Catherine Voutetakis-Dacou

Athens, ESYE31, Greece

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Prenatal stress, hormones, and fetal brain development: gender differences.

Prenatal stress, hormones, and fetal brain development: gender differences.

Journal: Hormones (Athens, Greece)

Published: April 20, 2025

HNF1A gene mutations and premature ovarian failure (POF): evidence from a clinical paradigm combining MODY 3 and POF.

HNF1A gene mutations and premature ovarian failure (POF): evidence from a clinical paradigm combining MODY 3 and POF.

Journal: Hormones (Athens, Greece)

Published: November 06, 2023

Molecular Analysis of the CYP11B2 Gene in 62 Patients with Hypoaldosteronism Due to Aldosterone Synthase Deficiency.

Molecular Analysis of the CYP11B2 Gene in 62 Patients with Hypoaldosteronism Due to Aldosterone Synthase Deficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 20, 2020

Long-term outcome of differentiated thyroid cancer in children and young adults: risk stratification by ATA criteria and assessment of pre-ablation stimulated thyroglobulin as predictors of disease persistence.

Long-term outcome of differentiated thyroid cancer in children and young adults: risk stratification by ATA criteria and assessment of pre-ablation stimulated thyroglobulin as predictors of disease persistence.

Journal: Endocrine

Published: March 27, 2020

Adrenal Steroids in Female Hypothyroid Neonates: Unraveling an Association Between Thyroid Hormones and Adrenal Remodeling.

Adrenal Steroids in Female Hypothyroid Neonates: Unraveling an Association Between Thyroid Hormones and Adrenal Remodeling.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 17, 2018

Pituitary stalk interruption syndrome: cause, clinical manifestations, diagnosis, and management.

Pituitary stalk interruption syndrome: cause, clinical manifestations, diagnosis, and management.

Journal: Current opinion in pediatrics

Published: July 09, 2016

A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis-ptosis-epicanthus inversus syndrome.

A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis-ptosis-epicanthus inversus syndrome.

Journal: Menopause (New York, N.Y.)

Published: May 20, 2015

The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene.

The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene.

Journal: Clinical endocrinology

Published: April 22, 2014

Central precocious puberty in a girl and early puberty in her brother caused by a novel mutation in the MKRN3 gene.

Central precocious puberty in a girl and early puberty in her brother caused by a novel mutation in the MKRN3 gene.

Journal: The Journal of clinical endocrinology and metabolism

Published: January 21, 2014

Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes.

Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes.

Journal: The Journal of clinical endocrinology and metabolism

Published: March 12, 2013

CYP21A2 mutations in women with polycystic ovary syndrome (PCOS).

CYP21A2 mutations in women with polycystic ovary syndrome (PCOS).

Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme

Published: February 07, 2013

The spectrum of HNF1A gene mutations in Greek patients with MODY3: relative frequency and identification of seven novel germline mutations.

The spectrum of HNF1A gene mutations in Greek patients with MODY3: relative frequency and identification of seven novel germline mutations.

Journal: Pediatric diabetes

Published: December 06, 2012

Showing 1-12 of 15

Last Updated: 09/26/2026