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Capucine Picard

Showing results (361-370 of 400) with videos related to

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The Journal of Allergy and Clinical Immunology|September 24, 2016
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysisCarsten Speckmann, Sam Doerken, Alessandro Aiuti, et al.
Science (New York, N.Y.)|August 2, 2008
Pyogenic bacterial infections in humans with MyD88 deficiencyHorst von Bernuth, Capucine Picard, Zhongbo Jin, et al.
Nature Genetics|January 11, 2011
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signatureTracy A Briggs, Gillian I Rice, Sarah Daly, et al.
The Journal of Allergy and Clinical Immunology|June 13, 2020
Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencingMathieu Fusaro, Jérémie Rosain, Virginie Grandin, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Science (New York, N.Y.)|October 19, 2013
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damageIvan Angulo, Oscar Vadas, Fabien Garçon, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|November 5, 2013
Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiencyMonia Ouederni, Ozden Sanal, Aydan Ikinciogullari, et al.
The Journal of Allergy and Clinical Immunology|April 6, 2015
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunityAnne-Laure Mathieu, Estelle Verronese, Gillian I Rice, et al.
Nature Communications|October 22, 2020
Early-onset autoimmunity associated with SOCS1 haploinsufficiencyJérôme Hadjadj, Carla Noemi Castro, Maud Tusseau, et al.
The Journal of Clinical Investigation|April 18, 2017
Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiencyJulien Cottineau, Molly C Kottemann, Francis P Lach, et al.
Pageof 40

Showing results (361-370 of 400) with videos related to

Sort By:
Pageof 40
The Journal of Allergy and Clinical Immunology|September 24, 2016
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysisCarsten Speckmann, Sam Doerken, Alessandro Aiuti, et al.
Science (New York, N.Y.)|August 2, 2008
Pyogenic bacterial infections in humans with MyD88 deficiencyHorst von Bernuth, Capucine Picard, Zhongbo Jin, et al.
Nature Genetics|January 11, 2011
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signatureTracy A Briggs, Gillian I Rice, Sarah Daly, et al.
The Journal of Allergy and Clinical Immunology|June 13, 2020
Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencingMathieu Fusaro, Jérémie Rosain, Virginie Grandin, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Science (New York, N.Y.)|October 19, 2013
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damageIvan Angulo, Oscar Vadas, Fabien Garçon, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|November 5, 2013
Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiencyMonia Ouederni, Ozden Sanal, Aydan Ikinciogullari, et al.
The Journal of Allergy and Clinical Immunology|April 6, 2015
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunityAnne-Laure Mathieu, Estelle Verronese, Gillian I Rice, et al.
Nature Communications|October 22, 2020
Early-onset autoimmunity associated with SOCS1 haploinsufficiencyJérôme Hadjadj, Carla Noemi Castro, Maud Tusseau, et al.
The Journal of Clinical Investigation|April 18, 2017
Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiencyJulien Cottineau, Molly C Kottemann, Francis P Lach, et al.
Pageof 40