Brue T - Search Results

1

Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations.

Castets S, Roucher-Boulez F, Saveanu A, Mallet-Motak D, Chabre O, Amati-Bonneau P, Bonneau D, Girardin C, Morel Y, Villanueva C, Brue T, Reynaud R, Nicolino M. Castets S, et al. Among authors: brue t. Horm Res Paediatr. 2020;93(1):30-39. doi: 10.1159/000507249. Epub 2020 May 26. Horm Res Paediatr. 2020. PMID: 32454486

2

[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: brue t. Presse Med. 2004 Mar 27;33(6):400-5. doi: 10.1016/s0755-4982(04)98607-1. Presse Med. 2004. PMID: 15105786 Review. French.

3

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: brue t. J Clin Endocrinol Metab. 2004 Nov;89(11):5779-86. doi: 10.1210/jc.2003-032124. J Clin Endocrinol Metab. 2004. PMID: 15531542

4

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: brue t. 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

5

Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.

Turton JP, Reynaud R, Mehta A, Torpiano J, Saveanu A, Woods KS, Tiulpakov A, Zdravkovic V, Hamilton J, Attard-Montalto S, Parascandalo R, Vella C, Clayton PE, Shalet S, Barton J, Brue T, Dattani MT. Turton JP, et al. Among authors: brue t. J Clin Endocrinol Metab. 2005 Aug;90(8):4762-70. doi: 10.1210/jc.2005-0570. Epub 2005 May 31. J Clin Endocrinol Metab. 2005. PMID: 15928241

6

An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domain.

Reynaud R, Barlier A, Vallette-Kasic S, Saveanu A, Guillet MP, Simonin G, Enjalbert A, Valensi P, Brue T. Reynaud R, et al. Among authors: brue t. J Clin Endocrinol Metab. 2005 Aug;90(8):4880-7. doi: 10.1210/jc.2005-0119. Epub 2005 Jun 7. J Clin Endocrinol Metab. 2005. PMID: 15941866

7

Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.

Reynaud R, Gueydan M, Saveanu A, Vallette-Kasic S, Enjalbert A, Brue T, Barlier A. Reynaud R, et al. Among authors: brue t. J Clin Endocrinol Metab. 2006 Sep;91(9):3329-36. doi: 10.1210/jc.2005-2173. Epub 2006 May 30. J Clin Endocrinol Metab. 2006. PMID: 16735499

8

Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.

Miyata I, Vallette-Kasic S, Saveanu A, Takeuchi M, Yoshikawa H, Tajima A, Tojo K, Reynaud R, Gueydan M, Enjalbert A, Tajima N, Eto Y, Brue T. Miyata I, et al. Among authors: brue t. J Clin Endocrinol Metab. 2006 Dec;91(12):4981-7. doi: 10.1210/jc.2005-2289. Epub 2006 Sep 12. J Clin Endocrinol Metab. 2006. PMID: 16968807

9

Somatostatin receptor sst2 decreases cell viability and hormonal hypersecretion and reverses octreotide resistance of human pituitary adenomas.

Acunzo J, Thirion S, Roche C, Saveanu A, Gunz G, Germanetti AL, Couderc B, Cohen R, Figarella-Branger D, Dufour H, Brue T, Enjalbert A, Barlier A. Acunzo J, et al. Among authors: brue t. Cancer Res. 2008 Dec 15;68(24):10163-70. doi: 10.1158/0008-5472.CAN-08-1857. Cancer Res. 2008. PMID: 19074883

10

Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency.

Nyström HF, Saveanu A, Barbosa EJ, Barlier A, Enjalbert A, Glad C, Palming J, Johannsson G, Brue T. Nyström HF, et al. Among authors: brue t. Pituitary. 2011 Sep;14(3):208-16. doi: 10.1007/s11102-010-0278-8. Pituitary. 2011. PMID: 21132537

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

331 results

Search Page