G De Saint Basile - JoVE Visualize

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British Journal of Haematology|July 27, 2005

Transient familial haemophagocytic lymphohistiocytosis reactivation post-CD34 haematopoietic stem cell transplantationH Almousa, M Ouachée-Chardin, C Picard, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001

CD40-CD40L independent Ig gene hypermutation suggests a second B cell diversification pathway in humansS Weller, A Faili, C Garcia, et al.

Blood|April 15, 1996

gamma-c gene transfer into SCID X1 patients' B-cell lines restores normal high-affinity interleukin-2 receptor expression and functionH Hacein-Bey, M Cavazzana-Calvo, F Le Deist, et al.

Science (New York, N.Y.)|December 3, 1999

Perforin gene defects in familial hemophagocytic lymphohistiocytosisS E Stepp, R Dufourcq-Lagelouse, F Le Deist, et al.

Blood|January 29, 2000

Protein truncation test of LYST reveals heterogenous mutations in patients with Chediak-Higashi syndromeS Certain, F Barrat, E Pastural, et al.

Immunogenetics|May 10, 2000

Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group BW Wiszniewski, M C Fondaneche, N Lambert, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 21, 2018

TTC7A mutation must be considered in patients with repeated intestinal atresia associated with early inflammatory bowel disease: Two new case reports and a literature reviewJ Fayard, S Collardeau, Y Bertrand, et al.

Science (New York, N.Y.)|April 28, 2000

Gene therapy of human severe combined immunodeficiency (SCID)-X1 diseaseM Cavazzana-Calvo, S Hacein-Bey, G de Saint Basile, et al.

The Journal of Pediatrics|May 6, 1999

Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: a retrospective survey of 31 patientsP Quartier, M Debré, J De Blic, et al.

Human Molecular Genetics|July 1, 1997

Identification of mutations in two major mRNA isoforms of the Chediak-Higashi syndrome gene in human and mouseM D Barbosa, F J Barrat, V T Tchernev, et al.

Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:

Pageof 9

British Journal of Haematology|July 27, 2005

Transient familial haemophagocytic lymphohistiocytosis reactivation post-CD34 haematopoietic stem cell transplantationH Almousa, M Ouachée-Chardin, C Picard, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001

CD40-CD40L independent Ig gene hypermutation suggests a second B cell diversification pathway in humansS Weller, A Faili, C Garcia, et al.

Blood|April 15, 1996

gamma-c gene transfer into SCID X1 patients' B-cell lines restores normal high-affinity interleukin-2 receptor expression and functionH Hacein-Bey, M Cavazzana-Calvo, F Le Deist, et al.

Science (New York, N.Y.)|December 3, 1999

Perforin gene defects in familial hemophagocytic lymphohistiocytosisS E Stepp, R Dufourcq-Lagelouse, F Le Deist, et al.

Blood|January 29, 2000

Protein truncation test of LYST reveals heterogenous mutations in patients with Chediak-Higashi syndromeS Certain, F Barrat, E Pastural, et al.

Immunogenetics|May 10, 2000

Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group BW Wiszniewski, M C Fondaneche, N Lambert, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 21, 2018

TTC7A mutation must be considered in patients with repeated intestinal atresia associated with early inflammatory bowel disease: Two new case reports and a literature reviewJ Fayard, S Collardeau, Y Bertrand, et al.

Science (New York, N.Y.)|April 28, 2000

Gene therapy of human severe combined immunodeficiency (SCID)-X1 diseaseM Cavazzana-Calvo, S Hacein-Bey, G de Saint Basile, et al.

The Journal of Pediatrics|May 6, 1999

Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: a retrospective survey of 31 patientsP Quartier, M Debré, J De Blic, et al.

Human Molecular Genetics|July 1, 1997

Identification of mutations in two major mRNA isoforms of the Chediak-Higashi syndrome gene in human and mouseM D Barbosa, F J Barrat, V T Tchernev, et al.

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