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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.
Frontiers in Immunology
|
October 12, 2017
Very Early-Onset Inflammatory Manifestations of X-Linked Chronic Granulomatous Disease
Roxane Labrosse, Jane Abou-Diab, Annaliesse Blincoe, et al.
Blood
|
April 15, 2015
Faster T-cell development following gene therapy compared with haploidentical HSCT in the treatment of SCID-X1
Fabien Touzot, Despina Moshous, Rita Creidy, et al.
Human Gene Therapy
|
February 1, 2019
Innovative Curative Treatment of Beta Thalassemia: Cost-Efficacy Analysis of Gene Therapy Versus Allogenic Hematopoietic Stem-Cell Transplantation
Séverine Coquerelle, Mariem Ghardallou, Setti Rais, et al.
The Journal of Allergy and Clinical Immunology
|
February 9, 2016
Hyperinflammation in patients with chronic granulomatous disease leads to impairment of hematopoietic stem cell functions
Maren Weisser, Uta M Demel, Stefan Stein, et al.
The Journal of Experimental Medicine
|
December 25, 2016
Inherited CD70 deficiency in humans reveals a critical role for the CD70-CD27 pathway in immunity to Epstein-Barr virus infection
Kazushi Izawa, Emmanuel Martin, Claire Soudais, et al.
Blood
|
September 13, 2011
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients
Monia Ouederni, Quentin B Vincent, Pierre Frange, et al.
Frontiers in Immunology
|
February 13, 2026
Case Report: Characterization of a RAC2 R68W homozygous activating mutation causing combined immune deficiency
Aléhandra Desjardins, Louis Marois, Ágnes Donkó, et al.
Human Molecular Genetics
|
April 18, 2013
Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability
Tangui Le Guen, Laurent Jullien, Fabien Touzot, et al.
Frontiers in Medicine
|
November 1, 2023
Case report: Success of allogeneic hematopoietic stem cell transplantation for refractory systemic-onset juvenile idiopathic arthritis
Camille Beaufils, Catherine Proulx, Annaliesse Blincoe, et al.
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of 6
Search research articles
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Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
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.
Frontiers in Immunology
|
October 12, 2017
Very Early-Onset Inflammatory Manifestations of X-Linked Chronic Granulomatous Disease
Roxane Labrosse, Jane Abou-Diab, Annaliesse Blincoe, et al.
Blood
|
April 15, 2015
Faster T-cell development following gene therapy compared with haploidentical HSCT in the treatment of SCID-X1
Fabien Touzot, Despina Moshous, Rita Creidy, et al.
Human Gene Therapy
|
February 1, 2019
Innovative Curative Treatment of Beta Thalassemia: Cost-Efficacy Analysis of Gene Therapy Versus Allogenic Hematopoietic Stem-Cell Transplantation
Séverine Coquerelle, Mariem Ghardallou, Setti Rais, et al.
The Journal of Allergy and Clinical Immunology
|
February 9, 2016
Hyperinflammation in patients with chronic granulomatous disease leads to impairment of hematopoietic stem cell functions
Maren Weisser, Uta M Demel, Stefan Stein, et al.
The Journal of Experimental Medicine
|
December 25, 2016
Inherited CD70 deficiency in humans reveals a critical role for the CD70-CD27 pathway in immunity to Epstein-Barr virus infection
Kazushi Izawa, Emmanuel Martin, Claire Soudais, et al.
Blood
|
September 13, 2011
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients
Monia Ouederni, Quentin B Vincent, Pierre Frange, et al.
Frontiers in Immunology
|
February 13, 2026
Case Report: Characterization of a RAC2 R68W homozygous activating mutation causing combined immune deficiency
Aléhandra Desjardins, Louis Marois, Ágnes Donkó, et al.
Human Molecular Genetics
|
April 18, 2013
Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability
Tangui Le Guen, Laurent Jullien, Fabien Touzot, et al.
Frontiers in Medicine
|
November 1, 2023
Case report: Success of allogeneic hematopoietic stem cell transplantation for refractory systemic-onset juvenile idiopathic arthritis
Camille Beaufils, Catherine Proulx, Annaliesse Blincoe, et al.
Page
of 6