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Thyroid : Official Journal of the American Thyroid Association|October 24, 2007
Thyroglobulin reference values in a pediatric infant populationGabriela Sobrero, Liliana Muñoz, Leonardo Bazzara, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 10, 2011
Vitamin D receptor genotypes are associated with bone mass in patients with Turner syndromeMaría Peralta López, Mirta Miras, Liliana Silvano, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|November 20, 2012
Association of vitamin D receptor gene Cdx2 polymorphism with bone markers in Turner syndrome patientsMaría Peralta López, Viviana Centeno, Mirta Miras, et al.Molecular and Cellular Endocrinology|May 10, 2023
The p.Cys1281Tyr variant in the hinge module/flap region of thyroglobulin causes intracellular transport disorder and congenital hypothyroidismMauricio Gomes Pio, Ezequiela Adrover, Mirta B Miras, et al.Molecular and Cellular Endocrinology|October 28, 2015
Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysisFiorella S Belforte, Cintia E Citterio, Graciela Testa, et al.The Journal of Clinical Endocrinology and Metabolism|May 14, 2011
Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5'-untranslated region in a patient with congenital hypothyroidismJuan Pablo Nicola, Magalí Nazar, Caroline Serrano-Nascimento, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2011
Comparative analysis of clinical, biochemical and genetic aspects associated with bone mineral density in small for gestational age childrenLiliana Silvano, Mirta Miras, Adriana Pérez, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 29, 2010
Serum levels of adiponectin and leptin in children born small for gestational age: relation to insulin sensitivity parametersMirta Miras, Mariana Ochetti, Silvia Martín, et al.Clinical Endocrinology|October 11, 2011
Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase geneFiorella S Belforte, Mirta B Miras, María C Olcese, et al.Frontiers in Endocrinology|May 23, 2022
Silent but Not Harmless: A Synonymous <i>SLC5A5</i> Gene Variant Leading to Dyshormonogenic Congenital HypothyroidismRomina Celeste Geysels, Carlos Eduardo Bernal Barquero, Mariano Martín, et al.Pageof 2