Clinical Outcomes Among Patients With Sickle Cell Disease and Transfusion-Dependent Beta-Thalassemia...
Clinical Outcomes Among Patients With Sickle Cell Disease and Transfusion-Dependent Beta-Thalassemia Treated With Allogeneic Hematopoietic Stem Cell Transplantation: A Systematic Literature Review Clinical Outcomes Among Patients With Sickle Cell Disease and Transfusion-Dependent Beta-Thalassemia Treated With Allogeneic Hematopoietic Stem Cell Transplantation: A Systematic Literature Review
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Dove Medical Press
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English
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Dove Medical Press
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Rajeshwari Nair,1 Nanxin Li,1 Suzan Imren,1 Puja Kohli,1 Krzysztof Lach,2 Lucía Zhu,2 Mirella Dudzic2 1Vertex Pharmaceuticals Incorporated, Boston, MA, USA; 2Maple Health Group LLC, New York, NY, USACorrespondence: Rajeshwari Nair, Vertex Pharmaceuticals Incorporated, 50 Northern Ave, Boston, MA, 02210, USA, Email Rajeshwari_Nair@vrtx.comBackground...
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Clinical Outcomes Among Patients With Sickle Cell Disease and Transfusion-Dependent Beta-Thalassemia Treated With Allogeneic Hematopoietic Stem Cell Transplantation: A Systematic Literature Review Clinical Outcomes Among Patients With Sickle Cell Disease and Transfusion-Dependent Beta-Thalassemia Treated With Allogeneic Hematopoietic Stem Cell Tran...
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TN_cdi_doaj_primary_oai_doaj_org_article_92685cc449a44c82adad32ba1463c382
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_92685cc449a44c82adad32ba1463c382
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1179-2736