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"Severity" in adult sickle cell disease.
- Published in:
- American Journal of Hematology, 2023, v. 98, n. 10, p. 1508, doi. 10.1002/ajh.27024
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- Article
An integrated therapeutic approach to sickle cell disease management beyond infancy.
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- American Journal of Hematology, 2023, v. 98, n. 7, p. 1087, doi. 10.1002/ajh.26956
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- Article
Fetal hemoglobin per erythrocyte (HbF/F‐cell) after gene therapy for sickle cell anemia.
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- American Journal of Hematology, 2023, v. 98, n. 2, p. E32, doi. 10.1002/ajh.26791
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- Article
HbSC disease: A time for progress.
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- American Journal of Hematology, 2022, v. 97, n. 11, p. 1390, doi. 10.1002/ajh.26702
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- Article
Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features.
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- American Journal of Hematology, 2021, v. 96, n. 4, p. E117, doi. 10.1002/ajh.26096
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- Article
Haptoglobin genotype predicts severe acute vasoocclusive pain episodes in children with sickle cell anemia.
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- American Journal of Hematology, 2020, v. 95, n. 4, p. E92, doi. 10.1002/ajh.25728
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- Article
Treating sickle cell anemia: A new era dawns.
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- American Journal of Hematology, 2020, v. 95, n. 4, p. 338, doi. 10.1002/ajh.25724
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- Article
Airlie House legend.
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- American Journal of Hematology, 2018, v. 93, n. 12, p. 1566, doi. 10.1002/ajh.25293
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- Article
Fetal hemoglobin in sickle cell anemia: The Arab-Indian haplotype and new therapeutic agents.
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- American Journal of Hematology, 2017, v. 92, n. 11, p. 1233, doi. 10.1002/ajh.24872
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- Article
SIRT1 activates the expression of fetal hemoglobin genes.
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- American Journal of Hematology, 2017, v. 92, n. 11, p. 1177, doi. 10.1002/ajh.24879
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- Article
Genetic determinants of HbF in Saudi Arabian and African Benin haplotype sickle cell anemia.
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- American Journal of Hematology, 2017, v. 92, n. 9, p. E555, doi. 10.1002/ajh.24822
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- Article
Genetic modulation of fetal hemoglobin in hydroxyurea-treated sickle cell anemia.
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- American Journal of Hematology, 2017, v. 92, n. 5, p. E70, doi. 10.1002/ajh.24680
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- Article
Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.
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- American Journal of Hematology, 2016, v. 91, n. 6, p. E308, doi. 10.1002/ajh.24368
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- Article
The genetics of hemoglobin A<sub>2</sub> regulation in sickle cell anemia.
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- American Journal of Hematology, 2014, v. 89, n. 11, p. 1019, doi. 10.1002/ajh.23811
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- Article
A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia.
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- American Journal of Hematology, 2014, v. 89, n. 2, p. 187, doi. 10.1002/ajh.23613
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- Article
Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians.
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- American Journal of Hematology, 2013, v. 88, n. 11, p. E261, doi. 10.1002/ajh.23531
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- Article
Genetic modulation of HbF in Brazilians with HbSC disease and sickle cell anemia.
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- American Journal of Hematology, 2013, v. 88, n. 10, p. 923, doi. 10.1002/ajh.23538
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- Article
Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β<sup>0</sup> thalassemia.
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- American Journal of Hematology, 2013, v. 88, n. 6, p. 531, doi. 10.1002/ajh.23434
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- Article
Genetic modifiers of sickle cell disease.
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- American Journal of Hematology, 2012, v. 87, n. 8, p. 795, doi. 10.1002/ajh.23232
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- Article
A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype.
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- American Journal of Hematology, 2012, v. 87, n. 8, p. 824, doi. 10.1002/ajh.23239
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- Article
Framing the research agenda for sickle cell trait: Building on the current understanding of clinical events and their potential implications.
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- American Journal of Hematology, 2012, v. 87, n. 3, p. 340, doi. 10.1002/ajh.22271
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- Article
Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.
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- American Journal of Hematology, 2012, v. 87, n. 2, p. 217, doi. 10.1002/ajh.22221
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- Article
Is HbA<sub>2</sub> level a reliable diagnostic measurement for β-thalassemia trait in people with iron deficiency?
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- American Journal of Hematology, 2012, v. 87, n. 1, p. 114, doi. 10.1002/ajh.22188
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- Article
Erratum to: Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: A systematic review.
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- American Journal of Hematology, 2011, v. 86, n. 8, p. 722, doi. 10.1002/ajh.22074
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- Article
Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans.
