Abstract
David C. Rees, Valentine Brousse, Mariane de Montalembert, Bart J. Biemond, Lucia De Franceschi, Eugene Oteng‐Ntim, Pagona Flevari, Valeria Pinto, John James, Elena Cela, Stefan Eber, Rachel Kesse‐Adu, Jennifer Knight‐Madden, France Pirenne, Aline Santin, Andreas Birkedal Glenthøj
Abstract
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Global, regional, and national prevalence and mortality burden of sickle cell disease, 2000−2021: a systematic analysis from the Global Burden of Disease Study 2021
10.1016/s2352-3026(23)00118-7 · 2023
Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology Commission
10.1016/s2352-3026(23)00096-0 · 2023
Global burden of sickle cell anaemia in children under five, 2010‐2050: modelling based on demographics, excess mortality, and interventions
10.1371/journal.pmed.1001484 · 2013
Sickle cell disease
10.1016/s0140-6736(17)30193-9 · 2017
The clinical spectrum of HbSC sickle cell disease‐not a benign condition
10.1111/bjh.19523 · 2024
The paradox of hemoglobin SC disease
10.1016/s0268-960x(03)00003-1 · 2003
The clinical significance of K‐Cl cotransport activity in red cells of patients with HbSC disease
10.3324/haematol.2014.120402 · 2015
Males with sickle cell disease have higher risks of cerebrovascular disease, increased inflammation, and a reduced response to hydroxyurea
10.1002/ajh.27074 · 2023
Decreased median survival of adults with sickle cell disease after adjusting for left truncation bias: a pooled analysis
10.1182/blood-2018-10-880575 · 2019
AGREE II: advancing guideline development, reporting and evaluation in health care
10.1503/cmaj.090449 · 2010
Significant haemoglobinopathies: a guideline for screening and diagnosis: a British Society for Haematology Guideline
10.1111/bjh.18794 · 2023
The Danish national haemoglobinopathy screening programme: report from 16 years of screening in a low‐prevalence, non‐endemic region
10.1111/bjh.19103 · 2024
Sickle cell anemia in Cuba: prevention and management, 1982‐2018
2019
Parents' experiences of universal screening for haemoglobin disorders: implications for practice in a new genetics era
10.3399/bjgp08x277276 · 2008
Genetic carrier screening for cystic fibrosis, Fragile X Syndrome, hemoglobinopathies, and spinal muscular atrophy
2021
EHA recommendations for preconceptual and antenatal screening and prenatal diagnosis for hemoglobinopathies
10.1002/hem3.70381 · 2026
Recommendations for preconceptual and antenatal screening and prenatal diagnosis for hemoglobinopathies
10.1002/hem3.70381 · 2026
Prenatal genetic counseling in cross‐cultural medicine: a framework for family physicians
2010
Who counsels parents of newborns who are carriers of sickle cell anemia or cystic fibrosis?
