Maria F. Sonati

Campinas, SP, Brazil

Last Updated: 09/26/2026

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Found 12 publications

A novel α0-thalassemia deletion in a Brazilian child with Hb H disease: --Mococa.

A novel α0-thalassemia deletion in a Brazilian child with Hb H disease: --Mococa.

Journal: International journal of laboratory hematology

Published: January 04, 2024

Functional characterization of compound heterozygosity Hb S/Hb Deer Lodge in Brazil.

Functional characterization of compound heterozygosity Hb S/Hb Deer Lodge in Brazil.

Journal: Hematology, transfusion and cell therapy

Published: September 06, 2022

Endothelial Nitric Oxide Synthase (eNOS) Gene Polymorphisms and Markers of Hemolysis, Inflammation and Endothelial Dysfunction in Brazilian Sickle Cell Anemia Patients.

Endothelial Nitric Oxide Synthase (eNOS) Gene Polymorphisms and Markers of Hemolysis, Inflammation and Endothelial Dysfunction in Brazilian Sickle Cell Anemia Patients.

Journal: Biochemical genetics

Published: October 29, 2019

High levels of proinflammatory cytokines IL-6 and IL-8 are associated with a poor clinical outcome in sickle cell anemia.

High levels of proinflammatory cytokines IL-6 and IL-8 are associated with a poor clinical outcome in sickle cell anemia.

Journal: Annals of hematology

Published: October 01, 2019

Hemoglobin Kirklareli [Α2 59(E7) His>Leu; HBA2:c.176A>T] in a Brazilian child with severe dyspnea and low O2 saturation.

Hemoglobin Kirklareli [Α2 59(E7) His>Leu; HBA2:c.176A>T] in a Brazilian child with severe dyspnea and low O2 saturation.

Journal: Annals of hematology

Published: September 24, 2019

First report of εγδβ0 -thalassemia in a Brazilian family.

First report of εγδβ0 -thalassemia in a Brazilian family.

Journal: International journal of laboratory hematology

Published: June 01, 2018

Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child.

Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child.

Journal: Pediatric blood & cancer

Published: January 03, 2018

Understanding the molecular basis of the high oxygen affinity variant human hemoglobin Coimbra.

Understanding the molecular basis of the high oxygen affinity variant human hemoglobin Coimbra.

Journal: Archives of biochemistry and biophysics

Published: July 05, 2017

Coinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia.

Coinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia.

Journal: Hemoglobin

Published: July 04, 2017

A novel α0 -thalassemia deletion in a Brazilian child with Hb H disease [--(Braz) ].

A novel α0 -thalassemia deletion in a Brazilian child with Hb H disease [--(Braz) ].

Journal: International journal of laboratory hematology

Published: March 21, 2017

Expression profiles of phosphatidylinositol phosphate kinase genes during normal human in vitro erythropoiesis.

Expression profiles of phosphatidylinositol phosphate kinase genes during normal human in vitro erythropoiesis.

Journal: Genetics and molecular research : GMR

Published: December 06, 2012

A new β⁰-thalassemia frameshift mutation [β 48 (-T)] in a Uruguayan family.

A new β⁰-thalassemia frameshift mutation [β 48 (-T)] in a Uruguayan family.

Journal: International journal of laboratory hematology

Published: May 30, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026