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Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factors.
Castanet M, Polak M, Bonaïti-Pellié C, Lyonnet S, Czernichow P, Léger J; AFDPHE (Association Française pour le Dépistage et la Prévention des Handicaps de l'Enfant). Castanet M, et al. Among authors: polak m. J Clin Endocrinol Metab. 2001 May;86(5):2009-14. doi: 10.1210/jcem.86.5.7501. J Clin Endocrinol Metab. 2001. PMID: 11344199
Familial forms of thyroid dysgenesis.
Castanet M, Polak M, Léger J. Castanet M, et al. Among authors: polak m. Endocr Dev. 2007;10:15-28. doi: 10.1159/000106817. Endocr Dev. 2007. PMID: 17684387 Review.
Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiency.
Chakhtoura Z, Bachelot A, Samara-Boustani D, Ruiz JC, Donadille B, Dulon J, Christin-Maître S, Bouvattier C, Raux-Demay MC, Bouchard P, Carel JC, Leger J, Kuttenn F, Polak M, Touraine P; Centre des Maladies Endocriniennes Rares de la Croissance and Association Surrénales. Chakhtoura Z, et al. Among authors: polak m. Eur J Endocrinol. 2008 Jun;158(6):879-87. doi: 10.1530/EJE-07-0887. Epub 2008 Apr 7. Eur J Endocrinol. 2008. PMID: 18390993
Epidemiology of thyroid dysgenesis: the familial component.
Castanet M, Marinovic D, Polak M, Léger J. Castanet M, et al. Among authors: polak m. Horm Res Paediatr. 2010;73(4):231-7. doi: 10.1159/000284386. Epub 2010 Mar 9. Horm Res Paediatr. 2010. PMID: 20215768 Review.
1,136 results