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

Por Bredius, R G, Driedijk, P C, Schouten, M F, Weening, R S, Out, T A
Publicado em 1992

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

Por Vogel, L, van Alphen, L, Geluk, F, Troelstra, A, Martin, E, Bredius, R, Eijk, P, Jansen, H, Dankert, J
Publicado em 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.

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

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

Por 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.
Publicado em 2010

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

Por 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
Publicado no Bone Marrow Transplant (2005)

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

Por 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
Publicado em 2000

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

Por 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
Publicado em 2014

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

Por 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.
Publicado no Orphanet J Rare Dis (2019)

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

Por 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
Publicado no Pediatr Rheumatol Online J (2015)