Works matching DE "SICKLE cell anemia treatment"
Results: 556
The Direct Medical Costs of Sickle Cell Disease in Saudi Arabia: Insights from a Single Center Study.
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- Healthcare (2227-9032), 2025, v. 13, n. 4, p. 420, doi. 10.3390/healthcare13040420
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Haemoglobin disorders.
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- Eastern Mediterranean Health Journal, 2011, v. 17, n. 9, p. 713
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- Article
The Experience and Health-Related Quality of Life after Haploidentical Stem Cell Transplantation for Adults with Sickle Cell Disease.
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- Western Journal of Nursing Research, 2019, v. 41, n. 12, p. 1829, doi. 10.1177/0193945919870828
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- Article
Pain Frequency and Health Care Utilization Patterns in Women with Sickle Cell Disease Experiencing Menstruation-Associated Pain Crises.
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- Journal of Women's Health (15409996), 2023, v. 32, n. 12, p. 1284, doi. 10.1089/jwh.2023.0023
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Sickle cell disease expenditures and outcomes.
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- Public Health Reports, 1997, v. 112, n. 1, p. 38
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- Article
Similar burden of type 2 diabetes among adult patients with sickle cell disease relative to African Americans in the U.S. population: a six‐year population‐based cohort analysis.
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- Angewandte Chemie, 2019, v. 131, n. 15, p. 116, doi. 10.1111/bjh.15773
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Bittersweet news for the adult sickle cell patient.
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- Angewandte Chemie, 2019, v. 131, n. 15, p. 9, doi. 10.1111/bjh.15771
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- Article
Low urinary levels of angiotensin‐converting enzyme 2 may contribute to albuminuria in children with sickle cell anaemia.
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- Angewandte Chemie, 2019, v. 131, n. 15, p. 190, doi. 10.1111/bjh.15439
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Biallelic BIRC3 inactivation in chronic lymphocytic leukaemia patients with 11q deletion identifies a subgroup with very aggressive disease.
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- Angewandte Chemie, 2019, v. 131, n. 15, p. 156, doi. 10.1111/bjh.15405
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A significant proportion of children of African descent with HbSβ<sup>0</sup> thalassaemia are inaccurately diagnosed based on phenotypic analyses alone.
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- Angewandte Chemie, 2019, v. 131, n. 15, p. 153, doi. 10.1111/bjh.15400
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- Article
Self-efficacy and readiness for transition from pediatric to adult care in sickle cell disease.
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- 2016
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- Publication type:
- journal article
Incidence and management of priapism in sickle cell disease: A study from local hospital at south west Saudi Arabia.
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- Pakistan Journal of Surgery, 2017, v. 33, n. 1, p. 20
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- Article
A Hemoglobin-Based Multifunctional Therapeutic: Polynitroxylated Pegylated Hemoglobin.
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- Artificial Organs, 2012, v. 36, n. 2, p. 215, doi. 10.1111/j.1525-1594.2011.01307.x
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Hemoglobin-Based Blood Substitutes and the Treatment of Sickle Cell Disease: More Harm than Help?
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- Biomolecules (2218-273X), 2017, v. 7, n. 1, p. 2, doi. 10.3390/biom7010002
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Respect, trust, and the management of sickle cell disease pain in hospital: comparative analysis of concern-raising behaviors, preliminary model, and agenda for international collaborative research to inform practice.
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- Ethnicity & Health, 2011, v. 16, n. 4/5, p. 405, doi. 10.1080/13557858.2011.555520
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- Article
Barriers to conceiving sibling donors for sickle cell disease: perspectives from patients and parents.
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- Ethnicity & Health, 2011, v. 16, n. 4/5, p. 431, doi. 10.1080/13557858.2011.558619
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- Article
Informing choice or teaching submission to medical authority: a case study of adolescent transitioning for sickle cell patients.
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- Ethnicity & Health, 2011, v. 16, n. 4/5, p. 313, doi. 10.1080/13557858.2011.553669
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Cognitive–Behavioural Therapy for the Management of Sickle Cell Disease Pain: Identification and Assessment of Costs.
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- Ethnicity & Health, 2001, v. 6, n. 1, p. 59, doi. 10.1080/13557850123965
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Targeted Busulfan therapy with a steady-state concentration of 600-700 ng/mL in patients with sickle cell disease receiving HLA-identical sibling bone marrow transplant.
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- Bone Marrow Transplantation, 2014, v. 49, n. 3, p. 366, doi. 10.1038/bmt.2013.188
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- Article
Hydroxyurea Therapy Mobilises Arachidonic Acid from Inner CellMembrane Aminophospholipids in Patients with Homozygous Sickle Cell Disease.
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- Journal of Lipids, 2011, p. 1, doi. 10.1155/2011/718014
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- Article
CONTRIBUTIONS OF THE SINGULAR THERAPEUTIC PROJECT IN SICKLE CELL ANEMIA IN A REGIONAL HOSPITAL: A CASE REPORT.
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- Journal of Nursing UFPE / Revista de Enfermagem UFPE, 2016, v. 10, n. 7, p. 2650, doi. 10.5205/reuol.9106-80230-1-SM1007201644
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- Article
Sickle cell disease: perspectives on the assistance provided in primary attention.
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- Revista de Pesquisa: Cuidado é Fundamental, 2017, v. 9, n. 3, p. 768, doi. 10.9789/2175-5361.2017.v9i3.768-775
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- Article
Proportion of Adults With Sickle Cell Anemia and Pain Crises Receiving Hydroxyurea.
