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Capucine Picard

Showing results (321-330 of 400) with videos related to

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The Journal of Allergy and Clinical Immunology|October 4, 2023
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndromeOlivier Pellé, Solange Moreno, Myriam Ricarda Lorenz, et al.
Blood|December 2, 2010
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, et al.
The New England Journal of Medicine|October 18, 2013
Deep dermatophytosis and inherited CARD9 deficiencyFanny Lanternier, Saad Pathan, Quentin B Vincent, et al.
Nature Immunology|October 30, 2012
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiencyBertrand Boisson, Emmanuel Laplantine, Carolina Prando, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
Nature Immunology|February 1, 2011
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial diseaseJacinta Bustamante, Andres A Arias, Guillaume Vogt, et al.
Science (New York, N.Y.)|September 18, 2007
TLR3 deficiency in patients with herpes simplex encephalitisShen-Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini, et al.
Science (New York, N.Y.)|March 15, 2003
Pyogenic bacterial infections in humans with IRAK-4 deficiencyCapucine Picard, Anne Puel, Marion Bonnet, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
JCI Insight|April 26, 2019
Hematopoietic stem cell transplant effectively rescues lymphocyte differentiation and function in DOCK8-deficient patientsBethany A Pillay, Danielle T Avery, Joanne M Smart, et al.
Pageof 40

Showing results (321-330 of 400) with videos related to

Sort By:
Pageof 40
The Journal of Allergy and Clinical Immunology|October 4, 2023
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndromeOlivier Pellé, Solange Moreno, Myriam Ricarda Lorenz, et al.
Blood|December 2, 2010
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, et al.
The New England Journal of Medicine|October 18, 2013
Deep dermatophytosis and inherited CARD9 deficiencyFanny Lanternier, Saad Pathan, Quentin B Vincent, et al.
Nature Immunology|October 30, 2012
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiencyBertrand Boisson, Emmanuel Laplantine, Carolina Prando, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
Nature Immunology|February 1, 2011
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial diseaseJacinta Bustamante, Andres A Arias, Guillaume Vogt, et al.
Science (New York, N.Y.)|September 18, 2007
TLR3 deficiency in patients with herpes simplex encephalitisShen-Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini, et al.
Science (New York, N.Y.)|March 15, 2003
Pyogenic bacterial infections in humans with IRAK-4 deficiencyCapucine Picard, Anne Puel, Marion Bonnet, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
JCI Insight|April 26, 2019
Hematopoietic stem cell transplant effectively rescues lymphocyte differentiation and function in DOCK8-deficient patientsBethany A Pillay, Danielle T Avery, Joanne M Smart, et al.
Pageof 40