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

Alain Fischer

Showing results (241-250 of 493) with videos related to

Pageof 50
Sort By:
The Journal of Allergy and Clinical Immunology|January 15, 2022
An appraisal of the frequency and severity of noninfectious manifestations in primary immunodeficiencies: A study of a national retrospective cohort of 1375 patients over 10 yearsMickaël Alligon, Nizar Mahlaoui, Virginie Courteille, et al.
Journal of Pediatric Hematology/Oncology|April 17, 2013
Sirolimus as maintenance treatment in an infant with life-threatening multiresistant pure red cell anemia/autoimmune hemolytic anemiaMaurizio Miano, Vincenzo Poggi, Laura Banov, et al.
The Journal of Allergy and Clinical Immunology|August 4, 2012
Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutationAude Magerus-Chatinet, Marie-Claude Stolzenberg, Nina Lanzarotti, et al.
The Journal of Allergy and Clinical Immunology|April 5, 2015
Systematic neonatal screening for severe combined immunodeficiency and severe T-cell lymphopenia: Analysis of cost-effectiveness based on French real field dataMarie Caroline Clément, Nizar Mahlaoui, Cécile Mignot, et al.
British Journal of Haematology|June 13, 2002
Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosisJérôme Feldmann, Françoise Le Deist, Marie Ouachée-Chardin, et al.
Nature Immunology|September 6, 2003
Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombinationKohsuke Imai, Geir Slupphaug, Wen-I Lee, et al.
The New England Journal of Medicine|October 2, 2004
Autoimmune lymphoproliferative syndrome with somatic Fas mutationsEliska Holzelova, Cédric Vonarbourg, Marie-Claude Stolzenberg, et al.
British Journal of Haematology|October 24, 2006
CD34 stem cell top-ups without conditioning after initial haematopoietic stem cell transplantation for correction of incomplete haematopoietic and immunological recovery in severe congenital immunodeficienciesClaire Booth, Jean-Antoine Ribeil, Françoise Audat, et al.
European Journal of Pediatrics|April 8, 2006
Kaposi's sarcoma in a child with Wiskott-Aldrich syndromeCapucine Picard, Fethi Mellouli, Renan Duprez, et al.
Journal of Clinical Immunology|September 13, 2020
Nocardiosis Associated with Primary Immunodeficiencies (Nocar-DIP): an International Retrospective Study and Literature ReviewEmmanuel Lafont, Beatriz E Marciano, Nizar Mahlaoui, et al.
Pageof 50

Showing results (241-250 of 493) with videos related to

Sort By:
Pageof 50
The Journal of Allergy and Clinical Immunology|January 15, 2022
An appraisal of the frequency and severity of noninfectious manifestations in primary immunodeficiencies: A study of a national retrospective cohort of 1375 patients over 10 yearsMickaël Alligon, Nizar Mahlaoui, Virginie Courteille, et al.
Journal of Pediatric Hematology/Oncology|April 17, 2013
Sirolimus as maintenance treatment in an infant with life-threatening multiresistant pure red cell anemia/autoimmune hemolytic anemiaMaurizio Miano, Vincenzo Poggi, Laura Banov, et al.
The Journal of Allergy and Clinical Immunology|August 4, 2012
Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutationAude Magerus-Chatinet, Marie-Claude Stolzenberg, Nina Lanzarotti, et al.
The Journal of Allergy and Clinical Immunology|April 5, 2015
Systematic neonatal screening for severe combined immunodeficiency and severe T-cell lymphopenia: Analysis of cost-effectiveness based on French real field dataMarie Caroline Clément, Nizar Mahlaoui, Cécile Mignot, et al.
British Journal of Haematology|June 13, 2002
Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosisJérôme Feldmann, Françoise Le Deist, Marie Ouachée-Chardin, et al.
Nature Immunology|September 6, 2003
Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombinationKohsuke Imai, Geir Slupphaug, Wen-I Lee, et al.
The New England Journal of Medicine|October 2, 2004
Autoimmune lymphoproliferative syndrome with somatic Fas mutationsEliska Holzelova, Cédric Vonarbourg, Marie-Claude Stolzenberg, et al.
British Journal of Haematology|October 24, 2006
CD34 stem cell top-ups without conditioning after initial haematopoietic stem cell transplantation for correction of incomplete haematopoietic and immunological recovery in severe congenital immunodeficienciesClaire Booth, Jean-Antoine Ribeil, Françoise Audat, et al.
European Journal of Pediatrics|April 8, 2006
Kaposi's sarcoma in a child with Wiskott-Aldrich syndromeCapucine Picard, Fethi Mellouli, Renan Duprez, et al.
Journal of Clinical Immunology|September 13, 2020
Nocardiosis Associated with Primary Immunodeficiencies (Nocar-DIP): an International Retrospective Study and Literature ReviewEmmanuel Lafont, Beatriz E Marciano, Nizar Mahlaoui, et al.
Pageof 50