10.1007/s10897-012-9537-3 · 2013
Point‐of‐care diagnostic test accuracy in children and adolescents with sickle cell disease: a systematic review and meta‐analysis
10.1016/j.blre.2024.101243 · 2025
Risk of miscarriage following amniocentesis or chorionic villus sampling: systematic review of literature and updated meta‐analysis
10.1002/uog.20353 · 2019
Non‐invasive prenatal testing for the diagnosis of sickle cell disease in high‐risk pregnancies: a systematic review and statistical summary of the current literature
10.1016/j.ejogrb.2025.114799 · 2026
Knowledge insufficient: the management of haemoglobin SC disease
10.1111/bjh.14444 · 2017
Seeing haemoglobin SC: challenging the misperceptions
10.1111/bjh.19580 · 2024
Perceptions of patients and stakeholders on a prenatal sickle cell disease screening and its results among tribal populations of Gujarat: a participatory mixed‐method research
10.1007/s12687-025-00768-5 · 2025
Sickle cell retinopathy: improving care with a multidisciplinary approach
10.2147/jmdh.s90630 · 2017
Natural history and rate of progression of retinopathy in adult patients with sickle cell disease: an 11‐year follow‐up study
10.1182/bloodadvances.2022009147 · 2023
Rétinopathie drépanocytaire: analyse rétrospective portant sur 730 patients suivis dans un centre de référence
Kept as external metadata until matched
Impaired blood rheology plays a role in the chronic disorders associated with sickle cell‐hemoglobin C disease
10.3324/haematol.2014.104745 · 2014
Clinical and laboratory risk factors for sickle cell retinopathy and maculopathy: a scoping review of the current evidence
10.3324/haematol.2024.286420 · 2025
Anti‐vascular endothelial growth factor therapy for stages 3 and 4 proliferative sickle cell retinopathy results in improved anatomical and visual outcomes
10.1097/iae.0000000000004658 · 2026
Central nervous system complications and management in sickle cell disease
10.1182/blood-2015-09-618579 · 2016
Neuropsychologic performance in school‐aged children with sickle cell disease: a report from the Cooperative Study of Sickle Cell Disease
10.1067/mpd.2001.116935 · 2001
Higher‐than‐expected prevalence of silent cerebral infarcts in children with hemoglobin SC disease
10.1182/blood-2014-10-605964 · 2015
Unusually high prevalence of stroke and cerebral vasculopathy in hemoglobin SC disease: a retrospective single institution study
10.1159/000519360 · 2022
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)
10.3324/haematol.2020.265827 · 2021
Cerebrovascular accidents in sickle cell disease: rates and risk factors
1998
The excess burden of stroke in hospitalized adults with sickle cell disease
10.1002/ajh.21476 · 2009
Transcranial Doppler scanning and the assessment of stroke risk in children with haemoglobin sickle cell disease
10.1136/adc.2007.125799 · 2008
Transcranial Doppler in hemoglobin SC disease
10.1002/pbc.26342 · 2017
A mouse model for hemoglobin SC disease recapitulates characteristic human pathologies
10.1182/bloodadvances.2025016793 · doi-reference
Gene therapy for HbSC disease and other compound heterozygous sickle hemoglobinopathies: a time for inclusion
10.1182/blood.2025029964 · doi-reference
Selecting patients with sickle cell disease for gene addition or gene editing‐based therapeutic approaches: Report on behalf of a joint EHA Specialized Working Group and EBMT Hemoglobinopathies Working Party consensus conference
10.1002/hem3.70089 · doi-reference
Allogeneic hematopoietic stem‐cell transplantation for sickle cell disease
10.1056/nejmoa0904971 · doi-reference
Hematopoietic stem cell transplantation in sickle cell disease: a multidimentional review
10.1177/09636897241246351 · doi-reference
Sickle cell disease: an international survey of results of HLA‐identical sibling hematopoietic stem cell transplantation
10.1182/blood-2016-10-745711 · doi-reference
Allogeneic transplantation for sickle cell disease offers high rates of cure with low incidence of severe chronic GVHD in both children and adults: real world data from 2010‐2021. An analysis of the European Society for Blood and Bone Marrow Transplantation Haemoglobinopathy Registry
10.1182/blood-2024-207944 · doi-reference
Hematopoietic stem cell transplantation in thalassemia and sickle cell disease: report from the European Society for Blood and Bone Marrow Transplantation Hemoglobinopathy Registry: 2000−2017
10.1182/blood-2018-168 · doi-reference
Management of sickle cell disease in pregnancy. A British Society for Haematology Guideline
10.1111/bjh.17671 · doi-reference
Current obstetric outcomes in Jamaican women with sickle hemoglobinopathy—a balance of risks for aspirin?
10.1515/jpm-2023-0378 · doi-reference
Proactive management to improve outcomes of high‐risk pregnancy in people with sickle cell disease
10.1182/hematology.2025000744 · doi-reference
An analysis of risk factors for sensorineural hearing loss in children with sickle cell disease
10.1097/mao.0000000000004674 · doi-reference
Low incidence of COVID‐19 severe complications in a large cohort of children with sickle cell disease: a protective role for basal interferon‐1 activation?
