Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology Commission
| dc.contributor.author | Piel, Frédéric Bernard | |
| dc.contributor.author | Rees, David C. | |
| dc.contributor.author | DeBaun, Michael R. | |
| dc.contributor.author | Nnodu, Obiageli E. | |
| dc.contributor.author | Ranque-Francois, Brigitte | |
| dc.contributor.author | Thompson, Alexis A. | |
| dc.contributor.author | Ware, Russell E. | |
| dc.contributor.author | Abboud, Miguel Raul | |
| dc.contributor.author | Abraham, Allistair A. | |
| dc.contributor.author | Ambrose, Emmanuela Eusebio | |
| dc.contributor.author | Andemariam, Biree | |
| dc.contributor.author | Colah, Roshan B. | |
| dc.contributor.author | Colombatti, Raffaella | |
| dc.contributor.author | Conran, Nicola | |
| dc.contributor.author | Costa, Fernando Ferreira | |
| dc.contributor.author | Cronin, Robert Michael | |
| dc.contributor.author | de Montalembert, Marianne | |
| dc.contributor.author | Elion, Jacques E. | |
| dc.contributor.author | Esrick, Erica B. | |
| dc.contributor.author | Greenway, Anthea L. | |
| dc.contributor.author | Idris, Ibrahim Musa | |
| dc.contributor.author | Issom, David Zacharie | |
| dc.contributor.author | Jain, Dipty L. | |
| dc.contributor.author | Jordan, Lori Chaffin | |
| dc.contributor.author | Kaplan, Zane S. | |
| dc.contributor.author | King, Allison A. | |
| dc.contributor.author | Lloyd-Puryear, Michele Ann | |
| dc.contributor.author | Oppong, Samuel A. | |
| dc.contributor.author | Sharma, Akshay | |
| dc.contributor.author | Sung, Lillian | |
| dc.contributor.author | Tshilolo, Léon Muepu | |
| dc.contributor.author | Wilkie, Diana J. | |
| dc.contributor.author | Ohene-Frempong, Kwaku O. | |
| dc.contributor.department | Pediatrics and Adolescent Medicine | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T12:11:28Z | |
| dc.date.available | 2025-01-24T12:11:28Z | |
| dc.date.issued | 2023 | |
| dc.identifier.doi | https://doi.org/10.1016/S2352-3026(23)00096-0 | |
| dc.identifier.eid | 2-s2.0-85166442023 | |
| dc.identifier.pmid | 37451304 | |
| dc.identifier.uri | http://hdl.handle.net/10938/32566 | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Ltd | |
| dc.relation.ispartof | The Lancet Haematology | |
| dc.source | Scopus | |
| dc.subject | Anemia, sickle cell | |
| dc.subject | Global health | |
| dc.subject | Hematology | |
| dc.subject | Humans | |
| dc.subject | Aciclovir | |
| dc.subject | Amlodipine | |
| dc.subject | Bch bb694 | |
| dc.subject | Betibeglogene autotemcel | |
| dc.subject | Cefepime | |
| dc.subject | Ceftazidime | |
| dc.subject | Cotrimoxazole | |
| dc.subject | Filgrastim | |
| dc.subject | Fluconazole | |
| dc.subject | Gene therapy agent | |
| dc.subject | Hemoglobin gamma chain | |
| dc.subject | Hydralazine | |
| dc.subject | Hydroxyurea | |
| dc.subject | Labetalol | |
| dc.subject | Levetiracetam | |
| dc.subject | Magnesium sulfate | |
| dc.subject | Unclassified drug | |
| dc.subject | Vancomycin | |
| dc.subject | Voxelotor | |
| dc.subject | Africa | |
| dc.subject | Allogeneic hematopoietic stem cell transplantation | |
| dc.subject | Blood cell count | |
| dc.subject | Blood transfusion | |
| dc.subject | Bone necrosis | |
| dc.subject | Cell therapy | |
| dc.subject | Cerebrovascular disease | |
| dc.subject | Chronic pain | |
| dc.subject | Clinical evaluation | |
| dc.subject | Cognitive defect | |
| dc.subject | Comorbidity | |
| dc.subject | Coronavirus disease 2019 | |
| dc.subject | Data analysis | |
| dc.subject | Data base | |
| dc.subject | Data quality | |
| dc.subject | Data quantity | |
| dc.subject | Demographics | |
| dc.subject | Disease severity | |
| dc.subject | Disease surveillance | |
| dc.subject | Economic cost | |
| dc.subject | Education program | |
| dc.subject | Environmental factor | |
| dc.subject | Environmental risk | |
| dc.subject | Erythrocytapheresis | |
| dc.subject | Evidence based practice | |
| dc.subject | Gene addition therapy | |
| dc.subject | Gene editing | |
| dc.subject | Gene therapy | |
| dc.subject | Genetic counseling | |
| dc.subject | Genetic risk factor | |
| dc.subject | Genetic screening | |
| dc.subject | Genetic trait | |
| dc.subject | Geographic mapping | |
| dc.subject | Global disease burden | |
| dc.subject | Gynecologist | |
| dc.subject | Health care access | |
| dc.subject | Health care cost | |
| dc.subject | Health care disparity | |
| dc.subject | Health care financing | |
| dc.subject | Health care personnel | |
| dc.subject | Health care system | |
| dc.subject | High income country | |
| dc.subject | Human | |
| dc.subject | Implementation science | |
| dc.subject | In vivo gene transfer | |
| dc.subject | Infection | |
| dc.subject | Kidney disease | |
| dc.subject | Lancet hematology commission | |
| dc.subject | Leg ulcer | |
| dc.subject | Life expectancy | |
| dc.subject | Medical assessment | |
| dc.subject | Medical service | |
| dc.subject | Medical student | |
| dc.subject | Middle income country | |
| dc.subject | Mortality | |
| dc.subject | Network analysis | |
| dc.subject | Newborn morbidity | |
| dc.subject | Newborn screening | |
| dc.subject | Nursing care | |
| dc.subject | Obstetrics | |
| dc.subject | Outcome assessment | |
| dc.subject | Pandemic | |
| dc.subject | Phase 1 clinical trial (topic) | |
| dc.subject | Phase 2 clinical trial (topic) | |
| dc.subject | Point of care testing | |
| dc.subject | Practice guideline | |
| dc.subject | Prevalence | |
| dc.subject | Priapism | |
| dc.subject | Prospective study | |
| dc.subject | Psychotherapy | |
| dc.subject | Public health insurance | |
| dc.subject | Pulmonary hypertension | |
| dc.subject | Quality control | |
| dc.subject | Review | |
| dc.subject | Risk factor | |
| dc.subject | Sickle cell anemia | |
| dc.subject | Sickle cell crisis | |
| dc.subject | Sociodemographics | |
| dc.subject | Training | |
| dc.subject | Vitreoretinal surgery | |
| dc.title | Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology Commission | |
| dc.type | Review |
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