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

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

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

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

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

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

nork 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.
Argitaratua 2010

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

nork 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
Argitaratua izan da Bone Marrow Transplant (2005)

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

nork 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
Argitaratua 2000

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

nork 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
Argitaratua 2014

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

nork 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.
Argitaratua izan da Orphanet J Rare Dis (2019)

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

nork 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
Argitaratua izan da Pediatr Rheumatol Online J (2015)