Zobrazeno 1 - 10 of 67 pro vyhledávání: '"R. S. Weening"'
1
Immune Complex Glomerulonephritis in Chronic Granulomatous Disease
Autor: D. J. Rhenen, M. I. Koolen, Th. M. Feltkamp‐Vroom, R. S. Weening
Publikováno v: Acta Medica Scandinavica. 206:233-237
An 18-year-old girl is described who developed advanced renal sclerotic lesions, probably preceded by local focal glomerulonephritis, which coexisted with a Staphylococcus aureus abscess. It is hypothesized that immune complex glomerulonephritis deve
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5a6d91104dff38e20e8ca05b1ea3a334
https://doi.org/10.1111/j.0954-6820.1979.tb13502.x
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2
Afwijkingen in fagocyten
Autor: T. W. Kuijpers, R. S. Weening
Publikováno v: Tijdschrift voor kindergeneeskunde. 70:29-35
Er wordt een korte beschrijving gegeven van neutropenieen en van afwijkingen in de granulocytenfunctie. Kwantitatieve stoornissen komen veel frequenter voor dan kwalitatieve. Dysfuncties kunnen zowel genetisch bepaald als verworven zijn. Ziektebeelde
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fbfb69483edfec748ada9eee4c3f55fb
https://doi.org/10.1007/bf03061367
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3
A single dose of granulocyte-macrophage colony-stimulating factor induces systemic interleukin-8 release and neutrophil activation in healthy volunteers
Autor: M. V. Huisman, D Roos, R. H. J. Van Oers, A. E. G. K. Von Dem Borne, R. S. Weening, L. J. Van Pelt
Publikováno v: Blood, 87(12), 5305-5313. American Society of Hematology
Granulocyte-macrophage colony-stimulating factor (GM-CSF) and granulocyte colony-stimulating factor (G-CSF) are frequently used in the clinical management of neutropenia. These cytokines not only enhance the proliferation of myeloid precursor cells b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8fae0e5694863ef0bcb10b173669e0
https://doi.org/10.1182/blood.v87.12.5305.bloodjournal87125305
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5
Fca Receptor Iia (Cd32) Polymorphism In Fulminant Meningococcal Septic
Autor: R. S. Weening, J. G. J. Van De Winkel, Theo A. Out, C. A. P. Fijen, B. H. F. Derkx, R. G. M. Bredius, M. de Haas, T. P. M. De Wit
Publikováno v: Journal of Infectious Diseases. 170:848-853
Antibodies are essential in host defense against Neisseria meningitidis. Therefore, interactions among IgG and Fc receptors (Fc gamma R) on phagocytes may be crucial. Genetic polymorphic forms of Fc gamma RIIa (CD32) express different functional acti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::204bea469dcf89e6f31bbdf36d5e6365
https://doi.org/10.1093/infdis/170.4.848
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6
Phagocytosis of Staphylococcus aureus and Haemophilus influenzae type B opsonized with polyclonal human IgG1 and IgG2 antibodies. Functional hFc gamma RIIa polymorphism to IgG2
Autor: R G Bredius, C E de Vries, A Troelstra, L van Alphen, R S Weening, J G van de Winkel, T A Out
Publikováno v: The Journal of Immunology. 151:1463-1472
To assess the function of IgG subclass antibodies we studied the opsonization of Staphylococcus aureus (STAW) and Haemophilus influenzae type b (Hib) by natural IgG1 and IgG2 antibodies from five healthy individuals. Phagocytosis by polymorphonuclear
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::57d0db54e2eb662816b0a7a17a16a2fb
https://doi.org/10.4049/jimmunol.151.3.1463
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7
Complement activation by polyclonal immunoglobulin G1 and G2 antibodies against Staphylococcus aureus, Haemophilus influenzae type b, and tetanus toxoid
Autor: Theo A. Out, M. F. J. Schouten, P. C. Driedijk, R. S. Weening, Robbert G. M. Bredius
Publikováno v: Scopus-Elsevier
To obtain information on effector functions of human immunoglobulin G2 (IgG2), we have measured the complement-activating properties of polyclonal IgG subclass antibodies against bacterial antigens. IgG1 and IgG2 were purified from serum samples from
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c817f850b2981d362a248be009b780e7
https://doi.org/10.1128/iai.60.11.4838-4847.1992
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8
Splice site mutations are a common cause of X-linked chronic granulomatous disease
Autor: M, de Boer, B G, Bolscher, M C, Dinauer, S H, Orkin, C I, Smith, A, Ahlin, R S, Weening, D, Roos
Publikováno v: Blood. 80:1553-1558
Chronic granulomatous disease (CGD) is characterized by the absence of a respiratory burst in activated phagocytes. Defects in at least four different genes lead to CGD. Patients with the X-linked form of CGD have mutations in the gene for the beta-s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9631a221ae3a6fbe7f477a16c3778929
https://doi.org/10.1182/blood.v80.6.1553.bloodjournal8061553
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9
A missense mutation in the heavy subunit of gamma-glutamylcysteine synthetase gene causes hemolytic anemia
Autor: E, Ristoff, C, Augustson, J, Geissler, T, de Rijk, K, Carlsson, J L, Luo, K, Andersson, R S, Weening, R, van Zwieten, A, Larsson, D, Roos
Publikováno v: Blood. 95(7)
gamma-Glutamylcysteine synthetase (GCS) catalyzes the initial and rate-limiting step in the biosynthesis of glutathione. gamma-GCS consists of a heavy and a light subunit encoded by separate genes. Hereditary deficiency of GCS has been reported in 6
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::07c856dc3fa49ee2837d87ac9b160f68
https://pubmed.ncbi.nlm.nih.gov/10733484
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