Complement activation by polyclonal immunoglobulin G1 and G2 antibodies against Staphylococcus aureus, Haemophilus influenzae type b, and tetanus toxoid.

par Bredius, R G, Driedijk, P C, Schouten, M F, Weening, R S, Out, T A
Publié 1992

Quantitative flow cytometric analysis of opsonophagocytosis and killing of nonencapsulated Haemophilus influenzae by human polymorphonuclear leukocytes.

par Vogel, L, van Alphen, L, Geluk, F, Troelstra, A, Martin, E, Bredius, R, Eijk, P, Jansen, H, Dankert, J
Publié 1994

Role of neutrophil Fc gamma RIIa (CD32) and Fc gamma RIIIb (CD16) polymorphic forms in phagocytosis of human IgG1- and IgG3-opsonized bacteria and erythrocytes.

par Bredius, R G, Fijen, C A, De Haas, M, Kuijper, E J, Weening, R S, Van de Winkel, J G, Out, T A
Publié 1994

Campylobacter jejuni bacteremia and Helicobacter pylori in a patient with X-linked agammaglobulinemia

par van den Bruele, T., Mourad-Baars, P. E. C., Claas, E. C. J., van der Plas, R. N., Kuijper, E. J., Bredius, R. G. M.
Publié 2010

Allogeneic bone marrow transplantation for juvenile myelomonocytic leukemia: a single center experience of 23 patients

par Korthof, E T, Snijder, P P, de Graaff, A A, Lankester, A C, Bredius, R G M, Ball, L M, Lie, J L W T, Vossen, J M, Egeler, R M
Publié dans Bone Marrow Transplant (2005)

The role of Fcγ receptor polymorphisms and C3 in the immune defence against Neisseria meningitidis in complement-deficient individuals

par Fijen, C A P, Bredius, R G M, Kuijper, E J, Out, T A, De Haas, M, De Wit, A P M, Daha, M R, Van De Winkel, J G J
Publié 2000

A new functional assay for the diagnosis of X-linked inhibitor of apoptosis (XIAP) deficiency

par Ammann, S, Elling, R, Gyrd-Hansen, M, Dückers, G, Bredius, R, Burns, S O, Edgar, J D M, Worth, A, Brandau, H, Warnatz, K, zur Stadt, U, Hasselblatt, P, Schwarz, K, Ehl, S, Speckmann, C
Publié 2014

Effects of immunomodulation in classic infantile Pompe patients with high antibody titers

par Poelman, E., Hoogeveen-Westerveld, M., van den Hout, J. M. P., Bredius, R. G. M., Lankester, A. C., Driessen, G. J. A., Kamphuis, S. S. M., Pijnappel, W. W. M., van der Ploeg, A. T.
Publié dans Orphanet J Rare Dis (2019)

Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations

par Van Montfrans, J, Hartman, E, Braun, K, Hennekam, F, Hak, A, Nederkoorn, P, Westendorp, W, Bredius, R, Kollen, W, Scholvinck, E, Legger, G, Meyts, I, Liston, A, Lichtenbelt, K, Giltay, J, Van Haaften, G, De Vries Simons, G, Leavis, H, Nierkens, S, Sanders, C, Van Gijn, M
Publié dans Pediatr Rheumatol Online J (2015)