Zobrazeno 1 - 10
of 30
pro vyhledávání: '"P. J. Van Dijken"'
Autor:
Jesse D de Groot, Bart R J van Dijken, Hiska L van der Weide, Roelien H Enting, Anouk van der Hoorn
Publikováno v:
PLoS ONE, Vol 18, Iss 5, p e0275077 (2023)
BackgroundRadiotherapy (RT) and chemotherapy are components of standard multi-modality treatment of high grade gliomas (HGG) aimed at achieving local tumor control. Treatment is neurotoxic and RT plays an important role in this, inducing damage even
Externí odkaz:
https://doaj.org/article/44bcde16c76b47849a4344b62bf293f8
Autor:
Bart R. J. van Dijken, Hanne-Rinck Jeltema, Justyna Kłos, Peter Jan van Laar, Roelien H. Enting, Ronald G. H. J. Maatman, Klaas Bijsterveld, Wilfred F. A. Den Dunnen, Rudi A. Dierckx, Paul E. Sijens, Anouk van der Hoorn
Publikováno v:
Diagnostics, Vol 13, Iss 17, p 2791 (2023)
Isocitrate dehydrogenase (IDH) mutation status is an important biomarker in the glioma-defining subtype and corresponding prognosis. This study proposes a straightforward method for 2-hydroxyglutarate (2-HG) quantification by MR spectroscopy for IDH
Externí odkaz:
https://doaj.org/article/88d6706036dd49d38b2cb0651fcfd264
Autor:
Bart R J van Dijken, Alfred O Ankrah, Gilles N Stormezand, Rudi A J O Dierckx, Peter Jan van Laar, Anouk van der Hoorn
Publikováno v:
PLoS ONE, Vol 17, Iss 2, p e0264387 (2022)
Purpose11C-Methionine (11C-MET) PET prognostication of isocitrate dehydrogenase (IDH) wild type glioblastomas is inadequate as conventional parameters such as standardized uptake value (SUV) do not adequately reflect tumor heterogeneity. We retrospec
Externí odkaz:
https://doaj.org/article/a6e5aedfd173486a845e1d9ed25347cd
Publikováno v:
Saudi medical journal. 20(1)
Full text is available as a scanned copy of the original print version.
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)
Autor:
Bernd H. Belohradsky, M. van Deuren, Ismail Reisli, M M Hagleitner, S.M. van der Maarel, Andrew R. Gennery, E. J. A. Gerritsen, P J Howard, Corry M.R. Weemaes, R de Groot, Jean-Pierre Fryns, Catharina Schuetz, Dieter Furthner, Maj Hultén, Anders Fasth, EG Davies, J.C. de Greef, P J van Dijken, Andrew J. Cant, Giorgio Gimelli, G Cazzola, Teresa Mattina, A.C. Lankester, Paola Maraschio, Mary Slatter
Publikováno v:
Journal of Medical Genetics, 45, 2, pp. 93-9
Journal of Medical Genetics, 45, 93-9
Journal of Medical Genetics, 45, 93-9
Contains fulltext : 69091.pdf (Publisher’s version ) (Closed access) BACKGROUND: Immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome) is a rare autosomal recessive disease characterised by facial dysmorphism, immunoglobul
Publikováno v:
Tijdschrift voor kindergeneeskunde. 73:42-45
Door de toegenomen mogelijkheden om infecties door Bartonella henselae te diagnosticeren, blijkt kattenkrabziekte een breed spectrum aan verschijningsvormen te hebben. We beschrijven drie patienten. Een 5-jarig meisje met een typische lymfadenitis me
Publikováno v:
Blood. 78:2773-2779
We have examined the effect of graft-versus-host disease (GVHD) on the reconstitution of donor hematopoiesis in a murine bone marrow transplant (BMT) model of GVHD to minor histocompatibility antigens. GVHD had no effect on peripheral blood counts, w
Publikováno v:
Transplantation. 49:882-885
The LFA-1 molecule is a member of the leukocyte adhesion complex (CD11/CD18) that is critical to adhesion and effector function of T cells and NK cells. Both T cells and NK cells play important roles in bone marrow graft rejection, and anti-LFA-1 MAb
Autor:
P. J. van Dijken, Harold Verbakel, M. Herremans, A.M.C. Bergmans, Marcel F. Peeters, Marijn J. Vermeulen, J. J. Roord
Publikováno v:
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases. 13(6)
Cat-scratch disease (CSD), caused by Bartonella henselae infection, can mimic malignancy and can manifest atypically. Reliable serological testing is therefore of great clinical importance. The diagnostic performance of immunofluorescence assay (IFA)
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 149(42)
4 children, a boy aged 10 years and 3 girls aged 3, 3, and 16 years, suffering from chronic or refractory autoimmune haemolytic anaemia (AIHA), who were dependent on high doses of steroids and were refractory to immunosuppressants, were treated with