harrison, Hazel M. Robinson, Jonathan C. Strefford
Publikováno v:
Blood. 106:2843-2843
A highly complex, rearranged chromosome 21, arising from duplication of 21q and associated with amplification of RUNX1 [dup(21q)], is linked to a poor prognosis in acute lymphoblastic leukemia (ALL). Using BAC array-based CGH (Spectral Genomics 1Mb,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a014c500edc5297d7bcc9ba1fc5ffce6
https://doi.org/10.1182/blood.v106.11.2843.2843
https://doi.org/10.1182/blood.v106.11.2843.2843