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Frontiers in Endocrinology|September 6, 2021
Update on Neonatal Isolated Hyperthyrotropinemia: A Systematic ReviewAna E Chiesa, Mariana L Tellechea
Congenital Heart Disease|April 28, 2012
Spontaneous termination of ventricular fibrillation in a patient with congenital coronary anomalyOscar A Pellizzón, Lorena Scaglione, Ana E Chiesa, 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.
Frontiers in Endocrinology|November 20, 2025
Variation spectra in mild isolated hyperthyrotropinemia: pilot cohort and systematic reviewValentina Ricci, María E Masnata, María D Villanueva Gonzalez, et al.
American Journal of Human Genetics|July 16, 2020
The Genetic Landscape and Epidemiology of PhenylketonuriaAlicia Hillert, Yair Anikster, Amaya Belanger-Quintana, et al.
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