LA THÉRAPIE GÉNIQUE: OU EN EST-ON ? = Gene therapy: where do we stand ?CAVAZZANA-CALVO, Marina.La Revue du praticien (Paris). 2013, Vol 63, Num 4, pp 457-461, issn 0035-2640, 5 p.Article

20 ans de thérapie géniqueCAVAZZANA-CALVO, Marina.Biofutur (Puteaux). 2009, Num 300, pp 47-48, issn 0294-3506, 2 p.Article

Guérir un deficit immunitaire congénital : Déficits ImmunitairesMAHLAOUI, Nizar; CAVAZZANA-CALVO, Marina.La Revue du praticien (Paris). 2007, Vol 57, Num 15, pp 1699-1700, issn 0035-2640, 2 p.Article

Correction of genetic blood defects by gene transfer : Hematopoietic stem cell transplantationCAVAZZANA-CALVO, Marina; HACEIN-BEY-ABINA, Salima.Current opinion in hematology. 2001, Vol 8, Num 6, pp 360-367, issn 1065-6251Article

Les ligands Delta et la niche du développement lymphoïde = Notch ligands Delta and lymphoid development nichesSIX, Emmanuelle; SCHMUTZ, Isabelle André; CAVAZZANA-CALVO, Marina et al.MS. Médecine sciences. 2007, Vol 23, Num 1, pp 21-24, issn 0767-0974, 4 p.Article

Mutagenèse insertionnelle et thérapie génique = Insertional mutagenesis and gene therapyCAVAZZANA-CALVO, Marina; GISSELBRECHT, Sylvie.Hématologie (Montrouge). 2005, Vol 11, Num 3, pp 173-180, issn 1264-7527, 8 p.Article

Thérapie génique du déficit immunitaire combiné sévère lié à l'X: Efficacité et complications = Gene therapy of children with X-linked severe combined immune deficiency: efficiency and complicationsFISCHER, Alain; HAESIN-BEY-ABINA, Salima; CAVAZZANA-CALVO, Marina et al.MS. Médecine sciences. 2004, Vol 20, Num 1, pp 115-117, issn 0767-0974, 3 p.Article

Gene therapy of X-linked severe combined immunodeficiencyHACEIN-BEY-ABINA, Salima; FISCHER, Alain; CAVAZZANA-CALVO, Marina et al.International journal of hematology. 2002, Vol 76, Num 4, pp 295-298, issn 0925-5710, 4 p.Article

Ils vont bien... un an après = One year after, they are okCAVAZZANA-CALVO, Marina; HACEIN-BEY-ABINA, Salima; LE DEIST, Francoise et al.MS. Médecine sciences. 2002, Vol 18, Num 8-9, pp 797-798, issn 0767-0974Article

Medical perspectives of adults and embryonic stem cellsCAVAZZANA-CALVO, Marina; ANDRE-SCHMUTZ, Isabelle; LAGRESLE, Chantal et al.Comptes rendus. Biologies. 2002, Vol 325, Num 10, pp 1053-1058, issn 1631-0691, 6 p.Conference Paper

Bone Marrow Transplantation for Primary Immunodeficiency DiseasesSZABOLCS, Paul; CAVAZZANA-CALVO, Marina; FISCHER, Alain et al.The Pediatric clinics of North America. 2010, Vol 57, Num 1, issn 0031-3955, 207-237, xiv [32 p.]Article

Management options for adenosine deaminase deficiency; proceedings of the EBMT satellite workshop (Hamburg, March 2006)BOOTH, Claire; HERSHFIELD, Mike; NOTARANGELO, Luigi et al.Clinical immunology (Orlando, Fla. Print). 2007, Vol 123, Num 2, pp 139-147, issn 1521-6616, 9 p.Article

Optimization of retroviral gene transfer protocol to maintain the lymphoid potential of progenitor cellsHACEIN-BEY, Salima; GROSS, Fabian; NUSBAUM, Patrick et al.Human gene therapy. 2001, Vol 12, Num 3, pp 291-301, issn 1043-0342Article

