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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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Repurposing Saquinavir for Host-Directed Therapy to Control Mycobacterium Tuberculosis Infection

Frontiers in immunology, 2021-03, Vol.12, p.647728

2021

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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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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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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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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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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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Dies1/VISTA expression loss is a recurrent event in gastric cancer due to epigenetic regulation

Scientific reports, 2016-10, Vol.6 (1), p.34860-34860, Article 34860

2016

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Higher Body Fat but Similar Phase Angle Values in Patients with the Classical Form of Congenital Adrenal Hyperplasia in Comparison to a Control Group

Nutrients, 2022-12, Vol.14 (23), p.5184

2022

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Trauma Associado às Touradas à Corda nos Açores: Um Estudo Transversal

Acta médica portuguesa, 2024-04

2024

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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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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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Determinants of Audit Fees for Portugal and Spain

Contaduría, administración, 2020-12, Vol.65 (4), p.193

2020

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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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Coastal climate adaptation in port-cities: adaptation deficits, barriers, and challenges ahead

Journal of environmental planning and management, 2020-02, Vol.63 (3), p.389-414

2020

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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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Advances in immunotherapy for breast cancer and feline mammary carcinoma: From molecular basis to novel therapeutic targets

Biochimica et biophysica acta. Reviews on cancer, 2024-09, Vol.1879 (5), p.189144, Article 189144

2024

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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 (2016), p.509-518-057

2016

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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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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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Compositional and microstructural effects in composite electrolytes for fuel cells

International journal of energy research, 2011-10, Vol.35 (12), p.1090-1099

2011

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

Archives of Endocrinology and Metabolism, 2024-01, Vol.68

2024

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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

Repurposing Saquinavir for Host-Directed Therapy to Control Mycobacterium Tuberculosis Infection

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

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

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

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

Systematic review of quality of life in Turner syndrome

Dies1/VISTA expression loss is a recurrent event in gastric cancer due to epigenetic regulation

Higher Body Fat but Similar Phase Angle Values in Patients with the Classical Form of Congenital Adrenal Hyperplasia in Comparison to a Control Group

Trauma Associado às Touradas à Corda nos Açores: Um Estudo Transversal

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

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

Determinants of Audit Fees for Portugal and Spain

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

Coastal climate adaptation in port-cities: adaptation deficits, barriers, and challenges ahead

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

Advances in immunotherapy for breast cancer and feline mammary carcinoma: From molecular basis to novel therapeutic targets

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

Growth Curves for Girls with Turner Syndrome

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

Compositional and microstructural effects in composite electrolytes for fuel cells

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

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

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