Mirta B. Miras

Cordoba, X, Argentina

Last Updated: 09/26/2026

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Found 20 publications

Reference values for anti-Müllerian hormone measured by electrochemiluminescence in a pediatric population in Argentina.

Reference values for anti-Müllerian hormone measured by electrochemiluminescence in a pediatric population in Argentina.

Journal: Archivos argentinos de pediatria

Published: July 01, 2025

Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate Genes.

Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate Genes.

Journal: The Journal of clinical endocrinology and metabolism

Published: February 08, 2024

Knockout mice with pituitary malformations help identify human cases of hypopituitarism.

Knockout mice with pituitary malformations help identify human cases of hypopituitarism.

Journal: Genome medicine

Published: October 09, 2023

The p.Cys1281Tyr variant in the hinge module/flap region of thyroglobulin causes intracellular transport disorder and congenital hypothyroidism.

The p.Cys1281Tyr variant in the hinge module/flap region of thyroglobulin causes intracellular transport disorder and congenital hypothyroidism.

Journal: Molecular and cellular endocrinology

Published: March 20, 2023

Silent but Not Harmless: A Synonymous SLC5A5 Gene Variant Leading to Dyshormonogenic Congenital Hypothyroidism.

Silent but Not Harmless: A Synonymous SLC5A5 Gene Variant Leading to Dyshormonogenic Congenital Hypothyroidism.

Journal: Frontiers in endocrinology

Published: February 03, 2022

Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis.

Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis.

Journal: Endocrine

Published: January 07, 2022

A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.

A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.

Journal: The Journal of clinical endocrinology and metabolism

Published: January 07, 2021

Neonatal and Infant Reference Intervals for FSH, LH, Testosterone, Estradiol, Cortisol and DHEA-S by Electrochemiluminescence in Argentina.

Neonatal and Infant Reference Intervals for FSH, LH, Testosterone, Estradiol, Cortisol and DHEA-S by Electrochemiluminescence in Argentina.

Journal: Pediatric endocrinology reviews : PER

Published: August 03, 2020

Statement of Argentine pediatric endocrinologists on growth hormone interchangeability.

Statement of Argentine pediatric endocrinologists on growth hormone interchangeability.

Journal: Archivos argentinos de pediatria

Published: July 25, 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

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism.

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism.

Journal: Molecular and cellular endocrinology

Published: September 06, 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

Showing 1-12 of 20

Last Updated: 09/26/2026