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Cancer Immunology, Immunotherapy : CII|December 18, 2008
TNK cells (NKG2D+ CD8+ or CD4+ T lymphocytes) in the control of human tumorsCristina Maccalli, Samantha Scaramuzza, Giorgio ParmianiHuman Gene Therapy|September 7, 2023
Gene Therapy for HemoglobinopathiesMaria Rosa Lidonnici, Samantha Scaramuzza, Giuliana FerrariMolecular Therapy : the Journal of the American Society of Gene Therapy|November 22, 2020
Update on Clinical Ex Vivo Hematopoietic Stem Cell Gene Therapy for Inherited Monogenic DiseasesFrancesca Tucci, Samantha Scaramuzza, Alessandro Aiuti, et al.Journal of Inherited Metabolic Disease|March 13, 2014
Lentiviral vectors for the treatment of primary immunodeficienciesGiada Farinelli, Valentina Capo, Samantha Scaramuzza, et al.Expert Review of Clinical Immunology|May 19, 2010
Current understanding of the Wiskott-Aldrich syndrome and prospects for gene therapySara Trifari, Francesco Marangoni, Samantha Scaramuzza, et al.Human Gene Therapy|March 21, 2006
Efficacy of gene therapy for Wiskott-Aldrich syndrome using a WAS promoter/cDNA-containing lentiviral vector and nonlethal irradiationLoïc Dupré, Francesco Marangoni, Samantha Scaramuzza, et al.Blood|December 12, 2022
Adenine base editor-mediated correction of the common and severe IVS1-110 (G>A) β-thalassemia mutationGiulia Hardouin, Panagiotis Antoniou, Pierre Martinucci, et al.Journal of Immunology (Baltimore, Md. : 1950)|November 4, 2006
Defective Th1 cytokine gene transcription in CD4+ and CD8+ T cells from Wiskott-Aldrich syndrome patientsSara Trifari, Giovanni Sitia, Alessandro Aiuti, et al.Human Gene Therapy|March 17, 2004
Mobilized blood CD34+ cells transduced and selected with a clinically applicable protocol reconstitute lymphopoiesis in SCID-Hu miceSara Deola, Samantha Scaramuzza, Roberto Sciarretta Birolo, et al.Molecular Therapy. Nucleic Acids|April 24, 2023
Novel lentiviral vectors for gene therapy of sickle cell disease combining gene addition and gene silencing strategiesMégane Brusson, Anne Chalumeau, Pierre Martinucci, et al.Pageof 4