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C A Fijen

Showing results (21-30 of 30) with videos related to

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European Journal of Human Genetics : EJHG|July 26, 2000
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studiesR van den Bogaard, C A Fijen, M G Schipper, et al.
Journal of Clinical Microbiology|September 1, 1994
Characterization of strains of Neisseria meningitidis recovered from complement-sufficient and complement-deficient patients in the Western Cape Province, South AfricaA Orren, D A Caugant, C A Fijen, et al.
Clinical and Experimental Immunology|November 1, 1995
Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiencyC A Fijen, B H Derkx, E J Kuijper, et al.
Immunopharmacology|February 26, 1998
Human properdin deficiency has a heterogeneous genetic backgroundL Truedsson, J Westberg, G N Fredrikson, et al.
Clinical and Experimental Immunology|February 24, 1998
Meningococcal disease and polymorphism of FcgammaRIIa (CD32) in late complement component-deficient individualsA E Platonov, E J Kuijper, I V Vershinina, et al.
Immunology|December 1, 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 erythrocytesR G Bredius, C A Fijen, M De Haas, et al.
Clinical and Experimental Immunology|September 1, 1996
Heterozygous and homozygous factor H deficiency states in a Dutch familyC A Fijen, E J Kuijper, M Te Bulte, et al.
The Journal of Infectious Diseases|October 1, 1994
Fc gamma receptor IIa (CD32) polymorphism in fulminant meningococcal septic shock in childrenR G Bredius, B H Derkx, C A Fijen, et al.
Clinical and Experimental Immunology|May 3, 2000
The role of Fcgamma receptor polymorphisms and C3 in the immune defence against Neisseria meningitidis in complement-deficient individualsC A Fijen, R G Bredius, E J Kuijper, et al.
Molecular Immunology|March 4, 2000
Properdin deficiency: molecular basis and disease associationC A Fijen, R van den Bogaard, M Schipper, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
European Journal of Human Genetics : EJHG|July 26, 2000
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studiesR van den Bogaard, C A Fijen, M G Schipper, et al.
Journal of Clinical Microbiology|September 1, 1994
Characterization of strains of Neisseria meningitidis recovered from complement-sufficient and complement-deficient patients in the Western Cape Province, South AfricaA Orren, D A Caugant, C A Fijen, et al.
Clinical and Experimental Immunology|November 1, 1995
Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiencyC A Fijen, B H Derkx, E J Kuijper, et al.
Immunopharmacology|February 26, 1998
Human properdin deficiency has a heterogeneous genetic backgroundL Truedsson, J Westberg, G N Fredrikson, et al.
Clinical and Experimental Immunology|February 24, 1998
Meningococcal disease and polymorphism of FcgammaRIIa (CD32) in late complement component-deficient individualsA E Platonov, E J Kuijper, I V Vershinina, et al.
Immunology|December 1, 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 erythrocytesR G Bredius, C A Fijen, M De Haas, et al.
Clinical and Experimental Immunology|September 1, 1996
Heterozygous and homozygous factor H deficiency states in a Dutch familyC A Fijen, E J Kuijper, M Te Bulte, et al.
The Journal of Infectious Diseases|October 1, 1994
Fc gamma receptor IIa (CD32) polymorphism in fulminant meningococcal septic shock in childrenR G Bredius, B H Derkx, C A Fijen, et al.
Clinical and Experimental Immunology|May 3, 2000
The role of Fcgamma receptor polymorphisms and C3 in the immune defence against Neisseria meningitidis in complement-deficient individualsC A Fijen, R G Bredius, E J Kuijper, et al.
Molecular Immunology|March 4, 2000
Properdin deficiency: molecular basis and disease associationC A Fijen, R van den Bogaard, M Schipper, et al.
Pageof 3