Rahyssa R. Sales

Belo Horizonte, MG 31270901, Brazil

Last Updated: 09/26/2026

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Found 11 publications

Effect of haplotypes of functional SNPs related to expression of fetal hemoglobin (HbF) on clinical prognosis of hematological malignancies.

Effect of haplotypes of functional SNPs related to expression of fetal hemoglobin (HbF) on clinical prognosis of hematological malignancies.

Journal: International journal of hematology

Published: January 23, 2023

Pharmacogenomics of hydroxyurea therapy and fetal hemoglobin levels in sickle cell anemia.

Pharmacogenomics of hydroxyurea therapy and fetal hemoglobin levels in sickle cell anemia.

Journal: Pharmacogenomics

Published: May 13, 2022

Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia.

Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia.

Journal: Journal of human genetics

Published: April 06, 2022

Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis.

Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis.

Journal: Frontiers in pharmacology

Published: September 18, 2021

Prevalence and risk factors for albuminuria and glomerular hyperfiltration in a large cohort of children with sickle cell anemia.

Prevalence and risk factors for albuminuria and glomerular hyperfiltration in a large cohort of children with sickle cell anemia.

Journal: American journal of hematology

Published: February 03, 2020

Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia.

Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia.

Journal: Annals of hematology

Published: December 11, 2019

Interleukin-10 haplotypes are not associated with acute cerebral ischemia or high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.

Interleukin-10 haplotypes are not associated with acute cerebral ischemia or high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.

Journal: Revista brasileira de hematologia e hemoterapia

Published: July 14, 2016

The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.

The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.

Journal: Hemoglobin

Published: April 28, 2016

Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.

Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.

Journal: Annals of hematology

Published: February 29, 2016

Association between ENPP1 K173Q and stroke in a newborn cohort of 395 Brazilian children with sickle cell anemia.

Association between ENPP1 K173Q and stroke in a newborn cohort of 395 Brazilian children with sickle cell anemia.

Journal: Blood

Published: September 05, 2015

Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children.

Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children.

Journal: Revista brasileira de hematologia e hemoterapia

Published: November 17, 2014

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Last Updated: 09/26/2026