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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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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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Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with Its Development in Congenital Adrenal Hyperplasia

Hormone research in paediatrics, 2018-01, Vol.90 (3), p.161-168

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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Growth Curves for Girls with Turner Syndrome

BioMed research international, 2014-01, Vol.2014 (2014), p.1-8

2014

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Accuracy of anthropometric measurements in estimating fat mass in individuals with 21-hydroxylase deficiency

Nutrition (Burbank, Los Angeles County, Calif.), 2012-10, Vol.28 (10), p.984-990

2012

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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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Social skills in women with Turner Syndrome

Scandinavian journal of psychology, 2011-10, Vol.52 (5), p.440-447

2011

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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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Growth hormone effect on body composition in Turner syndrome

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

2011

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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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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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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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Spontaneous puberty in girls with early diagnosis of Turner syndrome

Arquivos brasileiros de endocrinologia e metabologia, 2012-12, Vol.56 (9), p.653-657

2012

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Insights from a Wolfram syndrome cohort: clinical and molecular findings from a specialized diabetes reference center

Archives of endocrinology and metabolism, 2024, Vol.68, p.e240091

2024

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Spontaneous final height in Turner's syndrome in Brazil

Journal of Pediatric Endocrinology and Metabolism, 2007-11, Vol.20 (11), p.1207

2007

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Growth and body composition of a cohort of children and adolescents with type 1 diabetes

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

2013

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Metabolic evaluation of young women with congenital adrenal hyperplasia

Arquivos brasileiros de endocrinologia e metabologia, 2011-11, Vol.55 (8), p.646-652

2011

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The inclusion of new techniques of chromosome analysis has improved the cytogenetic profile of Turner syndrome

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

2009

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Body composition in females with 21-hydroxylase deficiency: comparison of anthropometric methods and bioelectric impedance in relation to a control group

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

2010

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Turner's syndrome and thyroid disease: a transverse study of pediatric patients in Brazil

Journal of Pediatric Endocrinology and Metabolism, 2000-04, Vol.13 (4), p.357

2000

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True hermaphrodites in the southeastern region of Brazil: a different cytogenetic and gonadal profile

Journal of Pediatric Endocrinology and Metabolism, 1998-07, Vol.11 (4), p.519

1998

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Cardiovascular and renal anomalies in Turner syndrome

Revista da Associacao Medica Brasileira (1992), 2010-11, Vol.56 (6), p.655-659

2010

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Prenatal Diagnosis of Aberrant Right Subclavian Artery: Association with Genetic Abnormalities

Revista Brasileira de ginecologia e obstetrícia, 2021-06, Vol.43 (6), p.452-456

2021

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Microbleeds and cavernomas after radiotherapy for paediatric primary brain tumours

Journal of the neurological sciences, 2017-01, Vol.372, p.413-416

2017

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

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

Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with Its Development in Congenital Adrenal Hyperplasia

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

Growth Curves for Girls with Turner Syndrome

Accuracy of anthropometric measurements in estimating fat mass in individuals with 21-hydroxylase deficiency

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

Social skills in women with Turner Syndrome

Turner syndrome and metabolic derangements: Another example of fetal programming

Growth hormone effect on body composition in Turner syndrome

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

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

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

Spontaneous puberty in girls with early diagnosis of Turner syndrome

Insights from a Wolfram syndrome cohort: clinical and molecular findings from a specialized diabetes reference center

Spontaneous final height in Turner's syndrome in Brazil

Growth and body composition of a cohort of children and adolescents with type 1 diabetes

Metabolic evaluation of young women with congenital adrenal hyperplasia

The inclusion of new techniques of chromosome analysis has improved the cytogenetic profile of Turner syndrome

Body composition in females with 21-hydroxylase deficiency: comparison of anthropometric methods and bioelectric impedance in relation to a control group

Turner's syndrome and thyroid disease: a transverse study of pediatric patients in Brazil

True hermaphrodites in the southeastern region of Brazil: a different cytogenetic and gonadal profile

Cardiovascular and renal anomalies in Turner syndrome

Prenatal Diagnosis of Aberrant Right Subclavian Artery: Association with Genetic Abnormalities

Microbleeds and cavernomas after radiotherapy for paediatric primary brain tumours

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