Search research articles
Contact Us
Filters
Showing results (271-280 of 493) with videos related to
Page
of 50
Sort By:
Haematologica
|
January 11, 2020
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency
Chantal Lagresle-Peyrou, Aurélien Olichon, Hanem Sadek, et al.
Blood
|
February 3, 2007
Long-term T-cell reconstitution after hematopoietic stem-cell transplantation in primary T-cell-immunodeficient patients is associated with myeloid chimerism and possibly the primary disease phenotype
Marina Cavazzana-Calvo, Frédérique Carlier, Françoise Le Deist, et al.
The Journal of Allergy and Clinical Immunology
|
October 24, 2007
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
Raif S Geha, Luigi D Notarangelo, Jean-Laurent Casanova, et al.
Clinical Immunology (Orlando, Fla.)
|
April 5, 2019
Clinical and economic aspects of newborn screening for severe combined immunodeficiency: DEPISTREC study results
Caroline Thomas, Isabelle Durand-Zaleski, Jérôme Frenkiel, et al.
The American Journal of Gastroenterology
|
April 27, 2011
Defective IL10 signaling defining a subgroup of patients with inflammatory bowel disease
Bernadette Begue, Julien Verdier, Frédéric Rieux-Laucat, et al.
The Journal of Clinical Investigation
|
February 6, 2003
Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis
Despina Moshous, Christophe Pannetier, Régina de Chasseval Rd, et al.
Journal of Clinical Microbiology
|
April 15, 2011
Adenoviral infection presenting as an isolated central nervous system disease without detectable viremia in two children after stem cell transplantation
Pierre Frange, Régis Peffault de Latour, Cécile Arnaud, et al.
Blood
|
May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LG
Stéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Plos One
|
June 28, 2007
Real-time definition of non-randomness in the distribution of genomic events
Ulrich Abel, Annette Deichmann, Cynthia Bartholomae, et al.
Plos One
|
September 7, 2012
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
Amandine Crequer, Capucine Picard, Etienne Patin, et al.
Page
of 50
Search research articles
Search
Showing results (271-280 of 493) with videos related to
Sort By:
Page
of 50
Haematologica
|
January 11, 2020
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency
Chantal Lagresle-Peyrou, Aurélien Olichon, Hanem Sadek, et al.
Blood
|
February 3, 2007
Long-term T-cell reconstitution after hematopoietic stem-cell transplantation in primary T-cell-immunodeficient patients is associated with myeloid chimerism and possibly the primary disease phenotype
Marina Cavazzana-Calvo, Frédérique Carlier, Françoise Le Deist, et al.
The Journal of Allergy and Clinical Immunology
|
October 24, 2007
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
Raif S Geha, Luigi D Notarangelo, Jean-Laurent Casanova, et al.
Clinical Immunology (Orlando, Fla.)
|
April 5, 2019
Clinical and economic aspects of newborn screening for severe combined immunodeficiency: DEPISTREC study results
Caroline Thomas, Isabelle Durand-Zaleski, Jérôme Frenkiel, et al.
The American Journal of Gastroenterology
|
April 27, 2011
Defective IL10 signaling defining a subgroup of patients with inflammatory bowel disease
Bernadette Begue, Julien Verdier, Frédéric Rieux-Laucat, et al.
The Journal of Clinical Investigation
|
February 6, 2003
Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis
Despina Moshous, Christophe Pannetier, Régina de Chasseval Rd, et al.
Journal of Clinical Microbiology
|
April 15, 2011
Adenoviral infection presenting as an isolated central nervous system disease without detectable viremia in two children after stem cell transplantation
Pierre Frange, Régis Peffault de Latour, Cécile Arnaud, et al.
Blood
|
May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LG
Stéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Plos One
|
June 28, 2007
Real-time definition of non-randomness in the distribution of genomic events
Ulrich Abel, Annette Deichmann, Cynthia Bartholomae, et al.
Plos One
|
September 7, 2012
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
Amandine Crequer, Capucine Picard, Etienne Patin, et al.
Page
of 50