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Erythrocyte autoantibodies in paediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics and significance.
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- British Journal of Haematology, 1999, v. 104, n. 1, p. 189, doi. 10.1046/j.1365-2141.1999.01127.x
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- Article
Sickle cell disease in children: Progress at hand.
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- Patient Care (Print), 1998, v. 32, n. 17, p. 102
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- Article
Parvovirus B19: How serious are the risks?
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- Patient Care (Print), 1997, v. 31, n. 9, p. 155
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- Article
Automated Oxygen Gradient Ektacytometry: A Novel Biomarker in Sickle Cell Anemia.
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- Frontiers in Physiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphys.2021.636609
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- Article
In vitro modeling of the microvascular occlusion and thrombosis that occur in hematologic diseases using microfluidic technology.
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- Journal of Clinical Investigation, 2012, v. 122, n. 1, p. 408, doi. 10.1172/JCI58753
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- Article
β‐Thalassemia pathogenic variants in a cohort of children from the East African coast.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1294
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- Article
A pharmacokinetic–pharmacodynamic analysis of l‐glutamine for the treatment of sickle cell disease: Implications for understanding the mechanism of action and evaluating response to therapy.
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- British Journal of Haematology, 2024, v. 205, n. 3, p. 1147, doi. 10.1111/bjh.19632
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- Article
The bold promise of gene therapy for sickle cell disease.
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- British Journal of Haematology, 2024, v. 204, n. 2, p. 381, doi. 10.1111/bjh.19296
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- Article
Screening for haemoglobin disorders: One size may not fit all.
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- British Journal of Haematology, 2024, v. 204, n. 1, p. 26, doi. 10.1111/bjh.19160
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- Article
Genome‐wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci.
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- British Journal of Haematology, 2023, v. 201, n. 2, p. 343, doi. 10.1111/bjh.18637
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- Article
Hydroxycarbamide treatment reduces transcranial Doppler velocity in the absence of transfusion support in children with sickle cell anaemia, elevated transcranial Doppler velocity, and cerebral vasculopathy: the EXTEND trial.
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- British Journal of Haematology, 2021, v. 195, n. 4, p. 612, doi. 10.1111/bjh.17698
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- Article
Knowledge gaps in reproductive and sexual health in girls and women with sickle cell disease.
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- British Journal of Haematology, 2021, v. 194, n. 6, p. 970, doi. 10.1111/bjh.17658
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- Article
Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics‐guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia.
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- British Journal of Haematology, 2021, v. 194, n. 3, p. 617, doi. 10.1111/bjh.17663
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- Article
Absence of hydroxyurea‐induced mutational effects supports higher utilisation for the treatment of sickle cell anaemia.
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- British Journal of Haematology, 2021, v. 194, n. 2, p. 252, doi. 10.1111/bjh.17323
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- Article
Sickle cell screening in Europe: the time has come.
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- British Journal of Haematology, 2018, v. 183, n. 4, p. 534, doi. 10.1111/bjh.15596
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- Article
Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutrition.
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- British Journal of Haematology, 2018, v. 181, n. 2, p. 242, doi. 10.1111/bjh.15162
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- Article
Hydroxycarbamide treatment and brain MRI/MRA findings in children with sickle cell anaemia.
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- British Journal of Haematology, 2016, v. 175, n. 2, p. 331, doi. 10.1111/bjh.14235
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- Article
Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial.
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- British Journal of Haematology, 2016, v. 172, n. 1, p. 122, doi. 10.1111/bjh.13791
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- Article
Therapeutic phlebotomy is safe in children with sickle cell anaemia and can be effective treatment for transfusional iron overload.
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- British Journal of Haematology, 2015, v. 169, n. 2, p. 262, doi. 10.1111/bjh.13280
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- Article
Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger?Huët anomaly).
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- Nature Genetics, 2002, v. 31, n. 4, p. 410, doi. 10.1038/ng925
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- Article
AnemoCheck-LRS: an optimized, color-based point-of-care test to identify severe anemia in limited-resource settings.
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- 2020
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- Publication type:
- journal article
Reducing transfusion utilization for children with sickle cell anemia in sub‐Saharan Africa with hydroxyurea: Analysis from the phase I/II REACH trial.
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- American Journal of Hematology, 2024, v. 99, n. 4, p. 625, doi. 10.1002/ajh.27244
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- Article
Surveillance for sickle cell disease, United Republic of Tanzania.
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- Bulletin of the World Health Organization, 2020, v. 98, n. 12, p. 859, doi. 10.2471/BLT.20.253583
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- Article
Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110740
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- Article
Prospective identification of variables as outcomes for treatment (PIVOT): study protocol for a randomised, placebo-controlled trial of hydroxyurea for Ghanaian children and adults with haemoglobin SC disease.
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- Trials, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13063-023-07649-7
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- Article
Prospective identification of variables as outcomes for treatment (PIVOT): study protocol for a randomised, placebo-controlled trial of hydroxyurea for Ghanaian children and adults with haemoglobin SC disease.
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- Trials, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13063-023-07649-7
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- Article
Trends in sickle cell trait and disease screening in the Republic of Uganda, 2014–2019.
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- Tropical Medicine & International Health, 2021, v. 26, n. 1, p. 23, doi. 10.1111/tmi.13506
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- Article
Simultaneous point-of-care detection of anemia and sickle cell disease in Tanzania: the RAPID study.
