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Hydroxyurea is associated with later onset of acute splenic sequestration crisis in sickle cell disease: Lessons from the European Sickle Cell Disease Cohort—Hydroxyurea (ESCORT‐HU) study.
- Published in:
- American Journal of Hematology, 2024, v. 99, n. 4, p. 555, doi. 10.1002/ajh.27214
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- Publication type:
- Article
Early‐onset reduced bone mineral density in patients with pyruvate kinase deficiency.
- Published in:
- American Journal of Hematology, 2023, v. 98, n. 3, p. E57, doi. 10.1002/ajh.26830
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- Publication type:
- Article
Real‐Life experience with hydroxyurea in patients with sickle cell disease: Results from the prospective ESCORT‐HU cohort study.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 10, p. 1223, doi. 10.1002/ajh.26286
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- Publication type:
- Article
Cardiovascular phenotypes predict clinical outcomes in sickle cell disease: An echocardiography‐based cluster analysis.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 9, p. 1166, doi. 10.1002/ajh.26271
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- Publication type:
- Article
Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 9, p. E318, doi. 10.1002/ajh.26245
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- Publication type:
- Article
Transcranial color‐coded duplex sonography reliably identifies intracranial vasculopathy in adult patients with sickle cell disease.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 8, p. 961, doi. 10.1002/ajh.26215
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- Publication type:
- Article
Hydroxycarbamide decreases the free alpha‐hemoglobin pool in red blood cells of adult patients with sickle cell anemia.
- Published in:
- American Journal of Hematology, 2020, v. 95, n. 11, p. E302, doi. 10.1002/ajh.25947
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- Publication type:
- Article
Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease.
- Published in:
- American Journal of Hematology, 2020, v. 95, n. 11, p. 1235, doi. 10.1002/ajh.25937
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- Publication type:
- Article
Muscle structural, energetic and functional benefits of endurance exercise training in sickle cell disease.
- Published in:
- American Journal of Hematology, 2020, v. 95, n. 11, p. 1257, doi. 10.1002/ajh.25936
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- Publication type:
- Article
Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy.
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- American Journal of Hematology, 2020, v. 95, n. 5, p. 456, doi. 10.1002/ajh.25742
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- Publication type:
- Article
Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.
- Published in:
- American Journal of Hematology, 2019, v. 94, n. 5, p. 522, doi. 10.1002/ajh.25421
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- Publication type:
- Article
A common functional PIEZO1 deletion allele associates with red blood cell density in sickle cell disease patients.
- Published in:
- American Journal of Hematology, 2018, v. 93, n. 11, p. E362, doi. 10.1002/ajh.25245
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- Publication type:
- Article
Transfusion‐related adverse events are decreased in pregnant women with sickle cell disease by a change in policy from systematic transfusion to prophylactic oxygen therapy at home: A retrospective survey by the international sickle cell disease observatory
- Published in:
- American Journal of Hematology, 2018, v. 93, n. 6, p. 794, doi. 10.1002/ajh.25097
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- Publication type:
- Article
Incidence and predictive score for delayed hemolytic transfusion reaction in adult patients with sickle cell disease.
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- American Journal of Hematology, 2017, v. 92, n. 12, p. 1340, doi. 10.1002/ajh.24908
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- Publication type:
- Article
Elevated soluble α-hemoglobin pool in sickle cell anemia.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 10, p. E593, doi. 10.1002/ajh.24835
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- Publication type:
- Article
Delayed hemolytic transfusion reaction in adult sickle-cell disease: presentations, outcomes, and treatments of 99 referral center episodes.
- Published in:
- American Journal of Hematology, 2016, v. 91, n. 10, p. 989, doi. 10.1002/ajh.24460
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- Publication type:
- Article
Pulmonary and cerebral microvasculopathy in a patient with sickle cell disease: A role for dense red blood cells?