Severe combined immunodeficiency. A model disease for molecular immunology and therapyFISCHER, Alain; LE DEIST, Francoise; HACEIN-BEY-ABINA, Salima et al.Immunological reviews. 2005, Vol 203, pp 98-109, issn 0105-2896, 12 p.Article

Occurrence of myelodysplastic syndrome in 2 patients with reticular dysgenesisLAGRESLE-PEYROU, Chantal; NEVEN, Bénédicte; ASNAFI, Vahid et al.Journal of allergy and clinical immunology. 2011, Vol 128, Num 1, pp 230-232, issn 0091-6749, 3 p.Article

Thérapie génique de l'adrénoleucodystrophie liée à l'X par transfert du gène dans les cellules souches hématopoïétiques à l'aide d'un vecteur lentiviral. Discussion = Gene therapy of x-linked adrenoleukodystrophy using hematopoietic stem cells and a lentiviral vector. DiscussionCARTIER, Nathalie; HACEIN-BEY-ABINA, Salima; HAUW, Jean-Jacques et al.Bulletin de l'Académie nationale de médecine. 2010, Vol 194, Num 2, pp 255-268, issn 0001-4079, 14 p.Article

Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy : a balance between efficiency and toxicityLAGRESLE-PEYROU, Chantal; YATES, Frank; LEMERCIER, Brigitte et al.Blood. 2006, Vol 107, Num 1, pp 63-72, issn 0006-4971, 10 p.Article

Gene therapy of RAG-2-/- mice: sustained correction of the immunodeficiencyYATES, Frank; MALASSIS-SERIS, Michèle; CAVAZZANA-CALVO, Marina et al.Blood. 2002, Vol 100, Num 12, pp 3942-3949, issn 0006-4971, 8 p.Article

Dynamics of gene-modified progenitor cells analyzed by tracking retroviral integration sites in a human SCID-X1 gene therapy trialWANG, Gary P; BERRY, Charles C; MALANI, Nirav et al.Blood. 2010, Vol 115, Num 22, pp 4356-4366, issn 0006-4971, 11 p.Article

Efficacy of Gene Therapy for X-Linked Severe Combined ImmunodeficiencyHACEIN-BEY-ABINA, Salima; HAUER, Julia; LEIVA, Lily et al.The New England journal of medicine. 2010, Vol 363, Num 4, pp 355-364, issn 0028-4793, 10 p.Article

Allogeneic Hematopoietic Stem-Cell Transplantation for Leukocyte Adhesion DeficiencyQASIM, Waseem; CAVAZZANA-CALVO, Marina; GENNERY, Andrew et al.Pediatrics (Evanston). 2009, Vol 123, Num 3, pp 836-840, issn 0031-4005, 5 p.Article

Evaluation of an algorithm based on peripheral blood hematopoietic progenitor cell and CD34+ cell concentrations to optimize peripheral blood progenitor cell collection by apheresisLEFRERE, Francois; ZOHAR, Sarah; MCINTYRE, Elizabeth et al.Transfusion (Philadelphia, PA). 2007, Vol 47, Num 10, pp 1851-1857, issn 0041-1132, 7 p.Article

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 phenotypeCAVAZZANA-CALVO, Marina; CARLIER, Frédérique; CHEYNIER, Rémi et al.Blood. 2007, Vol 109, Num 10, pp 4575-4581, issn 0006-4971, 7 p.Article

A double-blind low dose-finding phase II study of granulocyte colony-stimulating factor combined with chemotherapy for stem cell mobilization in patients with non-Hodgkin's lymphomaLEFRERE, Francois; ZOHAR, Sarah; CAVAZZANA-CALVO, Marina et al.Haematologica (Roma). 2006, Vol 91, Num 4, pp 550-553, issn 0390-6078, 4 p.Article

Long-term outcome following hematopoietic stem-cell transplantation in Wiskott-Aldrich syndrome : collaborative study of the European Society for Immunodeficiencies and European Group for Blood and Marrow TransplantationOZSAHIN, Hulya; CAVAZZANA-CALVO, Marina; FASTH, Anders et al.Blood. 2008, Vol 111, Num 1, pp 439-445, issn 0006-4971, 7 p.Article