Flavia A. Barbosa-Costa

Sao Paulo, SP 04077020, Brazil

Last Updated: 09/26/2026

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Found 14 publications

Skeletal Microstructure in Addison's Disease.

Skeletal Microstructure in Addison's Disease.

Journal: Journal of the Endocrine Society

Published: September 28, 2025

Delayed Bone Maturation and Extended Growth Phase as Distinctive Features of 17α-Hydroxylase/17,20-Lyase Deficiency: A Retro-Prospective Study of a Large Patient Cohort.

Delayed Bone Maturation and Extended Growth Phase as Distinctive Features of 17α-Hydroxylase/17,20-Lyase Deficiency: A Retro-Prospective Study of a Large Patient Cohort.

Journal: Clinical endocrinology

Published: October 08, 2024

Successful Pregnancy in Isolated 17,20-lyase Deficiency Without Glucocorticoid Use or Assisted Reproduction Techniques.

Successful Pregnancy in Isolated 17,20-lyase Deficiency Without Glucocorticoid Use or Assisted Reproduction Techniques.

Journal: JCEM case reports

Published: January 23, 2024

Pheochromocytoma/Paraganglioma (PPGL): A Misdiagnosed Cause of Hypertension during Pregnancy.

Pheochromocytoma/Paraganglioma (PPGL): A Misdiagnosed Cause of Hypertension during Pregnancy.

Journal: Case reports in obstetrics and gynecology

Published: August 13, 2023

Focus on adrenal and related causes of hypertension in childhood and adolescence: Rare or rarely recognized?

Focus on adrenal and related causes of hypertension in childhood and adolescence: Rare or rarely recognized?

Journal: Archives of endocrinology and metabolism

Published: August 05, 2022

Classic and current concepts in adrenal steroidogenesis: a reappraisal.

Classic and current concepts in adrenal steroidogenesis: a reappraisal.

Journal: Archives of endocrinology and metabolism

Published: March 09, 2022

Reassessment of predictive values of ACTH-stimulated serum 21-deoxycortisol and 17-hydroxyprogesterone to identify CYP21A2 heterozygote carriers and nonclassic subjects.

Reassessment of predictive values of ACTH-stimulated serum 21-deoxycortisol and 17-hydroxyprogesterone to identify CYP21A2 heterozygote carriers and nonclassic subjects.

Journal: Clinical endocrinology

Published: March 23, 2021

Spontaneous fertility and variable spectrum of reproductive phenotype in a family with adult-onset X-linked adrenal insufficiency harboring a novel DAX-1/NR0B1 mutation.

Spontaneous fertility and variable spectrum of reproductive phenotype in a family with adult-onset X-linked adrenal insufficiency harboring a novel DAX-1/NR0B1 mutation.

Journal: BMC endocrine disorders

Published: November 24, 2019

Saliva versus serum cortisol to identify subclinical hypercortisolism in adrenal incidentalomas: simplicity versus accuracy.

Saliva versus serum cortisol to identify subclinical hypercortisolism in adrenal incidentalomas: simplicity versus accuracy.

Journal: Journal of endocrinological investigation

Published: March 05, 2019

Cyclic Subclinical Hypercortisolism: A Previously Unidentified Hypersecretory Form of Adrenal Incidentalomas.

Cyclic Subclinical Hypercortisolism: A Previously Unidentified Hypersecretory Form of Adrenal Incidentalomas.

Journal: Journal of the Endocrine Society

Published: November 21, 2018

A novel GNRHR gene mutation causing congenital hypogonadotrophic hypogonadism in a Brazilian kindred.

A novel GNRHR gene mutation causing congenital hypogonadotrophic hypogonadism in a Brazilian kindred.

Journal: Journal of neuroendocrinology

Published: October 01, 2018

Confounder factors masking a Leydig-cell ovarian tumor in a post-menopausal woman treated for androgen-positive receptor breast cancer.

Confounder factors masking a Leydig-cell ovarian tumor in a post-menopausal woman treated for androgen-positive receptor breast cancer.

Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Published: April 27, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026