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Blood|December 14, 2002
A novel murine model of Cooley anemia and its rescue by lentiviral-mediated human beta-globin gene transferStefano Rivella, Chad May, Amy Chadburn, et al.Cell|January 28, 2017
A Red Carpet for Iron MetabolismMartina U Muckenthaler, Stefano Rivella, Matthias W Hentze, et al.Best Practice & Research. Clinical Haematology|October 23, 2004
Globin gene transfer for treatment of the beta-thalassemias and sickle cell diseaseMichel Sadelain, Stefano Rivella, Leszek Lisowski, et al.Hematology/Oncology Clinics of North America|February 21, 2018
Emerging TherapiesAmaliris Guerra, Khaled M Musallam, Ali T Taher, et al.Haematologica|June 5, 2013
Non-transfusion-dependent thalassemiasKhaled M Musallam, Stefano Rivella, Elliott Vichinsky, et al.Hematology/Oncology Clinics of North America|February 21, 2018
Ineffective Erythropoiesis: Anemia and Iron OverloadRitama Gupta, Khaled M Musallam, Ali T Taher, et al.The American Journal of Pathology|August 4, 2020
Heparanase Level and Procoagulant Activity Are Increased in Thalassemia and Attenuated by Janus Kinase 2 InhibitionHussam Ghoti, Shanny Ackerman, Stefano Rivella, et al.Antioxidants & Redox Signaling|November 24, 2020
The Role of Iron in Benign and Malignant HematopoiesisSayantani Sinha, Joana Pereira-Reis, Amaliris Guerra, et al.Hematology/Oncology Clinics of North America|March 12, 2023
Pathogenic Mechanisms in Thalassemia I: Ineffective Erythropoiesis and HypercoagulabilityRayan Bou-Fakhredin, Stefano Rivella, Maria Domenica Cappellini, et al.Annals of the New York Academy of Sciences|December 13, 2005
Progress toward the genetic treatment of the beta-thalassemiasMichel Sadelain, Leszek Lisowski, Selda Samakoglu, et al.Pageof 13