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

Capucine Picard

Showing results (251-260 of 400) with videos related to

Pageof 40
Sort By:
Journal of Clinical Immunology|October 21, 2015
Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015Capucine Picard, Waleed Al-Herz, Aziz Bousfiha, et al.
Plos One|October 27, 2018
Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindredsFabienne Charbit-Henrion, Bernadette Bègue, Anaïs Sierra, et al.
The Journal of Clinical Investigation|November 4, 2009
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cellsMarjorie Côte, Mickaël M Ménager, Agathe Burgess, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|February 27, 2026
An unusual case of RIPK1-related immunodeficiency: The importance of a timely diagnosis for a novel clinical and therapeutic patternAnne-Sophie Parentelli, Anne-Aurélie Lopes, Paul Bastard, et al.
JCI Insight|March 13, 2020
Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutationEmmanuel Martin, Norbert Minet, Anne-Claire Boschat, et al.
Nature Immunology|November 17, 2016
Corrigendum: Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2016
Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) studyVincent Barlogis, Nizar Mahlaoui, Pascal Auquier, et al.
Blood|June 28, 2014
Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patientsBénédicte Neven, Julie Bruneau, Marie-Claude Stolzenberg, et al.
The Journal of Experimental Medicine|May 27, 2015
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasiaBertrand Boisson, Emmanuel Laplantine, Kerry Dobbs, et al.
Journal of Clinical Immunology|May 28, 2013
A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathyLena F Schimke, Nikolaus Rieber, Stacey Rylaarsdam, et al.
Pageof 40

Showing results (251-260 of 400) with videos related to

Sort By:
Pageof 40
Journal of Clinical Immunology|October 21, 2015
Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015Capucine Picard, Waleed Al-Herz, Aziz Bousfiha, et al.
Plos One|October 27, 2018
Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindredsFabienne Charbit-Henrion, Bernadette Bègue, Anaïs Sierra, et al.
The Journal of Clinical Investigation|November 4, 2009
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cellsMarjorie Côte, Mickaël M Ménager, Agathe Burgess, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|February 27, 2026
An unusual case of RIPK1-related immunodeficiency: The importance of a timely diagnosis for a novel clinical and therapeutic patternAnne-Sophie Parentelli, Anne-Aurélie Lopes, Paul Bastard, et al.
JCI Insight|March 13, 2020
Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutationEmmanuel Martin, Norbert Minet, Anne-Claire Boschat, et al.
Nature Immunology|November 17, 2016
Corrigendum: Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2016
Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) studyVincent Barlogis, Nizar Mahlaoui, Pascal Auquier, et al.
Blood|June 28, 2014
Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patientsBénédicte Neven, Julie Bruneau, Marie-Claude Stolzenberg, et al.
The Journal of Experimental Medicine|May 27, 2015
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasiaBertrand Boisson, Emmanuel Laplantine, Kerry Dobbs, et al.
Journal of Clinical Immunology|May 28, 2013
A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathyLena F Schimke, Nikolaus Rieber, Stacey Rylaarsdam, et al.
Pageof 40