Fernanda A. Correa

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 15 publications

Hormone resistance and short stature: A journey through the pathways of hormone signaling.

Hormone resistance and short stature: A journey through the pathways of hormone signaling.

Journal: Molecular and cellular endocrinology

Published: January 15, 2021

Is There a Difference Between Minimal and Gross Extension into the Strap Muscles for the Risk of Recurrence in Papillary Thyroid Carcinomas?

Is There a Difference Between Minimal and Gross Extension into the Strap Muscles for the Risk of Recurrence in Papillary Thyroid Carcinomas?

Journal: Thyroid : official journal of the American Thyroid Association

Published: February 16, 2020

Update on new GH-IGF axis genetic defects.

Update on new GH-IGF axis genetic defects.

Journal: Archives of endocrinology and metabolism

Published: September 03, 2019

Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR.

Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR.

Journal: Endocrine connections

Published: March 21, 2019

Quality of Life and Coping in Multiple Endocrine Neoplasia Type 2.

Quality of Life and Coping in Multiple Endocrine Neoplasia Type 2.

Journal: Journal of the Endocrine Society

Published: November 09, 2018

Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery.

Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery.

Journal: Archives of endocrinology and metabolism

Published: April 03, 2018

Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes.

Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes.

Journal: Clinical endocrinology

Published: August 18, 2017

Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies.

Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies.

Journal: Journal of the Endocrine Society

Published: May 08, 2017

Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.

Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.

Journal: Clinical endocrinology

Published: March 05, 2017

Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing.

Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing.

Journal: Archives of endocrinology and metabolism

Published: February 11, 2016

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.

Journal: Endocrine connections

Published: March 05, 2015

A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).

A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).

Journal: European journal of endocrinology

Published: February 09, 2015

Showing 1-12 of 15

Last Updated: 09/26/2026