Edis Belini-Junior

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 .

Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia

M. Bezerra, I. F. Domingos, A. Araújo, 2020, Hematology, transfusion and cell therapy.

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.

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.

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.

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.