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Sickle cell disease
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Publications and studies (2099)
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Complementary and alternative medicine for children with sickle cell disease: A systematic review. (2023/05/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Iron chelation therapy. (2023/05/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Hyperammonemia and acute liver failure associated with deferasirox in two adolescents with sickle cell disease. (2023/05/01) ♡
- Determinants of retention in care of newborns diagnosed with sickle cell disease in Liberia: Results from a mixed-methods study of caregivers. (2023/04/04) ♡
- Sickle Cell Disease Diagnosis Uncovered by Incidental Radiograph Findings. (2023/04/01) ♡
- Gene-metabolite annotation with shortest reactional distance enhances metabolite genome-wide association studies results. (2023/03/24) ♡
- Food Consumption of People with Sickle Cell Anemia in a Middle-Income Country. (2023/03/19) ♡
- Orthopaedic Diagnoses in the Black Pediatric Population. (2023/03/15) ♡
- Knowledge and nutrition-related practices among caregivers of adolescents with sickle cell disease in the Greater Accra region of Ghana. (2023/03/06) ♡
- Trends in blood transfusion, hydroxyurea use, and iron overload among children with sickle cell disease enrolled in Medicaid, 2004-2019. (2023/03/01) ♡
- Early splenomegaly and septicaemia in homozygous sickle cell disease: A birth cohort study. (2023/03/01) ♡
- Side effects following COVID-19 vaccination in pediatric patients with sickle cell disease. (2023/03/01) ♡
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Individual-level behavioral interventions to support optimal development of children with sickle cell disease: A systematic review. (2023/03/01) ♡
- Quantitative MRI evaluation of bone marrow in sickle cell disease: relationship with haemolysis and clinical severity. (2023/03/01) ♡
- Palatability and Acceptability of Flaxseed-Supplemented Foods in Children with Sickle Cell Disease. (2023/03/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Intestinal barrier dysfunction in murine sickle cell disease is associated with small intestine neutrophilic inflammation, oxidative stress, and dysbiosis. (2023/02/21) ♡
- Community-level socioeconomic distress is associated with nutritional status in adults with sickle cell anemia. (2023/02/17) ♡
- Red blood cell alloantibodies in paediatric transfusion in sub-Saharan Africa: A new cohort and literature review. (2023/02/09) ♡
- Mineral bone disorders and kidney disease in hospitalized children with sickle cell anemia. (2023/02/02) ♡
- Presentations and outcomes among sickle cell disease patients with COVID-19 at a large southern healthcare system. (2023/02/01) ♡
- HIV-1 Transcription Inhibitor 1E7-03 Decreases Nucleophosmin Phosphorylation. (2023/02/01) ♡
- Enoxaparin adherence for venous thromboembolism prophylaxis in hospitalized patients with sickle cell disease. (2023/02/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Treatment with recombinant ADAMTS13, alleviates hypoxia/reoxygenation-induced pathologies in a mouse model of human sickle cell disease. (2023/02/01) ♡
- Evaluating the implementation of a multi-level mHealth study to improve hydroxyurea utilization in sickle cell disease. (2023/01/20) ♡
- Hybrid effectiveness-implementation trial of guided relaxation and acupuncture for chronic sickle cell disease pain (GRACE): A protocol. (2023/01/18) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. The Pathogenetic Mechanism for Moyamoya Vasculopathy Including a Possible Trigger Effect of Increased Flow Velocity. (2023/01/16) ♡
- Feature preserving mesh network for semantic segmentation of retinal vasculature to support ophthalmic disease analysis. (2023/01/13) ♡
- Development of multi-level standards of care recommendations for sickle cell disease: Experience from SickleInAfrica. (2023/01/12) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Dietary iron restriction protects against vaso-occlusion and organ damage in murine sickle cell disease. (2023/01/12) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Incorporating neglected non-communicable diseases into the national health program-A review. (2023/01/10) ♡
- Inflammatory status in pediatric sickle cell disease: Unravelling the role of immune cell subsets. (2023/01/10) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Clinical genome editing to treat sickle cell disease-A brief update. (2023/01/09) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Rise of the planet of rare anemias: An update on emerging treatment strategies. (2023/01/09) ♡
- Analysis of AVPR1A, thermal and pressure pain thresholds, and stress in sickle cell disease. (2023/01/04) ♡
- Pupil Size and Reactivity in Pediatric Patients With Sickle Cell Disease. (2023/01/01) ♡
- Ethnic-Associated Phenotype Variations in Moyamoya Cerebrovascular Outcomes. (2023/01/01) ♡
- Targeting the von Willebrand Factor-ADAMTS-13 axis in sickle cell disease. (2023/01/01) ♡
- Association of Sickle Cell Disease With Severe Maternal Morbidity. (2023/01/01) ♡
- Gene editing for sickle cell disease and transfusion dependent thalassemias- A cure within reach. (2023/01/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A conservative approach in finding compatible blood for a patient with sickle cell disease having multiple alloantibodies. (2023/01/01) ♡
- 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. (2023/01/01) ♡
- Eligibility Considerations for Female Whole Blood Donors: Hemoglobin Levels and Iron Status in a Nationally Representative Population. (2023/01/01) ♡
- Penicillin Prophylaxis in Patients With Sickle Cell Disease Beyond Age 5 Years. (2023/01/01) ♡
- Newborn screening for sickle cell anemia in Antalya, Türkiye. (2023/01/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Intranasal Sufentanil for Analgesia of Severe Sickle Cell Vaso-occlusive Pain Crisis in the Pediatric (2023-12-26) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. The Predictive Capacity of Machine Learning Models for Progressive Kidney Disease in Individuals With Sickle Cell Anemia (2023-12-14) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. iCanCope With Sickle Cell Pain (2023-12-13) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Defibrotide in Sickle Cell Disease-Related Acute Chest Syndrome (2023-12-08) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. The Role of Endothelin 1 as a Marker of Renal Impairment in Sickle Cell Disease (2023-12-06) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Integration of mHEALTH Into the Care of Patients With Sickle Cell Disease to Increase Hydroxyurea Utilization (2023-11-29) ♡
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