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Page 1
Molecular mechanisms of thyroid dysgenesis.
Polak M, Sura-Trueba S, Chauty A, Szinnai G, Carré A, Castanet M. Polak M, et al. Among authors: carre a. Horm Res. 2004;62 Suppl 3:14-21. doi: 10.1159/000080494. Horm Res. 2004. PMID: 15539794 Review.
Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndrome.
Teissier R, Guillot L, Carré A, Morandini M, Stuckens C, Ythier H, Munnich A, Szinnai G, de Blic J, Clement A, Leger J, Castanet M, Epaud R, Polak M. Teissier R, et al. Among authors: carre a. Horm Res Paediatr. 2012;77(3):146-51. doi: 10.1159/000337214. Epub 2012 Apr 5. Horm Res Paediatr. 2012. PMID: 22488412
Thyroid function in fetuses with down syndrome.
Luton D, Azria E, Polak M, Carré A, Vuillard E, Delezoide AL, Guibourdenche J. Luton D, et al. Among authors: carre a. Horm Res Paediatr. 2012;78(2):88-93. doi: 10.1159/000341149. Epub 2012 Aug 14. Horm Res Paediatr. 2012. PMID: 22907384
Update of Thyroid Developmental Genes.
Stoupa A, Kariyawasam D, Carré A, Polak M. Stoupa A, et al. Among authors: carre a. Endocrinol Metab Clin North Am. 2016 Jun;45(2):243-54. doi: 10.1016/j.ecl.2016.01.007. Epub 2016 Apr 13. Endocrinol Metab Clin North Am. 2016. PMID: 27241962 Review.
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 ML, Polak M, Carré A. Stoupa A, et al. Among authors: carre a. Eur J Endocrinol. 2020 Nov;183(5):K1-K5. doi: 10.1530/EJE-20-0255. Eur J Endocrinol. 2020. PMID: 32805706
New genetics in congenital hypothyroidism.
Stoupa A, Kariyawasam D, Muzza M, de Filippis T, Fugazzola L, Polak M, Persani L, Carré A. Stoupa A, et al. Among authors: carre a. Endocrine. 2021 Mar;71(3):696-705. doi: 10.1007/s12020-021-02646-9. Epub 2021 Mar 1. Endocrine. 2021. PMID: 33650047 Review.
292 results