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- American Journal of Hematology, 2016, v. 91, n. 9, p. 963, doi. 10.1002/ajh.24413
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- Publication type:
- Article
2015 Clinical trials update in sickle cell anemia.
- Published in:
- American Journal of Hematology, 2015, v. 90, n. 10, p. 934, doi. 10.1002/ajh.24116
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- Publication type:
- Article
Partial dysfunction of Treg activation in sickle cell disease.
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- American Journal of Hematology, 2014, v. 89, n. 3, p. 261, doi. 10.1002/ajh.23629
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- Publication type:
- Article
Sickle-cell disease stroke throughout life: A retrospective study in an adult referral center.
- Published in:
- American Journal of Hematology, 2014, v. 89, n. 3, p. 267, doi. 10.1002/ajh.23625
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- Publication type:
- Article
Flow cytometry analyses reveal association between Lu/BCAM adhesion molecule and osteonecrosis in sickle cell disease.
- Published in:
- American Journal of Hematology, 2014, v. 89, n. 1, p. 115, doi. 10.1002/ajh.23597
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- Publication type:
- Article
Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: Description of seven new G6PD mutants.
- Published in:
- American Journal of Hematology, 2012, v. 87, n. 2, p. 208, doi. 10.1002/ajh.22218
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- Publication type:
- Article
Evaluation of the free αα-hemoglobin pool in red blood cells: A new test providing a scale of ββ-thalassemia severity.
- Published in:
- American Journal of Hematology, 2011, v. 86, n. 2, p. 199, doi. 10.1002/ajh.21918
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- Publication type:
- Article
Genetic reversal of the globin switch concurrently modulates both fetal and sickle hemoglobin and reduces red cell sickling.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40923-5
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- Publication type:
- Article
Lower Muscle and Blood Lactate Accumulation in Sickle Cell Trait Carriers in Response to Short High-Intensity Exercise.
- Published in:
- Nutrients, 2022, v. 14, n. 3, p. 501, doi. 10.3390/nu14030501
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- Publication type:
- Article
Extreme acute anemia in an adult sickle cell disease patient: look at the spleen.
- Published in:
- 2012
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- Publication type:
- Letter
Early intermittent noninvasive ventilation for acute chest syndrome in adults with sickle cell disease: a pilot study.
- Published in:
- Intensive Care Medicine, 2010, v. 36, n. 8, p. 1355, doi. 10.1007/s00134-010-1907-4
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- Publication type:
- Article
Glucose-6-Phosphate Dehydrogenase Deficiency and Homozygous Sickle Cell Disease in Congo.
- Published in:
- Human Heredity, 1998, v. 48, n. 4, p. 192, doi. 10.1159/000022801
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- Publication type:
- Article
Clinical Follow-Up of Hydroxyurea-Treated Adults with Sickle Cell Disease.
- Published in:
- Acta Haematologica, 2011, v. 125, n. 3, p. 145, doi. 10.1159/000322248
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- Publication type:
- Article
Epidemiology and disease burden of sickle cell disease in France: A descriptive study based on a French nationwide claim database.
- Published in:
- PLoS ONE, 2021, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0253986
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- Publication type:
- Article
Hemoglobins in Togolese Newborns: Hb S, Hb C, Hb Bart's, and α-Globin Gene Status.
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- American Journal of Hematology, 1998, v. 59, n. 3, p. 208, doi. 10.1002/(SICI)1096-8652(199811)59:3<208::AID-AJH5>3.0.CO;2-R
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- Publication type:
- Article
Hemoglobin debrousse (β96[FG3]Leu → Pro): A new unstable hemoglobin with twofold increased oxygen affinity.
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- American Journal of Hematology, 1996, v. 51, n. 4, p. 276, doi. 10.1002/(SICI)1096-8652(199604)51:4<276::AID-AJH5>3.0.CO;2-T
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- Publication type:
- Article
Disappearance of Hb F and i antigen during the first year of life.
