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Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.
Fournet JC, Mayaud C, de Lonlay P, Gross-Morand MS, Verkarre V, Castanet M, Devillers M, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C. Fournet JC, et al. Among authors: castanet m. Am J Pathol. 2001 Jun;158(6):2177-84. doi: 10.1016/S0002-9440(10)64689-5. Am J Pathol. 2001. PMID: 11395395 Free PMC article.
[Munchausen syndrome by proxy].
Bocquet N, Boileau P, Castanet M, Gautier I, Lamboley G, Richard E, de Tournemire R, Saudubray JM. Bocquet N, et al. Among authors: castanet m. Arch Pediatr. 1997 Aug;4(8):770-8. doi: 10.1016/s0929-693x(97)83421-5. Arch Pediatr. 1997. PMID: 9337903 Review. French.
Molecular mechanisms of thyroid dysgenesis.
Polak M, Sura-Trueba S, Chauty A, Szinnai G, Carré A, Castanet M. Polak M, et al. Among authors: castanet m. Horm Res. 2004;62 Suppl 3:14-21. doi: 10.1159/000080494. Horm Res. 2004. PMID: 15539794 Review.
Familial forms of thyroid dysgenesis.
Castanet M, Polak M, Léger J. Castanet M, et al. Endocr Dev. 2007;10:15-28. doi: 10.1159/000106817. Endocr Dev. 2007. PMID: 17684387 Review.
Congenital hyperthyroidism: the fetus as a patient.
Polak M, Legac I, Vuillard E, Guibourdenche J, Castanet M, Luton D. Polak M, et al. Among authors: castanet m. Horm Res. 2006;65(5):235-42. doi: 10.1159/000092454. Epub 2006 Mar 30. Horm Res. 2006. PMID: 16582565 Review.
66 results