Barlier A - Search Results

1

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency.

Jullien N, Romanet P, Philippon M, Quentien MH, Beck-Peccoz P, Bergada I, Odent S, Reynaud R, Barlier A, Saveanu A, Brue T, Castinetti F. Jullien N, et al. Among authors: barlier a. Eur J Hum Genet. 2019 Feb;27(2):216-225. doi: 10.1038/s41431-018-0264-6. Epub 2018 Sep 27. Eur J Hum Genet. 2019. PMID: 30262920 Free PMC article.

2

A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency.

Pellegrini-Bouiller I, Bélicar P, Barlier A, Gunz G, Charvet JP, Jaquet P, Brue T, Vialettes B, Enjalbert A. Pellegrini-Bouiller I, et al. Among authors: barlier a. J Clin Endocrinol Metab. 1996 Aug;81(8):2790-6. doi: 10.1210/jcem.81.8.8768831. J Clin Endocrinol Metab. 1996. PMID: 8768831

3

Prolactinomas resistant to bromocriptine: long-term efficacy of quinagolide and outcome of pregnancy.

Morange I, Barlier A, Pellegrini I, Brue T, Enjalbert A, Jaquet P. Morange I, et al. Among authors: barlier a. Eur J Endocrinol. 1996 Oct;135(4):413-20. doi: 10.1530/eje.0.1350413. Eur J Endocrinol. 1996. PMID: 8921822

4

[Evaluation of an immunoradiometric assay for succinylated ACTH].

Saveanu A, Barlier A, De Boissezon C, Kertesz G, Jean F, Argémi B, Cailla H, Jaquet P. Saveanu A, et al. Among authors: barlier a. Ann Endocrinol (Paris). 1999 Nov;60(5):414-21. Ann Endocrinol (Paris). 1999. PMID: 10615521 French.

5

[Pituitary development and pathology of transcription factors].

Barlier A, Vallette-Kasic S, Manavela M, Perez M, Diaz A, Pellegrini-Bouiller I, Enjalbert A, Brue T. Barlier A, et al. Ann Endocrinol (Paris). 2000 Sep;61(3):201-7. Ann Endocrinol (Paris). 2000. PMID: 10970945 Review. French.

6

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: barlier 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

7

[Congenital hypopituitarism: when should transcription factor gene screenings be performed?].

Reynaud R, Barlier A, Chadli-Chaieb M, Saveanu A, Simonin G, Enjalbert A, Brue T. Reynaud R, et al. Among authors: barlier a. Presse Med. 2004 Mar 27;33(6):400-5. doi: 10.1016/s0755-4982(04)98607-1. Presse Med. 2004. PMID: 15105786 Review. French.

8

Pituitary hormone deficiencies due to transcription factor gene alterations.

Reynaud R, Saveanu A, Barlier A, Enjalbert A, Brue T. Reynaud R, et al. Among authors: barlier a. Growth Horm IGF Res. 2004 Dec;14(6):442-8. doi: 10.1016/j.ghir.2004.07.001. Growth Horm IGF Res. 2004. PMID: 15519252 Review.

9

A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies.

Reynaud R, Chadli-Chaieb M, Vallette-Kasic S, Barlier A, Sarles J, Pellegrini-Bouiller I, Enjalbert A, Chaieb L, Brue T. Reynaud R, et al. Among authors: barlier a. J Clin Endocrinol Metab. 2004 Nov;89(11):5779-86. doi: 10.1210/jc.2003-032124. J Clin Endocrinol Metab. 2004. PMID: 15531542

10

Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.

Vallette-Kasic S, Brue T, Pulichino AM, Gueydan M, Barlier A, David M, Nicolino M, Malpuech G, Déchelotte P, Deal C, Van Vliet G, De Vroede M, Riepe FG, Partsch CJ, Sippell WG, Berberoglu M, Atasay B, de Zegher F, Beckers D, Kyllo J, Donohoue P, Fassnacht M, Hahner S, Allolio B, Noordam C, Dunkel L, Hero M, Pigeon B, Weill J, Yigit S, Brauner R, Heinrich JJ, Cummings E, Riddell C, Enjalbert A, Drouin J. Vallette-Kasic S, et al. Among authors: barlier a. J Clin Endocrinol Metab. 2005 Mar;90(3):1323-31. doi: 10.1210/jc.2004-1300. Epub 2004 Dec 21. J Clin Endocrinol Metab. 2005. PMID: 15613420

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