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1.
Polymorphisms and gene expression of metalloproteinases and their inhibitors associated with cerebral ischemic stroke in young patients with sickle cell anemia.
Mol Biol Rep
; 50(4): 3341-3353, 2023 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-36720795
2.
Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients.
Ann Hematol
; 100(11): 2669-2676, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-34453189
3.
Alpha thalassemia, but not ßS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort.
Ann Hematol
; 100(4): 921-931, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33586016
4.
CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome.
Genet Mol Biol
; 41(4): 727-734, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30508004
5.
Combined genotypes of the MBL2 gene related to low mannose-binding lectin levels are associated with vaso-occlusive events in children with sickle cell anemia.
Genet Mol Biol
; 40(3): 600-603, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28837214
6.
Evaluation of CD4(+)CD25(+)FoxP3(+) T cell populations, IL-10 production, and their correlation with clinical and biochemical parameters in sickle cell anemia patients with leg ulcers.
Cytokine
; 75(2): 310-5, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26210477
7.
Erythropoiesis-driven regulation of hepcidin in human red cell disorders is better reflected through concentrations of soluble transferrin receptor rather than growth differentiation factor 15.
Am J Hematol
; 89(4): 385-90, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24860871
8.
Association between the genetic polymorphisms of glutathione S-transferase (GSTM1 and GSTT1) and the clinical manifestations in sickle cell anemia.
Blood Cells Mol Dis
; 51(2): 76-9, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23590899
9.
Comparison of DNA extraction methods for COVID-19 host genetics studies.
PLoS One
; 18(10): e0287551, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37903126
10.
Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients.
Hematol Transfus Cell Ther
; 43(2): 165-170, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-32461055
11.
Association of the SOD2 Polymorphism (Val16Ala) and SOD Activity with Vaso-occlusive Crisis and Acute Splenic Sequestration in Children with Sickle Cell Anemia.
Mediterr J Hematol Infect Dis
; 10(1): e2018012, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29531649
12.
The first reported case of factor V Leiden mutation with agenesis of superior vena cava: A case report.
Medicine (Baltimore)
; 97(22): e10511, 2018 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-29851773
13.
Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients
Hematol., Transfus. Cell Ther. (Impr.)
; 43(2): 165-170, Apr.-June 2021. tab
Artículo
en Inglés
| LILACS | ID: biblio-1286677
14.
Single Nucleotide Polymorphisms at +191 and +292 of Galectin-3 Gene (LGALS3) Related to Lower GAL-3 Serum Levels Are Associated with Frequent Respiratory Tract Infection and Vaso-Occlusive Crisis in Children with Sickle Cell Anemia.
PLoS One
; 11(9): e0162297, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27603703
15.
The CCR5Δ32 polymorphism in Brazilian patients with sickle cell disease.
Dis Markers
; 2014: 678246, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-25548430
16.
Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients.
Exp Biol Med (Maywood)
; 244(11): 932-939, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31079484
17.
Interaction between hemoglobin S and N-Baltimore: a case report in Pernambuco, Brazil.
Hematol Transfus Cell Ther
; 41(4): 365-368, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31126755
18.
JAK2 V617F mutation prevalence in myeloproliferative neoplasms in Pernambuco, Brazil.
Genet Test Mol Biomarkers
; 16(7): 802-5, 2012 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-22304488
19.
Combined genotypes of the MBL2 gene related to low mannose-binding lectin levels are associated with vaso-occlusive events in children with sickle cell anemia
Genet. mol. biol
; 40(3): 600-603, July-Sept. 2017. tab, graf
Artículo
en Inglés
| LILACS | ID: biblio-892435
20.
Haptoglobin genotypes in sickle-cell disease.
Genet Test Mol Biomarkers
; 15(10): 709-13, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21651321