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Journal of Human Genetics
|
March 31, 2009
A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation
Esther van de Vosse, Annelies van Wengen, Jos A van Geelen, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 27, 2011
Phenotypic variation in IgG receptors by nonclassical FCGR2C alleles
Joris van der Heijden, Willemijn B Breunis, Judy Geissler, et al.
Immunology Letters
|
April 27, 2017
Mutation characterization and heterodimer analysis of patients with leukocyte adhesion deficiency: Including one novel mutation
Shahram Teimourian, Martin De Boer, Dirk Roos, et al.
Experimental Hematology
|
March 8, 2002
Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations
Dirk Roos, Christof Meischl, Martin de Boer, et al.
Molecular Immunology
|
December 9, 2008
High-throughput analysis of the C4 polymorphism by a combination of MLPA and isotype-specific ELISA's
Diana Wouters, Pauline van Schouwenburg, Anneke van der Horst, et al.
Human Mutation
|
January 31, 2014
Primary immunodeficiency caused by an exonized retroposed gene copy inserted in the CYBB gene
Martin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG
|
July 10, 2002
Decreased redox state in red blood cells from patients with sarcoidosis
Snjezana Rothkrantz-Kos, Marjolein Drent, Herma Vuil, et al.
Clinical and Vaccine Immunology : CVI
|
November 6, 2007
Mannose-binding lectin deficiency facilitates abdominal Candida infections in patients with secondary peritonitis
J W Olivier van Till, Piet W Modderman, Martin de Boer, et al.
Journal of Clinical Immunology
|
February 8, 2018
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A)
Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Clinical Immunology (Orlando, Fla.)
|
August 19, 2008
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patients
Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 74) with videos related to
Sort By:
Page
of 8
Journal of Human Genetics
|
March 31, 2009
A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation
Esther van de Vosse, Annelies van Wengen, Jos A van Geelen, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 27, 2011
Phenotypic variation in IgG receptors by nonclassical FCGR2C alleles
Joris van der Heijden, Willemijn B Breunis, Judy Geissler, et al.
Immunology Letters
|
April 27, 2017
Mutation characterization and heterodimer analysis of patients with leukocyte adhesion deficiency: Including one novel mutation
Shahram Teimourian, Martin De Boer, Dirk Roos, et al.
Experimental Hematology
|
March 8, 2002
Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations
Dirk Roos, Christof Meischl, Martin de Boer, et al.
Molecular Immunology
|
December 9, 2008
High-throughput analysis of the C4 polymorphism by a combination of MLPA and isotype-specific ELISA's
Diana Wouters, Pauline van Schouwenburg, Anneke van der Horst, et al.
Human Mutation
|
January 31, 2014
Primary immunodeficiency caused by an exonized retroposed gene copy inserted in the CYBB gene
Martin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG
|
July 10, 2002
Decreased redox state in red blood cells from patients with sarcoidosis
Snjezana Rothkrantz-Kos, Marjolein Drent, Herma Vuil, et al.
Clinical and Vaccine Immunology : CVI
|
November 6, 2007
Mannose-binding lectin deficiency facilitates abdominal Candida infections in patients with secondary peritonitis
J W Olivier van Till, Piet W Modderman, Martin de Boer, et al.
Journal of Clinical Immunology
|
February 8, 2018
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A)
Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Clinical Immunology (Orlando, Fla.)
|
August 19, 2008
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patients
Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Page
of 8