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Defining global strategies to improve outcomes in sickle cell disease: a Lancet HaematologyCommission

• Authors : Piel, Frédéric B; Rees, David C; DeBaun, Michael R

• Source: The Lancet Haematology; August 2023, Vol. 10 Issue: 8 pe633-e686, 54p

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Community voices: broadening participation in Science, Technology, Engineering, Mathematics, and Medicine among persons with disabilities.

• Authors : Mattison, Siobhán M.; Gin, Logan; Abraham, Allistair A.

Subjects: PEOPLE with disabilities; COMMUNITIES; EDUCATIONAL change

• Source: Nature Communications; 12/3/2022, Vol. 13 Issue 1, p1-4, 4p

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Expanded HCT-CI Definitions Capture Comorbidity Better for Younger Patients of Allogeneic HCT for Nonmalignant Diseases

• Authors : Broglie, Larisa; Friend, Brian D.; Chhabra, Saurabh

• Source: Transplantation and Cellular Therapy; February 2023, Vol. 29 Issue: 2 p125.e1-125.e9, 9p

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Preservation of Pulmonary Function Following Hematopoietic Cell Transplant for Sickle Cell Disease: A STAR Study

• Authors : Horan, Fiona; Bendiak, Glenda; Abraham, Allistair

• Source: Transplantation and Cellular Therapy; February 2024, Vol. 30 Issue: 2, Number 2 Supplement 1 pS45-S46, 2p

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Reduction in vaso-occlusive events following stem cell transplantation in patients with sickle cell disease

• Authors : Leonard, Alexis; Furstenau, Dana; Abraham, Allistair

• Source: Blood Advances; January 2023, Vol. 7 Issue: 2 p227-234, 8p

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Across the Myeloablative Spectrum: Hematopoietic Cell Transplant Conditioning Regimens for Pediatric Patients with Sickle Cell Disease.

• Authors : Limerick, Emily; Abraham, Allistair

Subjects: SICKLE cell anemia; CHILD patients; AFRICAN AmericansUNITED States

• Source: Journal of Clinical Medicine; Jul2022, Vol. 11 Issue 13, p3856-N.PAG, 11p

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Sickle Cell Transplantation Evaluation of Long-term and Late Effects Registry (STELLAR) to Compare Long-term Outcomes After Hematopoietic Cell Transplantation to Those in Siblings Without Sickle Cell Disease and in Nontransplanted Individuals With Sickle Cell Disease: Design and Feasibility Study

• Authors : Krishnamurti, Lakshmanan; Arnold, Staci D.; Haight, Ann

Subjects: CELL transplantation; SICKLE cell anemia; INTERNET in medicine

• Source: JMIR Research Protocols; Jul2022, Vol. 11 Issue 7, p1-14, 14p

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Survey of Infection Surveillance, Prophylaxis, and Vaccination Practices after Autologous Genetically Modified Cellular Therapies

• Authors : John, Tami; Marón, Gabriela M.; Abraham, Allistair

• Source: Transplantation and Cellular Therapy; February 2024, Vol. 30 Issue: 2, Number 2 Supplement 1 pS235-S235, 1p

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Granulocyte Colony-Stimulating Factor Is Safe and Well Tolerated following Allogeneic Transplantation in Patients with Sickle Cell Disease

• Authors : Shah, Niketa C.; Bhoopatiraju, Sweta; Abraham, Allistair

• Source: Transplantation and Cellular Therapy; March 2022, Vol. 28 Issue: 3 p174.e1-174.e5, 5p

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Low Rates of Cerebral Infarction after Hematopoietic Stem Cell Transplantation in Patients with Sickle Cell Disease at High Risk for Stroke

• Authors : Carpenter, Jessica L.; Nickel, Robert S.; Webb, Jennifer

• Source: Transplantation and Cellular Therapy; December 2021, Vol. 27 Issue: 12 p1018.e1-1018.e9, 9p

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