Antonella Fabretto

Trieste, Italy

Last Updated: 09/26/2026

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Found 16 publications

Adrenal Biomarkers of Stress in Transgender and Gender-Diverse Adolescents.

Adrenal Biomarkers of Stress in Transgender and Gender-Diverse Adolescents.

Journal: Developmental psychobiology

Published: September 20, 2025

Two-year real-world experience with somatrogon in children and adolescents with growth hormone deficiency.

Two-year real-world experience with somatrogon in children and adolescents with growth hormone deficiency.

Journal: Frontiers in endocrinology

Published: August 14, 2025

Preanalytical Stability of 13 Antibiotics in Biological Samples: A Crucial Factor for Therapeutic Drug Monitoring.

Preanalytical Stability of 13 Antibiotics in Biological Samples: A Crucial Factor for Therapeutic Drug Monitoring.

Journal: Antibiotics (Basel, Switzerland)

Published: July 01, 2024

Prevalence and characteristics of thelarche variant.

Prevalence and characteristics of thelarche variant.

Journal: Frontiers in endocrinology

Published: September 28, 2023

A Validated HPLC-Diode Array Detection Method for Therapeutic Drug Monitoring of Thiopurines in Pediatric Patients: From Bench to Bedside.

A Validated HPLC-Diode Array Detection Method for Therapeutic Drug Monitoring of Thiopurines in Pediatric Patients: From Bench to Bedside.

Journal: Metabolites

Published: October 29, 2022

Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate.

Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate.

Journal: Molecular genetics & genomic medicine

Published: July 25, 2019

Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysis.

Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysis.

Journal: Molecular genetics & genomic medicine

Published: September 27, 2018

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.

Journal: Nature communications

Published: July 30, 2018

A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome.

A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome.

Journal: Neurocase

Published: July 04, 2018

19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference.

19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference.

Journal: European journal of human genetics : EJHG

Published: January 22, 2017

CTNND2 deletion and intellectual disability.

CTNND2 deletion and intellectual disability.

Journal: Gene

Published: November 25, 2014

Severe inflammatory bowel disease associated with congenital alteration of transforming growth factor beta signaling.

Severe inflammatory bowel disease associated with congenital alteration of transforming growth factor beta signaling.

Journal: Journal of Crohn's & colitis

Published: September 12, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026