Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Karin van Leeuwen

Showing results (1-10 of 48) with videos related to

Pageof 5
Sort By:
Molecular Genetics & Genomic Medicine|August 1, 2019
Activation of cryptic splice sites in three patients with chronic granulomatous diseaseMartin de Boer, Karin van Leeuwen, Mathias Hauri-Hohl, et al.
Biochimica Et Biophysica Acta|May 22, 2013
Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous diseaseAstghik Hayrapetyan, Paula C D Dencher, Karin van Leeuwen, et al.
Journal of Cosmetic Dermatology|March 11, 2020
Recurrent skin abscesses in a female X-linked chronic granulomatous disease carrierBurak Altintas, Deniz Cagdas, Karin van Leeuwen, et al.
Annals of Hematology|January 1, 2013
Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiencyStefan Winkler, Karin van Leeuwen, Martin Deboer, et al.
Journal of Clinical Immunology|July 9, 2020
Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats' Disease and Literature ReviewMahsima Shabani, Roxana Pazouki, Mahmoud Parvin, et al.
Blood Cells, Molecules & Diseases|September 9, 2017
Mutation in an exonic splicing enhancer site causing chronic granulomatous diseaseMartin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Journal of Clinical Immunology|January 17, 2023
A Novel Deletion in FERMT3 Causes LAD-III in a Turkish FamilyNezihe Köker, İhsan Deveci, Karin van Leeuwen, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 8, 2018
Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous diseaseStephanie Harris, Helen Braggins, Karin van Leeuwen, et al.
Journal of Clinical Immunology|May 24, 2011
Two X-linked chronic granulomatous disease patients with unusual NADPH oxidase propertiesBaruch Wolach, Arnon Broides, Tal Zeeli, et al.
Human Mutation|January 31, 2014
Primary immunodeficiency caused by an exonized retroposed gene copy inserted in the CYBB geneMartin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Molecular Genetics & Genomic Medicine|August 1, 2019
Activation of cryptic splice sites in three patients with chronic granulomatous diseaseMartin de Boer, Karin van Leeuwen, Mathias Hauri-Hohl, et al.
Biochimica Et Biophysica Acta|May 22, 2013
Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous diseaseAstghik Hayrapetyan, Paula C D Dencher, Karin van Leeuwen, et al.
Journal of Cosmetic Dermatology|March 11, 2020
Recurrent skin abscesses in a female X-linked chronic granulomatous disease carrierBurak Altintas, Deniz Cagdas, Karin van Leeuwen, et al.
Annals of Hematology|January 1, 2013
Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiencyStefan Winkler, Karin van Leeuwen, Martin Deboer, et al.
Journal of Clinical Immunology|July 9, 2020
Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats' Disease and Literature ReviewMahsima Shabani, Roxana Pazouki, Mahmoud Parvin, et al.
Blood Cells, Molecules & Diseases|September 9, 2017
Mutation in an exonic splicing enhancer site causing chronic granulomatous diseaseMartin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Journal of Clinical Immunology|January 17, 2023
A Novel Deletion in FERMT3 Causes LAD-III in a Turkish FamilyNezihe Köker, İhsan Deveci, Karin van Leeuwen, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 8, 2018
Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous diseaseStephanie Harris, Helen Braggins, Karin van Leeuwen, et al.
Journal of Clinical Immunology|May 24, 2011
Two X-linked chronic granulomatous disease patients with unusual NADPH oxidase propertiesBaruch Wolach, Arnon Broides, Tal Zeeli, et al.
Human Mutation|January 31, 2014
Primary immunodeficiency caused by an exonized retroposed gene copy inserted in the CYBB geneMartin de Boer, Karin van Leeuwen, Judy Geissler, et al.
Pageof 5