Bergadá, Ignacio

Steroid 21‐hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype–phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia

Marino, R., Ramirez, P., Galeano, J., Perez Garrido, N., Rocco, C., Ciaccio, M., Warman, D. M., Guercio, G., Chaler, E., Maceiras, M., et al. (2011) · Clinical Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 98

Cognitive profiles of patients with early detected and treated congenital hypothyroidism

Campos, M. L. P., Musso, M., Keselman, A. C., Gruñeiro, L., Bergadá, I., & Chiesa, A. E. (2017) · Archivos Argentinos de Pediatria

Thyroid Disorders and TreatmentsDown syndrome and intellectual disability research

Cited by 25

Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection

Braslavsky, D., Méndez, M. V., Prieto, L., Keselman, A., Enacan, R., Gruñeiro-Papendieck, L., Jullien, N., Savenau, A., Reynaud, R., Brue, T., et al. (2017) · Hormone Research in Paediatrics

Thyroid Disorders and TreatmentsMetabolism and Genetic Disorders

Cited by 19

Novel Insulin-Like Growth Factor 1 Gene Mutation: Broadening of the Phenotype and Implications for Insulin Resistance

Giacomozzi, C., Martin, A., Fernández, M. C., Gutiérrez, M., Iascone, M., Domené, H. M., Dominici, F. P., Bergadá, I., Cangiano, B., Persani, L., et al. (2023) · The Journal of Clinical Endocrinology & Metabolism

Growth Hormone and Insulin-like Growth FactorsGenomics and Rare Diseases

Cited by 10