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Martin de Boer

Showing results (31-40 of 74) with videos related to

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Haematologica|January 12, 2019
Defective AP-3-dependent VAMP8 trafficking impairs Weibel-Palade body exocytosis in Hermansky-Pudlak Syndrome type 2 blood outgrowth endothelial cellsEllie Karampini, Maaike Schillemans, Menno Hofman, et al.
Journal of Pediatric Hematology/Oncology|April 28, 2018
Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous DiseaseShahram Teimourian, Faezeh Sazgara, Martin de Boer, et al.
The Pediatric Infectious Disease Journal|May 29, 2010
Rhizopus oryzae skin infection treated with posaconazole in a boy with chronic granulomatous diseaseJoanne G Wildenbeest, Matthijs W Oomen, Roger J Brüggemann, et al.
Blood|September 11, 2007
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpuraWillemijn B Breunis, Edwin van Mirre, Marrie Bruin, et al.
Journal of Clinical Immunology|November 25, 2018
Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian PatientsManasi Kulkarni, Gouri Hule, Martin de Boer, et al.
Human Mutation|September 15, 2006
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidaseDirk Roos, Martin de Boer, M Yavuz Köker, et al.
Journal of Clinical Immunology|August 10, 2018
p47<sup>phox-/-</sup> Chronic Granulomatous Disease Patient with Incomplete Kawasaki DiseaseGouri P Hule, Purva R Kanvinde, Manasi A Kulkarni, et al.
Human Mutation|March 25, 2009
Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2BWillemijn B Breunis, Edwin van Mirre, Judy Geissler, et al.
Molecular Immunology|November 26, 2009
Complement factor 7 gene mutations in relation to meningococcal infection and clinical recurrence of meningococcal diseaseTaco W Kuijpers, Melanie Nguyen, Carla Th P Hopman, et al.
Journal of Clinical Immunology|February 25, 2021
Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe ExperienceHalil Tuna Akar, Saliha Esenboga, Deniz Cagdas, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Haematologica|January 12, 2019
Defective AP-3-dependent VAMP8 trafficking impairs Weibel-Palade body exocytosis in Hermansky-Pudlak Syndrome type 2 blood outgrowth endothelial cellsEllie Karampini, Maaike Schillemans, Menno Hofman, et al.
Journal of Pediatric Hematology/Oncology|April 28, 2018
Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous DiseaseShahram Teimourian, Faezeh Sazgara, Martin de Boer, et al.
The Pediatric Infectious Disease Journal|May 29, 2010
Rhizopus oryzae skin infection treated with posaconazole in a boy with chronic granulomatous diseaseJoanne G Wildenbeest, Matthijs W Oomen, Roger J Brüggemann, et al.
Blood|September 11, 2007
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpuraWillemijn B Breunis, Edwin van Mirre, Marrie Bruin, et al.
Journal of Clinical Immunology|November 25, 2018
Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian PatientsManasi Kulkarni, Gouri Hule, Martin de Boer, et al.
Human Mutation|September 15, 2006
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidaseDirk Roos, Martin de Boer, M Yavuz Köker, et al.
Journal of Clinical Immunology|August 10, 2018
p47<sup>phox-/-</sup> Chronic Granulomatous Disease Patient with Incomplete Kawasaki DiseaseGouri P Hule, Purva R Kanvinde, Manasi A Kulkarni, et al.
Human Mutation|March 25, 2009
Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2BWillemijn B Breunis, Edwin van Mirre, Judy Geissler, et al.
Molecular Immunology|November 26, 2009
Complement factor 7 gene mutations in relation to meningococcal infection and clinical recurrence of meningococcal diseaseTaco W Kuijpers, Melanie Nguyen, Carla Th P Hopman, et al.
Journal of Clinical Immunology|February 25, 2021
Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe ExperienceHalil Tuna Akar, Saliha Esenboga, Deniz Cagdas, et al.
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