Romina G. Armando

Center For Endocrinological Research 'Dr. César Bergadá'
B, Argentina

Last Updated: 09/26/2026

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Found 19 publications

MCT8 Deficiency in Two Brothers With a Novel Deletion Mutation in SLC16A2.

MCT8 Deficiency in Two Brothers With a Novel Deletion Mutation in SLC16A2.

Journal: Case reports in genetics

Published: August 28, 2025

Improving therapeutic strategies for triple-negative breast cancer: synergistic effects of DKC1 inhibition and paclitaxel.

Improving therapeutic strategies for triple-negative breast cancer: synergistic effects of DKC1 inhibition and paclitaxel.

Journal: Expert opinion on therapeutic targets

Published: July 21, 2025

CADD-based discovery of novel oligomeric modulators of PKM2 with antitumor activity in aggressive human glioblastoma models.

CADD-based discovery of novel oligomeric modulators of PKM2 with antitumor activity in aggressive human glioblastoma models.

Journal: Heliyon

Published: October 29, 2024

Extreme Phenotypic Variability of ACTG1-Related Disorders in Hearing Loss.

Extreme Phenotypic Variability of ACTG1-Related Disorders in Hearing Loss.

Journal: Advanced genetics (Hoboken, N.J.)

Published: August 09, 2024

Non-syndromic Hirschsprung's disease as a result of a RET gene variant.

Non-syndromic Hirschsprung's disease as a result of a RET gene variant.

Journal: Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica

Published: April 16, 2024

Key role of PIN1 in telomere maintenance and oncogenic behavior in a human glioblastoma model.

Key role of PIN1 in telomere maintenance and oncogenic behavior in a human glioblastoma model.

Journal: Oncology reports

Published: October 20, 2022

In vitro characterization and rational analog design of a novel inhibitor of telomerase assembly in MDA MB 231 breast cancer cell line.

In vitro characterization and rational analog design of a novel inhibitor of telomerase assembly in MDA MB 231 breast cancer cell line.

Journal: Oncology reports

Published: May 13, 2022

Late diagnosis of spinal muscular atrophy in a patient with Down syndrome

Late diagnosis of spinal muscular atrophy in a patient with Down syndrome

Journal: Archivos argentinos de pediatria

Published: December 30, 2021

Rational design of PIN1 inhibitors for cancer treatment based on conformational diversity analysis and docking based virtual screening.

Rational design of PIN1 inhibitors for cancer treatment based on conformational diversity analysis and docking based virtual screening.

Journal: Journal of biomolecular structure & dynamics

Published: January 19, 2021

Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.

Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.

Journal: Molecular biology reports

Published: February 03, 2020

New drugs are not enough‑drug repositioning in oncology: An update.

New drugs are not enough‑drug repositioning in oncology: An update.

Journal: International journal of oncology

Published: August 15, 2019

A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.

A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.

Journal: European journal of endocrinology

Published: July 19, 2019

Showing 1-12 of 19

Last Updated: 09/26/2026