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Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia

Genetics and molecular biology, 2021-01, Vol.44 (2), p.e20200399-e20200399

2021

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Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients

Annals of hematology, 2021-11, Vol.100 (11), p.2669-2676

2021

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Hemograms and serial hemogram-derived ratios in survivors and non-survivors of COVID-19 in Campinas, Brazil

Hematology, Transfusion and Cell Therapy, 2024-01, Vol.46 (1), p.14-21

2024

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Serum folate and cytokines in heterozygous β‐thalassemia

International journal of laboratory hematology, 2020-12, Vol.42 (6), p.718-726

2020

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Prevalence of α-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, Brazil

Genetics and molecular biology, 2012-01, Vol.35 (3), p.594-598

2012

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Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients

Hematology, Transfusion and Cell Therapy, 2021-04, Vol.43 (2), p.165-170

2021

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Differential profile of PIP4K2A expression in hematological malignancies

Blood cells, molecules, & diseases, 2015-10, Vol.55 (3), p.228-235

2015

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

Genetics and molecular biology, 2011-01, Vol.34 (3), p.425-428

2011

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

Genetics and molecular biology, 2011-01, Vol.34 (3), p.421-424

2011

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Beyond the Definitions of the Phenotypic Complications of Sickle Cell Disease : An Update on Management

TheScientificWorld, 2012-01, Vol.2012 (2012), p.1-55

2012

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Polymorphism of human haptoglobin and its clinical importance

Genetics and molecular biology, 2008, Vol.31 (3), p.602-620

2008

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PIP4KIIα Gene Silencing by Lentivirus-Mediated Delivery of shRNA in Human K562 Cells

Blood, 2011-11, Vol.118 (21), p.3200-3200

2011

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The genetics of blood disorders: hereditary hemoglobinopathies

Jornal de pediatria, 2008-08, Vol.84 (4 Suppl), p.S40-S51

2008

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The CCR5Δ32 Polymorphism in Brazilian Patients with Sickle Cell Disease

Disease markers, 2014-01, Vol.2014 (2014), p.1-4

2014

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Evidences of the PI5P Increasing the Expression of HBG and Gamma Globin Concentrations

Blood, 2021-11, Vol.138 (Supplement 1), p.947-947

2021

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Interleukin 8 Level, Reticulocyte Counting and aPTT Ratio in Brazilian Sickle Cell Anemia Patients with Leg Ulcers

Blood, 2011-11, Vol.118 (21), p.4835-4835

2011

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Sphingomyelin and Phosphatidylserine Derived Compounds Found into RBCs of Two Unrelated Individuals with Idiopathic Erythrocytosis with Altered Hemoglobin (Hb) Function Properties and No Hemoglobinopathies - Preliminary Results

Blood, 2022-11, Vol.140 (Supplement 1), p.11052-11053

2022

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Expression Profile of PIP Kinases During In Vitro Human Erythropoiesis

Blood, 2010-11, Vol.116 (21), p.2079-2079

2010

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Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population

Genetics and molecular biology, 2013-01, Vol.36 (3), p.316-322

2013

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Three New α-Globin Variants: Hb Itapira [α30(B11)Glu→Val (α1)], Hb Bom Jesus Da Lapa [α30(B11)Glu→Ala (α1)] and Hb Boa Esperança [α16(A14)Lys→Thr (α2)]

Hemoglobin, 2007-01, Vol.31 (2), p.151-157

2007

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Functional Properties of Hb S and Hb C in Stored Cpda-1 Red Blood Cells Concentrate — a Prospective Study

Blood, 2018-11, Vol.132 (Supplement 1), p.2548-2548

2018

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Genética das doenças hematológicas: as hemoglobinopatias hereditárias

Jornal de pediatria, 2008-08, Vol.84 (4 suppl), p.S40-S51

2008

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Lymphocyte Ratios Progressively Worsen in Non-Survivors of COVID-19

Blood, 2021-11, Vol.138 (Supplement 1), p.4196-4196

2021

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Identificação e caracterização de variantes novas e raras da hemoglobina humana

Revista brasileira de hematologia e hemoterapia, 2008-08, Vol.30 (4), p.316-319

2008

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Haptoglobin polymorphism and diabetic nephropathy in Brazilian diabetic patients

Annals of human biology, 2009-01, Vol.36 (4), p.437-441

2009

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Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia

Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients

Hemograms and serial hemogram-derived ratios in survivors and non-survivors of COVID-19 in Campinas, Brazil

Serum folate and cytokines in heterozygous β‐thalassemia

Prevalence of α-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, Brazil

Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients

Differential profile of PIP4K2A expression in hematological malignancies

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

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

Beyond the Definitions of the Phenotypic Complications of Sickle Cell Disease : An Update on Management

Polymorphism of human haptoglobin and its clinical importance

PIP4KIIα Gene Silencing by Lentivirus-Mediated Delivery of shRNA in Human K562 Cells

The genetics of blood disorders: hereditary hemoglobinopathies

The CCR5Δ32 Polymorphism in Brazilian Patients with Sickle Cell Disease

Evidences of the PI5P Increasing the Expression of HBG and Gamma Globin Concentrations

Interleukin 8 Level, Reticulocyte Counting and aPTT Ratio in Brazilian Sickle Cell Anemia Patients with Leg Ulcers

Sphingomyelin and Phosphatidylserine Derived Compounds Found into RBCs of Two Unrelated Individuals with Idiopathic Erythrocytosis with Altered Hemoglobin (Hb) Function Properties and No Hemoglobinopathies - Preliminary Results

Expression Profile of PIP Kinases During In Vitro Human Erythropoiesis

Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population

Three New α-Globin Variants: Hb Itapira [α30(B11)Glu→Val (α1)], Hb Bom Jesus Da Lapa [α30(B11)Glu→Ala (α1)] and Hb Boa Esperança [α16(A14)Lys→Thr (α2)]

Functional Properties of Hb S and Hb C in Stored Cpda-1 Red Blood Cells Concentrate — a Prospective Study

Genética das doenças hematológicas: as hemoglobinopatias hereditárias

Lymphocyte Ratios Progressively Worsen in Non-Survivors of COVID-19

Identificação e caracterização de variantes novas e raras da hemoglobina humana

Haptoglobin polymorphism and diabetic nephropathy in Brazilian diabetic patients

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