Stoupa, Athanasia

Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology

van Trotsenburg, P., Stoupa, A., Léger, J., Rohrer, T., Peters, C., Fugazzola, L., Cassio, A., Heinrichs, C., Beauloye, V., Pohlenz, J., et al. (2021) · Thyroid®

Thyroid Disorders and TreatmentsMetabolism and Genetic Disorders

Cited by 469

Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial

Groeneweg, S., Peeters, R. P., Moran, C., Stoupa, A., Auriol, F., Tonduti, D., Dica, A., Paone, L., Rozenkova, K., Malikova, J., et al. (2019) · The Lancet Diabetes & Endocrinology

Thyroid Disorders and TreatmentsMetabolism and Genetic Disorders

Cited by 129

TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology

Stoupa, A., Adam, F., Kariyawasam, D., Strassel, C., Gawade, S., Szinnai, G., Kauskot, A., Lasne, D., Janke, C., Natarajan, K., et al. (2018) · EMBO Molecular Medicine

Thyroid Disorders and TreatmentsGenetic and Kidney Cyst Diseases

Cited by 71

New genetics in congenital hypothyroidism

Stoupa, A., Kariyawasam, D., Muzza, M., de Filippis, T., Fugazzola, L., Polak, M., Persani, L., & Carré, A. (2021) · Endocrine

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 59

Update of Thyroid Developmental Genes

Stoupa, A., Kariyawasam, D., Carré, A., & Polak, M. (2016) · Endocrinology and Metabolism Clinics of North America

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 47

Inadequate cortisol response to the tetracosactide (Synacthen®) test in non-classic congenital adrenal hyperplasia: an exception to the rule

Stoupa, A., González-Briceño, L., Pinto, G., Samara-Boustani, D., Thalassinos, C., Flechtner, I., Beltrand, J., Bidet, M., Simon, A., Piketty, M., et al. (2015) · Hormone Research in Paediatrics

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 37

Thyroid Hypoplasia in Congenital Hypothyroidism Associated with Thyroid Peroxidase Mutations

Stoupa, A., Chaabane, R., Guériouz, M., Raynaud-Ravni, C., Nitschke, P., Bole-Feysot, C., Mnif, M., Ammar Keskes, L., Hachicha, M., Belguith, N., et al. (2018) · Thyroid

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 29

First case of fetal goitrous hypothyroidism due to SLC5A5/NIS mutations

Stoupa, A., Al Hage Chehade, G., Kariyawasam, D., Tohier, C., Bole-Feysot, C., Nitschke, P., Thibault, H., Jullie, M.-L., Polak, M., & Carré, A. (2020) · European Journal of Endocrinology

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 16