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Endocrine|August 27, 2011
Variable clinical presentation and outcome in pediatric patients with resistance to thyroid hormone (RTH)Ana Chiesa, Maria Cecilia Olcese, Patricia Papendieck, et al.
Archivos Argentinos De Pediatria|May 16, 2017
[Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases]Rosa E Enacán, María E Masnata, Fiorella Belforte, et al.
Plos One|May 8, 2025
Prevalent genetic alterations in pediatric thyroid carcinoma: Insights from an Argentinean studySandra Lorena Colli, Marisa Esther Boycho, Patricia Papendieck, et al.
International Journal of Molecular Sciences|August 26, 2022
Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport DefectCarlos Eduardo Bernal Barquero, Romina Celeste Geysels, Virginie Jacques, et al.
Molecular and Cellular Endocrinology|December 25, 2017
Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidismSofia Siffo, Ezequiela Adrover, Cintia E Citterio, et al.
Endocrine|May 4, 2022
Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesisMaricel F Molina, Patricia Papendieck, Gabriela Sobrero, et al.
Frontiers in Endocrinology|January 3, 2025
Functional characterization of novel compound heterozygous missense SLC5A5 gene variants causing congenital dyshormonogenic hypothyroidismGerardo Hernán Carro, Mariano Martín, Sofía Savy, et al.
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