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- 2018
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- journal article
Lack of hydroxyurea‐associated mutagenesis in pediatric sickle cell disease patients.
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- Environmental & Molecular Mutagenesis, 2023, v. 64, n. 3, p. 167, doi. 10.1002/em.22536
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- Article
Effects of Combined UDP-Glucuronosyltransferase (UGT) 1A1*28 and 1A6*2 on Paracetamol Pharmacokinetics in β-Thalassemia/HbE.
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- Pharmacology, 2007, v. 79, n. 2, p. 97, doi. 10.1159/000097908
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- Article
Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.
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- 2002
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- journal article
Model‐based dosing with concentration feedback as an integral part of personalized hydroxycarbamide management.
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- British Journal of Clinical Pharmacology, 2018, v. 84, n. 7, p. 1410, doi. 10.1111/bcp.13585
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- Article
Development of a pharmacokinetic-guided dose individualization strategy for hydroxyurea treatment in children with sickle cell anaemia.
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- British Journal of Clinical Pharmacology, 2016, v. 81, n. 4, p. 742, doi. 10.1111/bcp.12851
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- Article
Seroprevalence of SARS-CoV-2 infection in Cincinnati Ohio USA from August to December 2020.
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- PLoS ONE, 2021, v. 16, n. 7, p. 1, doi. 10.1371/journal.pone.0254667
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- Article
Short Stature in Children with Sickle Cell Anemia Correlates with Alterations in the IGF-I Axis.
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- Journal of Pediatric Endocrinology & Metabolism, 2007, v. 20, n. 2, p. 211
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- Article
EXpanding Treatment for Existing Neurological Disease (EXTEND): An Open-Label Phase II Clinical Trial of Hydroxyurea Treatment in Sickle Cell Anemia.
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- Journal of Medical Internet Research, 2016, v. 18, n. 9, p. 18, doi. 10.2196/resprot.5872
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- Article
Predictors of splenic function preservation in children with sickle cell anemia treated with hydroxyurea.
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- European Journal of Haematology, 2014, v. 93, n. 5, p. 377, doi. 10.1111/ejh.12361
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- Article
Patterns of liver iron accumulation in patients with sickle cell disease and thalassemia with iron overload.
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- European Journal of Haematology, 2010, v. 85, n. 1, p. 51, doi. 10.1111/j.1600-0609.2010.01449.x
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- Article
Asymmetrical Closure of Epiphyses in a Patient with Sickle Cell Anemia.
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- Journal of Pediatric Endocrinology & Metabolism, 2002, v. 15, n. 8, p. 1207
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- Article
Delayed development of sensorineural hearing loss after neonatal hyperbilirubinemia: a case report with brain magnetic resonance imaging.
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- 1996
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- Publication type:
- journal article
Stable-Isotope Dilution HPLC-Electrospray Ionization Tandem Mass Spectrometry Method for Quantifying Hydroxyurea in Dried Blood Samples.
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- Clinical Chemistry, 2016, v. 62, n. 12, p. 1593, doi. 10.1373/clinchem.2016.263715
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- Article
Phenotypic and functional analysis of lymphocytes in paroxysmal nocturnal hemoglobinuria.
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- American Journal of Hematology, 1995, v. 50, n. 4, p. 244, doi. 10.1002/ajh.2830500405
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- Article
Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia.
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- American Journal of Hematology, 1995, v. 50, n. 2, p. 140, doi. 10.1002/ajh.2830500211
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- Article
Hemoglobin sickle-lepore: Report of two siblings and review of the literature.
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- American Journal of Hematology, 1993, v. 44, n. 3, p. 192, doi. 10.1002/ajh.2830440310
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- Article
Transient hypoplastic anemia of childhood.
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- American Journal of Hematology, 1992, v. 40, n. 3, p. 240, doi. 10.1002/ajh.2830400320
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- Article
Transient erythroblastopenia in the first year of life.
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- American Journal of Hematology, 1991, v. 37, n. 3, p. 156, doi. 10.1002/ajh.2830370304
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- Article
Successful Treatment of Refractory Childhood Pemphgus Vulgaris with Anti-CD20 Monoclonal Antibody (Rituximab).
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- Pediatric Dermatology, 2005, v. 22, n. 5, p. 461, doi. 10.1111/j.1525-1470.2005.00118.x
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- Article
Rationale, Development, and Validation of HdxSim, a Clinical Decision Support Tool for Model‐Informed Precision Dosing of Hydroxyurea for Children with Sickle Cell Anemia.
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- Clinical Pharmacology & Therapeutics, 2024, v. 116, n. 3, p. 670, doi. 10.1002/cpt.3119
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- Article
A pharmacokinetic study of paracetamol in Thai β-thalassemia/HbE patients.
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- European Journal of Clinical Pharmacology, 2006, v. 62, n. 9, p. 743, doi. 10.1007/s00228-006-0167-2
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- Publication type:
- Article
Cost-Effectiveness of Hydroxyurea for Sickle Cell Anemia in a Low-Income African Setting: A Model-Based Evaluation of Two Dosing Regimens.
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- PharmacoEconomics, 2023, v. 41, n. 12, p. 1603, doi. 10.1007/s40273-023-01294-3
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- Article