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The impact of neonatal 17-hydroxyprogesterone cutoff determination in a public newborn screening program for congenital adrenal hyperplasia in Southern Brazil: 3 years’ experience

Endocrine Connections, 2023-12, Vol.12 (12), p.1-9

2023

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Epidemiological profile of congenital hypothyroidism at a southern Brazilian state

Archives of Endocrinology and Metabolism, 2023-05, Vol.67 (4), p.e000606

2023

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Twenty Years of Neonatal Screening for Sickle Cell Disease in Brazil: The Challenges of a Continental Country with High Genetic Heterogeneity

Journal of inborn errors of metabolism and screening, 2021, Vol.9

2021

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Blood Antioxidant Parameters in Sickle Cell Anemia Patients in Steady State

Journal of the National Medical Association, 2008-08, Vol.100 (8), p.897-902

2008

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Evaluation of the Genetic Screening Processor for the Performance of Newborn Screening Tests

Journal of inborn errors of metabolism and screening, 2016, Vol.4, p.232640981666937

2016

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Glucose-6-phosphate-dehydrogenase deficiency and its correlation with other risk factors in jaundiced newborns in Southern Brazil

Asian Pacific journal of tropical biomedicine, 2011-04, Vol.1 (2), p.110-113

2011

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An evaluation of IRT neonatal analytical performance in AutoDELFIA

Jornal brasileiro de patologia e medicina laboratorial, 2013-12, Vol.49 (6), p.388-390

2013

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A Low-Cost and Simple Genetic Screening for Cystic Fibrosis Provided by the Brazilian Public Health System

The Journal of pediatrics, 2018-08, Vol.199, p.272-277.e3

2018

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Neonatal screening for congenital adrenal hyperplasia in Southern Brazil: a population based study with 108,409 infants

BMC pediatrics, 2017-01, Vol.17 (1), p.22-22, Article 22

2017

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Evaluation of RET-He values as an early indicator of iron deficiency anemia in pregnant women

Hematology, Transfusion and Cell Therapy, 2023-01, Vol.45 (1), p.52-57

2023

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Flow Cytometry in Detection of Fetal Red Blood Cells and Maternal F Cells to Identify Fetomaternal Hemorrhage

Fetal and pediatric pathology, 2016-11, Vol.35 (6), p.385-391

2016

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UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?

Pediatric research, 2012-08, Vol.72 (2), p.169-173

2012

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Neutrophil CD64 expression as an important diagnostic marker of infection and sepsis in hospital patients

Journal of immunological methods, 2014-12, Vol.414, p.65-68

2014

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O Papel do Farmacêutico nos Primeiros Socorros em Intoxicações

de Castro, Simone Martins

2020

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SAT-098 The Impact of 17-OHP Cutoffs Determination in a Public Newborn Screening Program for Congenital Adrenal Hyperplasia in Southern Brazil: A Three Years’ Experience

Journal of the Endocrine Society, 2020-05, Vol.4 (Supplement_1)

2020

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Reticulocytes indices in β thalassemia trait individuals

Revista brasileira de hematologia e hemoterapia, 2011-01, Vol.33 (5), p.396-397

2011

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Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia

Molecular diagnosis & therapy, 2017-12, Vol.21 (6), p.663-675

2017

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Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?

Molecular diagnosis & therapy, 2017-08, Vol.21 (4), p.437-442

2017

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Definition of reference ranges for the platelet distribution width (PDW): a local need

Clinical chemistry and laboratory medicine, 2010-02, Vol.48 (2), p.255-257

2010

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Avaliação dos indicadores de um serviço de referência em triagem neonatal no sul do Brasil durante a pandemia por COVID-19

Saúde Coletiva (Barueri), 2022-01, Vol.12 (2), p.9610-9625

2022

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Characterization of Patients with Chronic Myeloid Leukemia Unresponsive to Tyrosine Kinase Inhibitors Who Underwent Allogeneic Hematopoietic Stem Cell Transplantation

International journal of hematology- oncology and stem cell research, 2017-01, Vol.11 (1), p.30-36

2017

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Diagnóstico laboratorial das leucemias linfóides agudas

Jornal brasileiro de patologia e medicina laboratorial, 2004-04, Vol.40 (2), p.91-98

2004

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Low prevalence of primary antiretroviral resistance mutations and predominance of HIV-1 clade C at polymerase gene in newly diagnosed individuals from south Brazil

Virus research, 2006-03, Vol.116 (1), p.201-207

2006

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Polymorphic Variants of UGT1A1 in Neonatal Jaundice in Southern Brazil

Journal of tropical pediatrics (1980), 2010-10, Vol.56 (5), p.366-367

2010

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Prevalence of UGT1A1 gene polymorphism in patients with hemolytic anemia in southern Brazil

Genetic testing and molecular biomarkers, 2011-01, Vol.15 (1-2), p.107-110

2011

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The impact of neonatal 17-hydroxyprogesterone cutoff determination in a public newborn screening program for congenital adrenal hyperplasia in Southern Brazil: 3 years’ experience

Epidemiological profile of congenital hypothyroidism at a southern Brazilian state

Twenty Years of Neonatal Screening for Sickle Cell Disease in Brazil: The Challenges of a Continental Country with High Genetic Heterogeneity

Blood Antioxidant Parameters in Sickle Cell Anemia Patients in Steady State

Evaluation of the Genetic Screening Processor for the Performance of Newborn Screening Tests

Glucose-6-phosphate-dehydrogenase deficiency and its correlation with other risk factors in jaundiced newborns in Southern Brazil

An evaluation of IRT neonatal analytical performance in AutoDELFIA

A Low-Cost and Simple Genetic Screening for Cystic Fibrosis Provided by the Brazilian Public Health System

Neonatal screening for congenital adrenal hyperplasia in Southern Brazil: a population based study with 108,409 infants

Evaluation of RET-He values as an early indicator of iron deficiency anemia in pregnant women

Flow Cytometry in Detection of Fetal Red Blood Cells and Maternal F Cells to Identify Fetomaternal Hemorrhage

UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?

Neutrophil CD64 expression as an important diagnostic marker of infection and sepsis in hospital patients

O Papel do Farmacêutico nos Primeiros Socorros em Intoxicações

SAT-098 The Impact of 17-OHP Cutoffs Determination in a Public Newborn Screening Program for Congenital Adrenal Hyperplasia in Southern Brazil: A Three Years’ Experience

Reticulocytes indices in β thalassemia trait individuals

Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia

Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?

Definition of reference ranges for the platelet distribution width (PDW): a local need

Avaliação dos indicadores de um serviço de referência em triagem neonatal no sul do Brasil durante a pandemia por COVID-19

Characterization of Patients with Chronic Myeloid Leukemia Unresponsive to Tyrosine Kinase Inhibitors Who Underwent Allogeneic Hematopoietic Stem Cell Transplantation

Diagnóstico laboratorial das leucemias linfóides agudas

Low prevalence of primary antiretroviral resistance mutations and predominance of HIV-1 clade C at polymerase gene in newly diagnosed individuals from south Brazil

Polymorphic Variants of UGT1A1 in Neonatal Jaundice in Southern Brazil

Prevalence of UGT1A1 gene polymorphism in patients with hemolytic anemia in southern Brazil

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