List of works - Fernando Ferreira Costa

Band 3 Campinas: a novel splicing mutation in the band 3 gene (AE1) associated with hereditary spherocytosis, hyperactivity of Na+/Li+ countertransport and an abnormal renal bicarbonate handling ⬇️

scientific article published on October 1, 1997

Characterization of alpha thalassemic genotypes by multiplex ligation-dependent probe amplification in the Brazilian population ⬇️

scientific article published on December 17, 2010

Characterization of beta-thalassemia mutations in patients from the state of Rio Grande do Norte, Brazil ⬇️

scientific article published on July 1, 2011

Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosis ⬇️

scientific article published on 01 September 1996

Demographic history differences between Hispanics and Brazilians imprint haplotype features

scientific article published in 2022

Design, Synthesis, and Pharmacological Evaluation of Novel Hybrid Compounds To Treat Sickle Cell Disease Symptoms ⬇️

scientific article published on July 25, 2011

Determination of βS haplotypes in patients with sickle-cell anemia in the state of Rio Grande do Norte, Brazil ⬇️

scientific article published on July 1, 2011

Downregulation of IRS2 in myelodysplastic syndrome: A possible role in impaired hematopoietic cell differentiation ⬇️

scientific article published on March 31, 2012

Early circulating erythroid progenitor cells and expression of erythropoietin receptors in sickle cell disease ⬇️

scientific article published on 01 April 1998

Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients ⬇️

scientific article published on October 15, 1995

Factor V Leiden (FVQ 506) is common in a Brazilian population ⬇️

scientific article published on July 1, 1995

Genetic Analysis of β-Thalassemia Major and β-Thalassemia Intermedia in Brazil ⬇️

scientific article published on May 1, 1998

Haptoglobin Gene Polymorphism in Patients with Sickle Cell Anemia: Findings from a Nigerian Cohort Study

scientific article published on 08 May 2020

Haptoglobin Genotypes in Sickle-Cell Disease ⬇️

scientific article published on 08 June 2011

Mechanical properties of stored red blood cells using optical tweezers ⬇️

scientific article published on October 15, 1998

Mild hemolysis in a girl with G6PD Sumaré (class I variant) associated with G6PD A− ⬇️

scientific article published on May 1, 2003

Minimal doses of hydroxyurea for sickle cell disease ⬇️

scientific article published on 01 August 1997

Molecular characteristics and chromatin texture features in acute promyelocytic leukemia ⬇️

scientific article published on June 28, 2012

Prevalence of homozygosity for the deleted alleles of glutathione S‐transferase mu (GSTMl) and theta (GSTTl) among distinct ethnic groutx from Brazil: relevance to enviromental carcinogenesis? ⬇️

scientific article published on 01 September 1998

Prevalence of the mutation C677 ? T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil ⬇️

scientific article published on July 24, 1998

Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease

scientific article published on 01 December 1997

Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil