R. G. Oliveira

Relationship between adenosine deaminase polymorphism (c.22G > A) and oxidative stress in sickle cell anemia

Jéssika V Okumura, Danilo G H Silva, L. Torres, 2017 .

Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein

K. Mimura, S. Oliani, Jéssika V Okumura, 2016, PloS one.

Inheritance of the Bantu/Benin haplotype causes less severe hemolytic and oxidative stress in sickle cell anemia patients treated with hydroxycarbamide

G. B. Gelaleti, Jéssika V Okumura, Danilo G H Silva, 2016, Journal of Human Genetics.

Correction: Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein

S. Oliani, Jéssika V Okumura, L. Torres, 2017, PloS one.

Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab

S. Oliani, Jéssika V Okumura, L. Torres, 2016, Hemoglobin.

Hemoglobin (Hb) Val de Marne (Hb Footscray) in Brazil: the first case report.

E. Belini-Junior, C. Bonini-Domingos, R. G. Oliveira, 2016, Genetics and molecular research : GMR.

Plasma levels of TGF-b 1 in homeostasis of the inflammation in sickle cell disease

C. Lobo, R. G. Oliveira, Danilo Grünig, 2016 .