10.3324/haematol.2021.278573 · doi-reference
Bone marrow necrosis and fat embolism syndrome in sickle cell disease: increased susceptibility of patients with non‐SS genotypes and a possible association with human parvovirus B19 infection
10.1016/j.blre.2013.12.002 · doi-reference
Severe parvovirus B19 infection in patients with sickle cell disease hospitalized in intensive care units
10.1182/bloodadvances.2025015947 · doi-reference
A retrospective analysis of the significance of haemoglobin SS and SC in disease outcome in patients with sickle cell disease and dengue fever
10.1016/j.ebiom.2015.07.002 · doi-reference
Dengue in hospitalized children with sickle cell disease: a retrospective cohort study in the French departments of America
10.1016/j.jiph.2019.07.015 · doi-reference
The spleen and sickle cell disease: the sick(led) spleen
10.1111/bjh.12950 · doi-reference
Splenic complications in pediatric sickle cell disease: a retrospective cohort review
10.1002/pbc.31219 · doi-reference
Causes and outcomes of the acute chest syndrome in sickle cell disease
10.1056/nejm200006223422502 · doi-reference
Acute chest syndrome is associated with history of asthma in hemoglobin SC disease
10.1002/pbc.22900 · doi-reference
Beyond IV push: alternative methods for management of acute pain in SCD
10.1182/hematology.2024000585 · doi-reference
Guidelines for the management of the acute painful crisis in sickle cell disease
10.1046/j.1365-2141.2003.04193.x · doi-reference
Iron restricted erythropoiesis under hepcidin mimetic treatment (PN23114) improved disease parameters in a Mouse Model for sickle cell disease
10.1182/blood-2023-182472 · doi-reference
Safety and efficacy of mitapivat in sickle cell disease (RISE UP): results from the phase 2 portion of a global, double‐blind, randomised, placebo‐controlled trial
10.1016/s2352-3026(24)00319-3 · doi-reference
The oral ferroportin inhibitor vamifeport improves hemodynamics in a mouse model of sickle cell disease
10.1182/blood.2021014716 · doi-reference
Emerging therapies in sickle cell disease
10.1111/bjh.16504 · doi-reference
Crizanlizumab for the prevention of pain crises in sickle cell disease
10.1056/nejmoa1611770 · doi-reference
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia
10.1002/hem3.108 · doi-reference
Original research: use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC disease
10.1177/1535370216639737 · doi-reference
Iron restriction is an important treatment of hemoglobin SC disease
10.1002/ajh.24380 · doi-reference
Iron deficiency is associated with reduced levels of inflammation and haemolysis in patients with HbSS and HbSC and reduced clinical admissions in those with HbSC
10.1111/bjh.70262 · doi-reference
Iron deficiency in HbSC disease treated with repetitive phlebotomy is associated with fewer sickle cell disease‐related complications
10.1002/ajh.70045 · doi-reference
Baseline characteristics of Ghanaian children and adults enrolled in PIVOT, a randomised clinical trial of hydroxyurea in HbSC disease in sub‐Saharan Africa
10.1111/bjh.19832 · doi-reference
Effects of hydroxyurea treatment for patients with hemoglobin SC disease
10.1002/ajh.24255 · doi-reference
Hydroxyurea therapy for pediatric patients with hemoglobin SC disease
10.1097/00043426-200106000-00014 · doi-reference
Hydroxyurea treatment of children with hemoglobin SC disease
10.1002/pbc.24283 · doi-reference
Management of sickle cell disease: summary of the 2014 evidence‐based report by expert panel members
10.1001/jama.2014.10517 · doi-reference
A novel mouse model of hemoglobin SC disease reveals mechanisms underlying beneficial effects of hydroxyurea
10.1182/blood.2024028136 · doi-reference
Cellular effects of hydroxyurea in Hb SC disease
10.1046/j.1365-2141.1997.3173132.x · doi-reference