Polak M - Search Results

1

Stoupa A, Kariyawasam D, Polak M, Carré A. Stoupa A, et al. Among authors: polak m. Med Sci (Paris). 2022 Mar;38(3):263-273. doi: 10.1051/medsci/2022028. Epub 2022 Mar 25. Med Sci (Paris). 2022. PMID: 35333163 Free article. French.

2

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

3

Thyroid developmental anomalies in first degree relatives of children with congenital hypothyroidism.

Léger J, Marinovic D, Garel C, Bonaïti-Pellié C, Polak M, Czernichow P. Léger J, et al. Among authors: polak m. J Clin Endocrinol Metab. 2002 Feb;87(2):575-80. doi: 10.1210/jcem.87.2.8268. J Clin Endocrinol Metab. 2002. PMID: 11836288

4

A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate.

Castanet M, Park SM, Smith A, Bost M, Léger J, Lyonnet S, Pelet A, Czernichow P, Chatterjee K, Polak M. Castanet M, et al. Among authors: polak m. Hum Mol Genet. 2002 Aug 15;11(17):2051-9. doi: 10.1093/hmg/11.17.2051. Hum Mol Genet. 2002. PMID: 12165566

5

Molecular mechanisms of thyroid dysgenesis.

Polak M, Sura-Trueba S, Chauty A, Szinnai G, Carré A, Castanet M. Polak M, et al. Horm Res. 2004;62 Suppl 3:14-21. doi: 10.1159/000080494. Horm Res. 2004. PMID: 15539794 Review.

6

Linkage and mutational analysis of familial thyroid dysgenesis demonstrate genetic heterogeneity implicating novel genes.

Castanet M, Sura-Trueba S, Chauty A, Carré A, de Roux N, Heath S, Léger J, Lyonnet S, Czernichow P, Polak M. Castanet M, et al. Among authors: polak m. Eur J Hum Genet. 2005 Feb;13(2):232-9. doi: 10.1038/sj.ejhg.5201321. Eur J Hum Genet. 2005. PMID: 15547625

7

[Hypothyroidism in child].

Polak M. Polak M. Rev Prat. 2005 Dec 15;55(19):2173-80. Rev Prat. 2005. PMID: 16544929 Review. French. No abstract available.

8

[Congenital hypothyroidism].

Carranza D, Van Vliet G, Polak M. Carranza D, et al. Among authors: polak m. Ann Endocrinol (Paris). 2006 Sep;67(4):295-302. doi: 10.1016/s0003-4266(06)72601-4. Ann Endocrinol (Paris). 2006. PMID: 17072233 Review. French.

9

Sodium/iodide symporter (NIS) gene expression is the limiting step for the onset of thyroid function in the human fetus.

Szinnai G, Lacroix L, Carré A, Guimiot F, Talbot M, Martinovic J, Delezoide AL, Vekemans M, Michiels S, Caillou B, Schlumberger M, Bidart JM, Polak M. Szinnai G, et al. Among authors: polak m. J Clin Endocrinol Metab. 2007 Jan;92(1):70-6. doi: 10.1210/jc.2006-1450. Epub 2006 Oct 31. J Clin Endocrinol Metab. 2007. PMID: 17077129

10

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.

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