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- American Journal of Hematology, 1980, v. 9, n. 2, p. 161, doi. 10.1002/ajh.2830090204
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- Publication type:
- Article
Unexpected high frequency of P46L TNFRSF1A allele in sub-Saharan West African populations.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 4, p. 513, doi. 10.1038/sj.ejhg.5201344
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- Publication type:
- Article
High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients.
- Published in:
- 2018
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- Publication type:
- journal article
Anti-HI can cause a severe delayed hemolytic transfusion reaction with hyperhemolysis in sickle cell disease patients.
- Published in:
- 2016
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- Publication type:
- case study
Evidence of benefits from using fresh and cryopreserved blood to transfuse patients with acute sickle cell disease.
- Published in:
- 2016
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- Publication type:
- journal article
Partial C antigen in sickle cell disease patients: clinical relevance and prevention of alloimmunization.
- Published in:
- Transfusion, 2010, v. 50, n. 1, p. 13, doi. 10.1111/j.1537-2995.2009.02382.x
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- Publication type:
- Article
Modeling the public health impact of voxelotor in the management of sickle cell disease in France.
- Published in:
- PLoS ONE, 2023, v. 18, n. 9, p. 1, doi. 10.1371/journal.pone.0291211
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- Publication type:
- Article
Conséquences du traitement par voxelotor sur les profils électrophorétiques et chromatographiques de l'hémoglobine.
- Published in:
- Annales de Biologie Clinique, 2023, v. 81, n. 3, p. 320, doi. 10.1684/abc.2023.1814
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- Publication type:
- Article
Automated RBC Exchange has a greater effect on whole blood viscosity than manual whole blood exchange in adult patients with sickle cell disease.
- Published in:
- Vox Sanguinis, 2020, v. 115, n. 8, p. 722, doi. 10.1111/vox.12990
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- Publication type:
- Article
Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiation.
- Published in:
- British Journal of Haematology, 2001, v. 113, n. 2, p. 500, doi. 10.1046/j.1365-2141.2001.02746.x
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- Publication type:
- Article
Liver transplantation in patients with sickle cell disease: possible but challenging—a cohort study.
- Published in:
- Transplant International, 2020, v. 33, n. 10, p. 1220, doi. 10.1111/tri.13669
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- Publication type:
- Article
Phenotypic differences of CD4<sup>+</sup> T cells in response to red blood cell immunization in transfused sickle cell disease patients.
- Published in:
- European Journal of Immunology, 2015, v. 45, n. 6, p. 1868, doi. 10.1002/eji.201445187
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- Publication type:
- Article
Haemoglobin F (HbF) levels in sickle-cell anaemia patients homozygous for the Bantu haplotype.
- Published in:
- European Journal of Haematology, 1999, v. 63, n. 2, p. 136, doi. 10.1111/j.1600-0609.1999.tb01128.x
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- Publication type:
- Article
Substance use disorder of equimolar oxygen-nitrous oxide mixture in French sickle-cell patients: results of the PHEDRE study.
- Published in:
- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03133-w
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- Publication type:
- Article
Alpha haemoglobin‐stabilising protein concentration in the red blood cells of patients with sickle cell anaemia with and without hydroxycarbamide treatment.
- Published in:
- British Journal of Haematology, 2022, v. 196, n. 1, p. 183, doi. 10.1111/bjh.17728
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- Publication type:
- Article
Impact of pre‐eclampsia on renal outcome in sickle cell disease patients.
- Published in:
- British Journal of Haematology, 2021, v. 194, n. 6, p. 1053, doi. 10.1111/bjh.17606
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- Publication type:
- Article
Whole‐blood CCR7 expression and chemoattraction in red blood cell alloimmunization.
- Published in:
- British Journal of Haematology, 2021, v. 194, n. 2, p. 477, doi. 10.1111/bjh.17480
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- Publication type:
- Article
α‐Haemoglobin pool measurement: a useful biomarker for evaluation of β‐thalassaemia intermedia? – response to Huang and Li.
- Published in:
- 2018
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- Publication type:
- Letter to the Editor