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- American Journal of Hematology, 2011, v. 86, n. 7, p. 612, doi. 10.1002/ajh.22032
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- Article
G6PD deficiency and stroke in the CSSCD.
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- American Journal of Hematology, 2011, v. 86, n. 3, p. 331, doi. 10.1002/ajh.21958
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- Article
Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1.
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- American Journal of Hematology, 2011, v. 86, n. 2, p. 220, doi. 10.1002/ajh.21928
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- Article
Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: A systematic review.
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- American Journal of Hematology, 2010, v. 85, n. 11, p. 882, doi. 10.1002/ajh.21810
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- Article
Leg ulcers in sickle cell disease.
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- American Journal of Hematology, 2010, v. 85, n. 10, p. 831, doi. 10.1002/ajh.21838
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- Article
The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.
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- American Journal of Hematology, 2010, v. 85, n. 6, p. 403, doi. 10.1002/ajh.21699
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- Article
Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study.
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- American Journal of Hematology, 2010, v. 85, n. 1, p. 29, doi. 10.1002/ajh.21572
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- Article
Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions.
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- American Journal of Hematology, 2009, v. 84, n. 9, p. 618, doi. 10.1002/ajh.21475
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- Article
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
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- American Journal of Hematology, 2009, v. 84, n. 9, p. 603, doi. 10.1002/ajh.21480
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- Article
Genome-wide association studies and the genetic dissection of complex traits.
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- American Journal of Hematology, 2009, v. 84, n. 8, p. 504, doi. 10.1002/ajh.21440
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- Article
Hemoglobin Kenya composed of α- and (<sup>A</sup>γβ)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.
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- American Journal of Hematology, 2009, v. 84, n. 1, p. 55, doi. 10.1002/ajh.21308
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- Article
Pulmonary arterial hypertension and left-sided heart disease in sickle cell disease: Clinical characteristics and association with soluble adhesion molecule expression.
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- American Journal of Hematology, 2008, v. 83, n. 7, p. 547, doi. 10.1002/ajh.21187
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- Article
Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong Kong.
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- American Journal of Hematology, 2008, v. 83, n. 6, p. 458, doi. 10.1002/ajh.21150
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- Article
Sickle cell bone disease: Response to vitamin D and calcium.
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- American Journal of Hematology, 2008, v. 83, n. 4, p. 271, doi. 10.1002/ajh.21085
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- Article
Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations.
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- American Journal of Hematology, 2008, v. 83, n. 3, p. 189, doi. 10.1002/ajh.21048
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- Article
Clinical trials in sickle cell disease: Adopting the combination chemotherapy paradigm.
- Published in:
- American Journal of Hematology, 2008, v. 83, n. 1, p. 1, doi. 10.1002/ajh.21033
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- Article
Hemoglobin SE disease-A concise review.
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- American Journal of Hematology, 2007, v. 82, n. 7, p. 643, doi. 10.1002/ajh.20847
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- Article
Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B.
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- American Journal of Hematology, 2007, v. 82, n. 3, p. 179, doi. 10.1002/ajh.20800
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- Article
Lacrimal gland enlargement in sickle cell disease.
- Published in:
- American Journal of Hematology, 2006, v. 81, n. 11, p. 888, doi. 10.1002/ajh.20658
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- Article
Hemoglobinopathies mimicking Hb S/β‐thalassemia: Hb S/S with α‐thalassemia and Hb S/Volga.
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- American Journal of Hematology, 2006, v. 81, n. 5, p. 361, doi. 10.1002/ajh.20562
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- Article
Sickle cell vaso-occlusive crisis induces the release of circulating serum heat shock protein-70.
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- American Journal of Hematology, 2005, v. 78, n. 3, p. 240, doi. 10.1002/ajh.20292
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- Article
Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background.
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- American Journal of Hematology, 2004, v. 77, n. 4, p. 384, doi. 10.1002/ajh.20209
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- Article
N-Terminal Pro-Brain Natriuretic Peptide Levels and Risk of Death in Sickle Cell Disease.
- Published in:
- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 3, p. 310, doi. 10.1001/jama.296.3.310
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- Article
Long-term Use of Hydroxyurea for Sickle Cell Anemia—Reply.
- Published in:
- 2003
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- Publication type:
- Letter
Effect of Hydroxyurea on Mortality and Morbidity in Adult Sickle Cell Anemia: Risks and Benefits Up to 9 Years of Treatment.
- Published in:
- JAMA: Journal of the American Medical Association, 2003, v. 289, n. 13, p. 1645, doi. 10.1001/jama.289.13.1645
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- Article
Genomic approaches to identifying targets for treating β hemoglobinopathies.
- Published in:
- BMC Medical Genomics, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s12920-015-0120-2
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- Article