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Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue.
Rochette C, Jullien N, Saveanu A, Caldagues E, Bergada I, Braslavsky D, Pfeifer M, Reynaud R, Herman JP, Barlier A, Brue T, Enjalbert A, Castinetti F. Rochette C, et al. Among authors: enjalbert a. PLoS One. 2015 May 8;10(5):e0126648. doi: 10.1371/journal.pone.0126648. eCollection 2015. PLoS One. 2015. PMID: 25955177 Free PMC article.
Congenital pituitary hormone deficiencies: role of LHX3/LHX4 genes.
Castinetti F, Reynaud R, Saveanu A, Quentien MH, Albarel F, Enjalbert A, Barlier A, Brue T. Castinetti F, et al. Among authors: enjalbert a. Expert Rev Endocrinol Metab. 2008 Nov;3(6):751-760. doi: 10.1586/17446651.3.6.751. Expert Rev Endocrinol Metab. 2008. PMID: 30764064
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.
Vallette-Kasic S, Barlier A, Teinturier C, Diaz A, Manavela M, Berthezène F, Bouchard P, Chaussain JL, Brauner R, Pellegrini-Bouiller I, Jaquet P, Enjalbert A, Brue T. Vallette-Kasic S, et al. Among authors: enjalbert a. J Clin Endocrinol Metab. 2001 Sep;86(9):4529-35. doi: 10.1210/jcem.86.9.7811. J Clin Endocrinol Metab. 2001. PMID: 11549703
[Clinical and genetic aspects of combined pituitary hormone deficiencies].
Castinetti F, Reynaud R, Saveanu A, Quentien MH, Albarel F, Barlier A, Enjalbert A, Brue T. Castinetti F, et al. Among authors: enjalbert a. Ann Endocrinol (Paris). 2008 Feb;69(1):7-17. doi: 10.1016/j.ando.2008.01.001. Epub 2008 Mar 4. Ann Endocrinol (Paris). 2008. PMID: 18291347 Review. French.
351 results