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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 years
Mickaël 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 anemia
Maurizio 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) mutation
Aude 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 data
Marie 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 lymphohistiocytosis
Jérôme 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 recombination
Kohsuke Imai, Geir Slupphaug, Wen-I Lee, et al.
The New England Journal of Medicine
|
October 2, 2004
Autoimmune lymphoproliferative syndrome with somatic Fas mutations
Eliska 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 immunodeficiencies
Claire Booth, Jean-Antoine Ribeil, Françoise Audat, et al.
European Journal of Pediatrics
|
April 8, 2006
Kaposi's sarcoma in a child with Wiskott-Aldrich syndrome
Capucine 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 Review
Emmanuel Lafont, Beatriz E Marciano, Nizar Mahlaoui, et al.
Page
of 50
Search research articles
Search
Showing results (241-250 of 493) with videos related to
Sort By:
Page
of 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 years
Mickaël 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 anemia
Maurizio 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) mutation
Aude 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 data
Marie 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 lymphohistiocytosis
Jérôme 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 recombination
Kohsuke Imai, Geir Slupphaug, Wen-I Lee, et al.
The New England Journal of Medicine
|
October 2, 2004
Autoimmune lymphoproliferative syndrome with somatic Fas mutations
Eliska 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 immunodeficiencies
Claire Booth, Jean-Antoine Ribeil, Françoise Audat, et al.
European Journal of Pediatrics
|
April 8, 2006
Kaposi's sarcoma in a child with Wiskott-Aldrich syndrome
Capucine 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 Review
Emmanuel Lafont, Beatriz E Marciano, Nizar Mahlaoui, et al.
Page
of 50