Athanasia STOUPA | Institut Imagine

Presentation

Athanasia STOUPA

Molecular basis of several congenital or neonatal endocrine disorders and establishment of new therapeutic strategies

Contact :

athanasia.stoupa@institutimagine.org

About

Scientific Publications

Publications

2025

Digenic Inheritance Mode in Congenital Hypothyroidism Due to Thyroid Dysgenes..., J Clin Endocrinol Metab
2023

Borealin/CDCA8 deficiency alters thyroid development and results in papillary..., Front Endocrinol (Lausanne)
2019

Effectiveness and safety of the tri-iodothyronine analogue Triac in children ..., Lancet Diabetes Endocrinol
2018

TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet ph..., EMBO Mol Med
2018

Thyroid Hypoplasia in Congenital Hypothyroidism Associated with Thyroid Perox..., Thyroid
2016

Mutations in BOREALIN cause thyroid dysgenesis., Hum Mol Genet
2016

Update of Thyroid Developmental Genes., Endocrinol Metab Clin North Am