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

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

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

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

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

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

ανά 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.
Έκδοση 2010

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

ανά 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
Τόπος έκδοσης Bone Marrow Transplant (2005)

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

ανά 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
Έκδοση 2000

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

ανά 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
Έκδοση 2014

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

ανά 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.
Τόπος έκδοσης Orphanet J Rare Dis (2019)

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

ανά 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
Τόπος έκδοσης Pediatr Rheumatol Online J (2015)