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Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation

Pediatric diabetes, 2010-11, Vol.11 (7), p.505-508

2010

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Brazilian Residents' Attitude and Practice Toward Sexual Health Issues in Pregnant Patients

Journal of sexual medicine, 2012-10, Vol.9 (10), p.2516-2524

2012

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Living Conditions as a Driving Factor in Persistent Methicillin-resistant Staphylococcus aureus Colonization Among HIV-infected Youth

The Pediatric infectious disease journal, 2016-10, Vol.35 (10), p.1126-1131

2016

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Hereditary corticosteroid-binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred

Clinical endocrinology (Oxford), 2003-06, Vol.58 (6), p.756-762

2003

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Children with Cushing's syndrome: primary pigmented nodular adrenocortical disease should always be suspected

Pituitary, 2011-03, Vol.14 (1), p.61-67

2011

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Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Cav1·1) are not associated with thyrotoxic hypokalaemic periodic paralysis

Clinical endocrinology (Oxford), 2002-03, Vol.56 (3), p.367-375

2002

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Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay

The journal of clinical endocrinology and metabolism, 2003-01, Vol.88 (1), p.38-44

2003

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Central precocious puberty associated with pituitary duplication and midline defects

Journal of Pediatric Endocrinology and Metabolism, 2007-10, Vol.20 (10), p.1141

2007

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The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency

Endocrine, 2006-12, Vol.30 (3), p.365-369

2006

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Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency

Arquivos brasileiros de endocrinologia e metabologia, 2007-10, Vol.51 (7), p.1097-1103

2007

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Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel alpha1 subunit gene (Cav1.1) are not associated with thyrotoxic hypokalaemic periodic paralysis

Clinical endocrinology (Oxford), 2002-03, Vol.56 (3), p.367-375

2002

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Adenomas hipofisários produtores de glicoproteínas: patogênese, diagnóstico e tratamento

Arquivos brasileiros de endocrinologia e metabologia, 2005-10, Vol.49 (5), p.657-673

2005

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Glycoprotein-secreting pituitary adenomas: pathogenesis, diagnosis and treatment

Arquivos brasileiros de endocrinologia e metabologia, 2005-10, Vol.49 (5), p.657-673

2005

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Adenomas hipofisários produtores de glicoproteínas: patogênese, diagnóstico e tratamento

Arquivos brasileiros de endocrinologia e metabologia, 2005-10, Vol.49 (5), p.657-673

2005

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Terapia de reposição hormonal no hipopituitarismo

Arquivos brasileiros de endocrinologia e metabologia, 2003-08, Vol.47 (4), p.492-508

2003

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Terapia de reposição hormonal no hipopituitarismo

Arquivos brasileiros de endocrinologia e metabologia, 2003-08, Vol.47 (4), p.492-508

2003

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ANIPHI: An innovative pedagogical platform based on the Delphi method to support animal welfare teaching

PloS one, 2022-11, Vol.17 (11), p.e0277189-e0277189

2022

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Dairy products, calcium, and prostate cancer risk: a systematic review and meta-analysis of cohort studies

The American journal of clinical nutrition, 2015, Vol.101 (1), p.87-117

2015

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Red and processed meat intake and risk of colorectal adenomas: a systematic review and meta-analysis of epidemiological studies

Cancer causes & control, 2013-04, Vol.24 (4), p.611-627

2013

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Red and processed meat and colorectal cancer incidence: meta-analysis of prospective studies

PloS one, 2011-06, Vol.6 (6), p.e20456

2011

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Diagnosis of Human Leptospirosis in a Clinical Setting: Real-Time PCR High Resolution Melting Analysis for Detection of Leptospira at the Onset of Disease

Scientific reports, 2018-06, Vol.8 (1), p.9213-10, Article 9213

2018

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Vaccination status and long COVID symptoms in patients discharged from hospital

Scientific reports, 2023-02, Vol.13 (1), p.2481-2481, Article 2481

2023

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Effect of soft tissue noise on trabecular bone score in postmenopausal women with diabetes: A cross sectional study

Bone (New York, N.Y.), 2022-04, Vol.157, p.116339-116339, Article 116339

2022

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Fusion Oncogenes Are the Main Genetic Events Found in Sporadic Papillary Thyroid Carcinomas from Children

Thyroid (New York, N.Y.), 2017-02, Vol.27 (2), p.182-188

2017

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Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation

Brazilian Residents' Attitude and Practice Toward Sexual Health Issues in Pregnant Patients

Living Conditions as a Driving Factor in Persistent Methicillin-resistant Staphylococcus aureus Colonization Among HIV-infected Youth

Hereditary corticosteroid-binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred

Children with Cushing's syndrome: primary pigmented nodular adrenocortical disease should always be suspected

Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Cav1·1) are not associated with thyrotoxic hypokalaemic periodic paralysis

Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay

Central precocious puberty associated with pituitary duplication and midline defects

The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency

Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency

Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel alpha1 subunit gene (Cav1.1) are not associated with thyrotoxic hypokalaemic periodic paralysis

Adenomas hipofisários produtores de glicoproteínas: patogênese, diagnóstico e tratamento

Glycoprotein-secreting pituitary adenomas: pathogenesis, diagnosis and treatment

Adenomas hipofisários produtores de glicoproteínas: patogênese, diagnóstico e tratamento

Terapia de reposição hormonal no hipopituitarismo

Terapia de reposição hormonal no hipopituitarismo

ANIPHI: An innovative pedagogical platform based on the Delphi method to support animal welfare teaching

Dairy products, calcium, and prostate cancer risk: a systematic review and meta-analysis of cohort studies

Red and processed meat intake and risk of colorectal adenomas: a systematic review and meta-analysis of epidemiological studies

“Chagas Express XXI”: A new ArtScience social technology for health and science education—A case study in Brazilian endemic areas of Chagas disease with an active search of chronic cases

Red and processed meat and colorectal cancer incidence: meta-analysis of prospective studies

Diagnosis of Human Leptospirosis in a Clinical Setting: Real-Time PCR High Resolution Melting Analysis for Detection of Leptospira at the Onset of Disease

Vaccination status and long COVID symptoms in patients discharged from hospital

Effect of soft tissue noise on trabecular bone score in postmenopausal women with diabetes: A cross sectional study

Fusion Oncogenes Are the Main Genetic Events Found in Sporadic Papillary Thyroid Carcinomas from Children

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