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- JAMA: Journal of the American Medical Association, 2015, v. 313, n. 16, p. 1671, doi. 10.1001/jama.2015.3075
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Management of Sickle Cell Disease Summary of the 2014 Evidence-Based Report by Expert Panel Members.
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- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 10, p. 1033, doi. 10.1001/jama.2014.10517
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Health Agencies Update.
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- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 8, p. 779
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Nonmyeloablative HLA-Matched Sibling Allogeneic Hematopoietic Stem Cell Transplantation for Severe Sickle Cell Phenotype.
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- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 1, p. 48, doi. 10.1001/jama.2014.7192
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Advances Reshaping Sickle Cell Therapy.
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- JAMA: Journal of the American Medical Association, 2011, v. 305, n. 3, p. 239, doi. 10.1001/jama.2010.1929
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One Small Step for Sickle Cell Disease: Many More to Go.
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- 2021
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- journal article
Kneeling Was the First Step for Sickle Cell Disease.
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- 2021
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- Editorial
Hydroxyurea Increases Plasma Concentrations of Microparticles and Reduces Coagulation Activation and Fibrinolysis in Patients with Sickle Cell Anemia.
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- Acta Haematologica, 2015, v. 133, n. 3, p. 287, doi. 10.1159/000362148
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Two-Year Analysis of Efficacy and Safety of Deferasirox Treatment for Transfusional Iron Overload in Sickle Cell Anemia Patients.
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- Acta Haematologica, 2012, v. 128, n. 2, p. 113, doi. 10.1159/000338560
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- Article
Patient-Reported Outcomes of Deferasirox (Exjade®, ICL670) versus Deferoxamine in Sickle Cell Disease Patients with Transfusional Hemosiderosis.
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- Acta Haematologica, 2008, v. 119, n. 3, p. 133, doi. 10.1159/000125550
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Imaging manifestations of acquired elastopathy resembling pseudoxanthoma elasticum in patients with beta thalassaemia major and sickle cell disease.
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- 2016
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- journal article
Meteorological parameters and hospitalizations of patients with sickle cell anemia: a 20-year retrospective study in Campinas, São Paulo, Brazil.
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- International Journal of Environmental Health Research, 2023, v. 33, n. 12, p. 1430, doi. 10.1080/09603123.2022.2098258
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- Article
A genetic strategy to treat sickle cell anemia by coregulating globin transgene expression and RNA interference.
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- Nature Biotechnology, 2006, v. 24, n. 1, p. 89, doi. 10.1038/nbt1176
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Optimizing Adolescent Transition To Adult Care for Sickle Cell Disease.
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- MEDSURG Nursing, 2013, v. 22, n. 4, p. 255
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Reversible splenial lesion syndrome during venoarterial extracorporeal membrane oxygenation.
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- 2019
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- journal article
Ten tips for managing critically ill patients with sickle cell disease.
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- 2017
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- journal article
Influence of β<sup>S</sup> allele in the lipid peroxidation and antioxidant capacity parameters.
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- International Journal of Laboratory Hematology, 2014, v. 36, n. 2, p. 205, doi. 10.1111/ijlh.12154
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- Article
Automated red cell exchange in sickle cell disease patients: Retrospective analysis of series of cases in a tertiary care hospital in Eastern India.
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- Asian Journal of Transfusion Science, 2024, v. 18, n. 2, p. 350, doi. 10.4103/ajts.ajts_174_21
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Hyperhemolysis syndrome in a case of sickle cell disease.
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- Asian Journal of Transfusion Science, 2024, v. 18, n. 1, p. 155, doi. 10.4103/ajts.ajts_148_21
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- Article
A case report and review of literature on the role of automated red cell exchange in managing sickle cell crisis in India.
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- Asian Journal of Transfusion Science, 2023, v. 17, n. 2, p. 279, doi. 10.4103/ajts.ajts_138_22
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- Article
Comparative study between chronic automated red blood cell exchange and manual exchange transfusion in patients with sickle cell disease: A single center experience from Saudi Arabia.
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- Asian Journal of Transfusion Science, 2023, v. 17, n. 1, p. 91, doi. 10.4103/ajts.ajts_13_21
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A conservative approach in finding compatible blood for a patient with sickle cell disease having multiple alloantibodies.
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- Asian Journal of Transfusion Science, 2023, v. 17, n. 1, p. 121, doi. 10.4103/ajts.ajts_114_22
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The association of transfusion status with antioxidant enzymes and malondialdehyde level in Nigerians with sickle cell disease.
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- Asian Journal of Transfusion Science, 2014, v. 8, n. 1, p. 47, doi. 10.4103/0973-6247.126692
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- Article
Sickle cell disease in southwestern Nigeria: assessment of knowledge of primary health care workers and available facilities.
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- Transactions of the Royal Society of Tropical Medicine & Hygiene, 2018, v. 112, n. 2, p. 81, doi. 10.1093/trstmh/try025
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Sickle-cell disease: a call to action.
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- Transactions of the Royal Society of Tropical Medicine & Hygiene, 2015, v. 109, n. 6, p. 355, doi. 10.1093/trstmh/trv035
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Update on sickle cell disease.
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- British Journal of Hospital Medicine (17508460), 2016, v. 77, n. 4, p. C55, doi. 10.12968/hmed.2016.77.4.C55
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Sickle Cell Disease in Clinical Practice.
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- 2016
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- Book Review
Acute health-care use by patients with sickle cell disease.
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- British Journal of Hospital Medicine (17508460), 2013, v. 74, n. 1, p. 10, doi. 10.12968/hmed.2013.74.1.10b
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- Article