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Alain Fischer

Showing results (361-370 of 493) with videos related to

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The Journal of Allergy and Clinical Immunology|November 17, 2016
Hematopoietic stem cell transplant in patients with activated PI3K delta syndromeZohreh Nademi, Mary A Slatter, Christopher C Dvorak, et al.
Haematologica|April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)Lucie Heurtier, Hicham Lamrini, Loïc Chentout, 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.
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.
Blood|February 3, 2005
Failure of SCID-X1 gene therapy in older patientsAdrian J Thrasher, Salima Hacein-Bey-Abina, H Bobby Gaspar, et al.
Nature Medicine|June 18, 2021
Retrieval of vector integration sites from cell-free DNADaniela Cesana, Andrea Calabria, Laura Rudilosso, et al.
Blood|March 16, 2013
Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioningJaap Jan Boelens, Mieke Aldenhoven, Duncan Purtill, et al.
The Journal of Allergy and Clinical Immunology|July 30, 2015
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiationTangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, et al.
The Journal of Clinical Investigation|October 3, 2003
A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiencyGilles Courtois, Asma Smahi, Janine Reichenbach, 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.
Pageof 50

Showing results (361-370 of 493) with videos related to

Sort By:
Pageof 50
The Journal of Allergy and Clinical Immunology|November 17, 2016
Hematopoietic stem cell transplant in patients with activated PI3K delta syndromeZohreh Nademi, Mary A Slatter, Christopher C Dvorak, et al.
Haematologica|April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)Lucie Heurtier, Hicham Lamrini, Loïc Chentout, 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.
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.
Blood|February 3, 2005
Failure of SCID-X1 gene therapy in older patientsAdrian J Thrasher, Salima Hacein-Bey-Abina, H Bobby Gaspar, et al.
Nature Medicine|June 18, 2021
Retrieval of vector integration sites from cell-free DNADaniela Cesana, Andrea Calabria, Laura Rudilosso, et al.
Blood|March 16, 2013
Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioningJaap Jan Boelens, Mieke Aldenhoven, Duncan Purtill, et al.
The Journal of Allergy and Clinical Immunology|July 30, 2015
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiationTangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, et al.
The Journal of Clinical Investigation|October 3, 2003
A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiencyGilles Courtois, Asma Smahi, Janine Reichenbach, 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.
Pageof 50