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Journal of Clinical Immunology
|
March 3, 2012
Rare duplication or deletion of exons 6, 7 and 8 in CYBB leading to X-linked chronic granulomatous disease in two patients from different families
Marie José Stasia, Karin van Leeuwen, Martin de Boer, et al.
Clinical and Experimental Immunology
|
July 26, 2021
Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in Turkey
Ismail Yaz, Begum Ozbek, Hacer Neslihan Bildik, et al.
Journal of Clinical & Cellular Immunology
|
May 5, 2015
Two CGD Families with a Hypomorphic Mutation in the Activation Domain of p67<sup>phox</sup>
Dirk Roos, Jaap D van Buul, Anton Tj Tool, et al.
The Journal of Allergy and Clinical Immunology
|
August 6, 2013
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
Mustafa Yavuz Köker, Yıldız Camcıoğlu, Karin van Leeuwen, et al.
The Journal of Allergy and Clinical Immunology
|
June 11, 2016
Proinflammatory cytokine response toward fungi but not bacteria in chronic granulomatous disease
Roel P Gazendam, Annemarie van de Geer, John L van Hamme, et al.
Blood
|
December 31, 2014
C-reactive protein enhances IgG-mediated phagocyte responses and thrombocytopenia
Rick Kapur, Katja M J Heitink-Pollé, Leendert Porcelijn, et al.
Blood
|
February 7, 2004
Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis
Taco W Kuijpers, Nikolai A Maianski, Anton T J Tool, et al.
Plos One
|
July 11, 2013
Extensive variation in gene copy number at the killer immunoglobulin-like receptor locus in humans
Sanne Vendelbosch, Martin de Boer, Remko A T W Gouw, et al.
Blood Cells, Molecules & Diseases
|
February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)
Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Human Mutation
|
June 7, 2017
Hermansky-Pudlak syndrome type 2: Aberrant pre-mRNA splicing and mislocalization of granule proteins in neutrophils
Martin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 146) with videos related to
Sort By:
Page
of 15
Journal of Clinical Immunology
|
March 3, 2012
Rare duplication or deletion of exons 6, 7 and 8 in CYBB leading to X-linked chronic granulomatous disease in two patients from different families
Marie José Stasia, Karin van Leeuwen, Martin de Boer, et al.
Clinical and Experimental Immunology
|
July 26, 2021
Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in Turkey
Ismail Yaz, Begum Ozbek, Hacer Neslihan Bildik, et al.
Journal of Clinical & Cellular Immunology
|
May 5, 2015
Two CGD Families with a Hypomorphic Mutation in the Activation Domain of p67<sup>phox</sup>
Dirk Roos, Jaap D van Buul, Anton Tj Tool, et al.
The Journal of Allergy and Clinical Immunology
|
August 6, 2013
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
Mustafa Yavuz Köker, Yıldız Camcıoğlu, Karin van Leeuwen, et al.
The Journal of Allergy and Clinical Immunology
|
June 11, 2016
Proinflammatory cytokine response toward fungi but not bacteria in chronic granulomatous disease
Roel P Gazendam, Annemarie van de Geer, John L van Hamme, et al.
Blood
|
December 31, 2014
C-reactive protein enhances IgG-mediated phagocyte responses and thrombocytopenia
Rick Kapur, Katja M J Heitink-Pollé, Leendert Porcelijn, et al.
Blood
|
February 7, 2004
Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis
Taco W Kuijpers, Nikolai A Maianski, Anton T J Tool, et al.
Plos One
|
July 11, 2013
Extensive variation in gene copy number at the killer immunoglobulin-like receptor locus in humans
Sanne Vendelbosch, Martin de Boer, Remko A T W Gouw, et al.
Blood Cells, Molecules & Diseases
|
February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)
Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Human Mutation
|
June 7, 2017
Hermansky-Pudlak syndrome type 2: Aberrant pre-mRNA splicing and mislocalization of granule proteins in neutrophils
Martin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Page
of 15