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Insulin Resistance in Congenital Adrenal Hyperplasia is Compensated for by Reduced Insulin Clearance

The journal of clinical endocrinology and metabolism, 2021-04, Vol.106 (4), p.e1574-e1585

2021

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Systematic review of quality of life in Turner syndrome

Quality of life research, 2018-08, Vol.27 (8), p.1985-2006

2018

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X‐linked congenital adrenal hypoplasia: Report of long clinical follow‐up and description of a new complex variant in the NR0B1 gene

American journal of medical genetics. Part A, 2024-06, Vol.194 (6), p.e63536-n/a

2024

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Anthropometry and physical appearance can be associated with quality of life in Brazilian women with Turner syndrome

Archives of Endocrinology and Metabolism, 2023-01, Vol.67 (1), p.126-135

2023

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Normal ambulatory blood pressure in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy

Archives of Endocrinology and Metabolism, 2023-01, Vol.67 (1), p.64

2023

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Functional and Structural Consequences of Nine CYP21A2 Mutations Ranging from Very Mild to Severe Effects

International Journal of Endocrinology, 2016-01, Vol.2016, p.4209670-10

2016

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ENERGY EXPENDITURE IN 21-HYDROXYLASE CONGENITAL ADRENAL HYPERPLASIA PATIENTS AND COMPARISON WITH PREDICTIVE EQUATIONS

Endocrine practice, 2020-04, Vol.26 (4), p.388-398

2020

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The bone densitometry is normal in Turner syndrome prepubertal patients after height age correction

Revista Brasileira de Saúde Materno Infantil, 2021-12, Vol.21 (4), p.1129-1134

2021

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FSH may be a useful tool to allow early diagnosis of Turner syndrome

BMC endocrine disorders, 2018-02, Vol.18 (1), p.8-8, Article 8

2018

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Normal bone health in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy

Osteoporosis international, 2022, Vol.33 (1), p.283-291

2022

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Fat Distribution and Lipid Profile of Young Adults with Congenital Adrenal Hyperplasia Due to 21‐Hydroxylase Enzyme Deficiency

Lipids, 2021-01, Vol.56 (1), p.101-110

2021

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Growth Curves for Girls with Turner Syndrome

BioMed research international, 2014-01, Vol.2014, p.687978-8

2014

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Cardiovascular dysfunction risk in young adults with congenital adrenal hyperplasia caused by 21‐hydroxylase enzyme deficiency

International journal of clinical practice (Esher), 2021-07, Vol.75 (7), p.e14233-n/a

2021

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Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia

Clinical biochemistry, 2019-11, Vol.73, p.50-56

2019

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Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density

Journal of bone and mineral metabolism, 2003-01, Vol.21 (6), p.396-401

2003

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A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins

Diabetology and metabolic syndrome, 2015-11, Vol.7 (96), p.101, Article 101

2015

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Turner syndrome and metabolic derangements: Another example of fetal programming

Early human development, 2012-02, Vol.88 (2), p.99-102

2012

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Crescimento e composição corporal de uma coorte de crianças e adolescentes com diabetes tipo 1

Arquivos brasileiros de endocrinologia e metabologia, 2013-11, Vol.57 (8), p.623-631

2013

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Growth hormone effect on body composition in Turner syndrome

Endocrine, 2011-12, Vol.40 (3), p.486-491

2011

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Impairment in Anthropometric Parameters and Body Composition in Females with Classical 21-Hydroxylase Deficiency

Journal of Pediatric Endocrinology and Metabolism, 2009-06, Vol.22 (6), p.519-530

2009

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Clinical and laboratory profile of pediatric and adolescent patients with type 1 diabetes

Jornal de pediatria, 2009-11, Vol.85 (6), p.490-494

2009

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Composição corporal em mulheres com deficiência da 21-hidroxilase: comparação dos métodos antropométricos e de impedância bioelétrica em relação a um grupo controle

Arquivos brasileiros de endocrinologia e metabologia, 2010-03, Vol.54 (3), p.274-281

2010

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A inclusão de novas técnicas de análise citogenética aperfeiçoou o diagnóstico cromossômico da síndrome de Turner

Arquivos brasileiros de endocrinologia e metabologia, 2009-12, Vol.53 (9), p.1137-1142

2009

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Bioelectrical Impedance Phase Angle and Its Determinants in Patients with Classic Congenital Adrenal Hyperplasia

Journal of the American College of Nutrition, 2022-05, Vol.ahead-of-print (ahead-of-print), p.1-8

2022

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Spontaneous final height in Turner's syndrome in Brazil

Journal of pediatric endocrinology & metabolism : JPEM, 2007-11, Vol.20 (11), p.1207

2007

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Insulin Resistance in Congenital Adrenal Hyperplasia is Compensated for by Reduced Insulin Clearance

Systematic review of quality of life in Turner syndrome

X‐linked congenital adrenal hypoplasia: Report of long clinical follow‐up and description of a new complex variant in the NR0B1 gene

Anthropometry and physical appearance can be associated with quality of life in Brazilian women with Turner syndrome

Normal ambulatory blood pressure in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy

Functional and Structural Consequences of Nine CYP21A2 Mutations Ranging from Very Mild to Severe Effects

ENERGY EXPENDITURE IN 21-HYDROXYLASE CONGENITAL ADRENAL HYPERPLASIA PATIENTS AND COMPARISON WITH PREDICTIVE EQUATIONS

The bone densitometry is normal in Turner syndrome prepubertal patients after height age correction

FSH may be a useful tool to allow early diagnosis of Turner syndrome

Normal bone health in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy

Fat Distribution and Lipid Profile of Young Adults with Congenital Adrenal Hyperplasia Due to 21‐Hydroxylase Enzyme Deficiency

Growth Curves for Girls with Turner Syndrome

Cardiovascular dysfunction risk in young adults with congenital adrenal hyperplasia caused by 21‐hydroxylase enzyme deficiency

Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia

Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density

A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins

Turner syndrome and metabolic derangements: Another example of fetal programming

Crescimento e composição corporal de uma coorte de crianças e adolescentes com diabetes tipo 1

Growth hormone effect on body composition in Turner syndrome

Impairment in Anthropometric Parameters and Body Composition in Females with Classical 21-Hydroxylase Deficiency

Clinical and laboratory profile of pediatric and adolescent patients with type 1 diabetes

Composição corporal em mulheres com deficiência da 21-hidroxilase: comparação dos métodos antropométricos e de impedância bioelétrica em relação a um grupo controle

A inclusão de novas técnicas de análise citogenética aperfeiçoou o diagnóstico cromossômico da síndrome de Turner

Bioelectrical Impedance Phase Angle and Its Determinants in Patients with Classic Congenital Adrenal Hyperplasia

Spontaneous final height in Turner's syndrome in Brazil

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