Found: 18
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Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-34396-1
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- Article
Leg Ulcers in Sickle Cell Disease: A Multifactorial Analysis Highlights the Hemolytic Profile.
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- Hematology Reports, 2023, v. 15, n. 1, p. 119, doi. 10.3390/hematolrep15010013
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- Article
Evaluation of Alpha-1 Antitrypsin Levels and SERPINA1 Gene Polymorphisms in Sickle Cell Disease.
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- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01491
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- Article
A Description of the Hemolytic Component in Sickle Leg Ulcer: The Role of Circulating miR-199a-5p, miR-144, and miR-126.
- Published in:
- Biomolecules (2218-273X), 2022, v. 12, n. 2, p. 317, doi. 10.3390/biom12020317
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- Article
Sickle Cell Anemia: Variants in the CYP2D6 , CAT , and SLC14A1 Genes Are Associated With Improved Hydroxyurea Response.
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- Frontiers in Pharmacology, 2020, v. 11, p. N.PAG, doi. 10.3389/fphar.2020.553064
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- Article
Priapism in sickle cell disease: Associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers.
- Published in:
- PLoS ONE, 2021, v. 16, n. 2, p. 1, doi. 10.1371/journal.pone.0246067
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- Article
Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC).
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- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0228399
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- Article
Genetic Polymorphisms Associated with Environmental Exposure to Polycyclic Derivatives in African Children.
- Published in:
- Disease Markers, 2018, p. 1, doi. 10.1155/2018/9078939
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- Publication type:
- Article
Sickle Cell Anemia Patients in Use of Hydroxyurea: Association between Polymorphisms in Genes Encoding Metabolizing Drug Enzymes and Laboratory Parameters.
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- Disease Markers, 2018, p. 1, doi. 10.1155/2018/6105691
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- Publication type:
- Article
Laboratory and Genetic Biomarkers Associated with Cerebral Blood Flow Velocity in Hemoglobin SC Disease.
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- Disease Markers, 2017, p. 1, doi. 10.1155/2017/6359871
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- Article
Transcranial Doppler in hemoglobin SC disease.
- Published in:
- 2017
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- Publication type:
- journal article
Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia.
- Published in:
- Lipids in Health & Disease, 2017, v. 16, p. 1, doi. 10.1186/s12944-017-0454-1
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- Article
Genetic modulation of fetal hemoglobin in hydroxyurea-treated sickle cell anemia.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 5, p. E70, doi. 10.1002/ajh.24680
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- Publication type:
- Article
TGFBR3 Polymorphisms (rs1805110 and rs7526590) Are Associated with Laboratory Biomarkers and Clinical Manifestations in Sickle Cell Anemia.
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- Disease Markers, 2020, p. 1, doi. 10.1155/2020/8867986
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- Article
Investigation of Lipid Profile and Clinical Manifestations in SCA Children.
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- Disease Markers, 2020, p. 1, doi. 10.1155/2020/8842362
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- Article
Effect of N(Epsilon)-(carboxymethyl)lysine on Laboratory Parameters and Its Association with β<sup>S</sup> Haplotype in Children with Sickle Cell Anemia.
- Published in:
- Disease Markers, 2019, p. 1, doi. 10.1155/2019/1580485
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- Publication type:
- Article
Evaluation of Cardiometabolic Parameters among Obese Women Using Oral Contraceptives.
- Published in:
- Frontiers in Endocrinology, 2017, p. 1, doi. 10.3389/fendo.2017.00256
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- Publication type:
- Article
Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia.
- Published in:
- PLoS ONE, 2019, v. 14, n. 7, p. 1, doi. 10.1371/journal.pone.0218040
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- Article