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Capucine Picard

Showing results (221-230 of 400) with videos related to

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International Journal of Hematology|May 20, 2018
Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencingShintaro Ono, Manabu Nakayama, Hirokazu Kanegane, et al.
The Journal of Allergy and Clinical Immunology|September 19, 2012
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiencyFabian Hauck, Clotilde Randriamampita, Emmanuel Martin, et al.
Pediatrics|December 14, 2011
Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic reviewSandrine Leroy, Despina Moshous, Olivier Cassar, et al.
British Journal of Haematology|June 9, 2026
Paediatric-onset autoimmune cytopenia: How can we reduce the long-term mortality?Nathalie Aladjidi, Thierry Leblanc, Helder Fernandes, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 20, 2023
Chronic Aichi Virus Infection As a Cause of Long-Lasting Multiorgan Involvement in Patients With Primary Immune DeficienciesJacques Fourgeaud, Mathilde M Lecuit, Philippe Pérot, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|March 4, 2021
Hemophagocytic Lymphohistiocytosis Gene Mutations in Adult Patients Presenting With CLIPPERS-Like SyndromeGuillaume Taieb, Elsa Kaphan, Claire Duflos, et al.
The Journal of Clinical Investigation|August 2, 2012
Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infectionsAmandine Crequer, Anja Troeger, Etienne Patin, et al.
Nature Genetics|February 12, 2008
Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)David Geneviève, Valérie Proulle, Bertrand Isidor, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 23, 2006
IRAK-4 mutation (Q293X): rapid detection and characterization of defective post-transcriptional TLR/IL-1R responses in human myeloid and non-myeloid cellsDonald J Davidson, Andrew J Currie, Dawn M E Bowdish, et al.
Pageof 40

Showing results (221-230 of 400) with videos related to

Sort By:
Pageof 40
International Journal of Hematology|May 20, 2018
Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencingShintaro Ono, Manabu Nakayama, Hirokazu Kanegane, et al.
The Journal of Allergy and Clinical Immunology|September 19, 2012
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiencyFabian Hauck, Clotilde Randriamampita, Emmanuel Martin, et al.
Pediatrics|December 14, 2011
Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic reviewSandrine Leroy, Despina Moshous, Olivier Cassar, et al.
British Journal of Haematology|June 9, 2026
Paediatric-onset autoimmune cytopenia: How can we reduce the long-term mortality?Nathalie Aladjidi, Thierry Leblanc, Helder Fernandes, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 20, 2023
Chronic Aichi Virus Infection As a Cause of Long-Lasting Multiorgan Involvement in Patients With Primary Immune DeficienciesJacques Fourgeaud, Mathilde M Lecuit, Philippe Pérot, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|March 4, 2021
Hemophagocytic Lymphohistiocytosis Gene Mutations in Adult Patients Presenting With CLIPPERS-Like SyndromeGuillaume Taieb, Elsa Kaphan, Claire Duflos, et al.
The Journal of Clinical Investigation|August 2, 2012
Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infectionsAmandine Crequer, Anja Troeger, Etienne Patin, et al.
Nature Genetics|February 12, 2008
Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)David Geneviève, Valérie Proulle, Bertrand Isidor, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 23, 2006
IRAK-4 mutation (Q293X): rapid detection and characterization of defective post-transcriptional TLR/IL-1R responses in human myeloid and non-myeloid cellsDonald J Davidson, Andrew J Currie, Dawn M E Bowdish, et al.
Pageof 40