Publications by authors named "Graciela Testa"

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Nocturnal Salivary Cortisol Is an Accurate Non-Invasive Test to Assess Endogenous Hypercortisolism in Children with Obesity and a Clinical Phenotype Suspicious for Cushing's Syndrome.
María Gabriela Ballerini, María Gabriela Ballerini, Analía Verónica Freire, María Eugenia Rodríguez, Luciana Brenzoni, Graciela Testa

Horm Res Paediatr· December 2025

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Silent but Not Harmless: A Synonymous Gene Variant Leading to Dyshormonogenic Congenital Hypothyroidism.
Romina Celeste Geysels, Carlos Eduardo Bernal Barquero, Mariano Martín, Victoria Peyret, Martina Nocent, Graciela Testa

Front Endocrinol (Lausanne)· May 2022

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A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.
Mariano Martín, Carlos Pablo Modenutti, Mauco Lucas Gil Rosas, Victoria Peyret, Romina Celeste Geysels, Graciela Testa

J Clin Endocrinol Metab· June 2021

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Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis.
Fiorella S Belforte, Cintia E Citterio, Graciela Testa, María Cecilia Olcese, Gabriela Sobrero

Mol Cell Endocrinol· January 2016

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Measurement of Serum 17α-Hydroxyprogesterone in Infants by Radioimmunoassay.
Liliana Noemi Muñoz, Mariana Ochetti, Gonzalo Perez, Gabriela Maria Sobrero, Liliana Karina Silvano, Graciela María Testa

Pediatr Endocrinol Rev· June 2015

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New insights into thyroglobulin gene: molecular analysis of seven novel mutations associated with goiter and hypothyroidism.
Cintia E Citterio, Gloria A Machiavelli, Mirta B Miras, Laura Gruñeiro-Papendieck, Katherine Lachlan, Graciela Testa

Mol Cell Endocrinol· January 2013

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Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene.
Fiorella S Belforte, Mirta B Miras, María C Olcese, Gabriela Sobrero, Graciela Testa

Clin Endocrinol (Oxf)· April 2012

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Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5'-untranslated region in a patient with congenital hypothyroidism.
Juan Pablo Nicola, Magalí Nazar, Caroline Serrano-Nascimento, Francemilson Goulart-Silva, Gabriela Sobrero, Graciela Testa

J Clin Endocrinol Metab· July 2011

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