Vallette-Kasic S - Search Results

1

Macroprolactinemia revisited: a study on 106 patients.

Vallette-Kasic S, Morange-Ramos I, Selim A, Gunz G, Morange S, Enjalbert A, Martin PM, Jaquet P, Brue T. Vallette-Kasic S, et al. J Clin Endocrinol Metab. 2002 Feb;87(2):581-8. doi: 10.1210/jcem.87.2.8272. J Clin Endocrinol Metab. 2002. PMID: 11836289

2

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. J Clin Endocrinol Metab. 2001 Sep;86(9):4529-35. doi: 10.1210/jcem.86.9.7811. J Clin Endocrinol Metab. 2001. PMID: 11549703

3

Differential regulation of proopiomelanocortin and pituitary-restricted transcription factor (TPIT), a new marker of normal and adenomatous human corticotrophs.

Vallette-Kasic S, Figarella-Branger D, Grino M, Pulichino AM, Dufour H, Grisoli F, Enjalbert A, Drouin J, Brue T. Vallette-Kasic S, et al. J Clin Endocrinol Metab. 2003 Jul;88(7):3050-6. doi: 10.1210/jc.2002-021934. J Clin Endocrinol Metab. 2003. PMID: 12843142

4

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

5

The desmopressin test as a predictive factor of outcome after pituitary surgery for Cushing's disease.

Valéro R, Vallette-Kasic S, Conte-Devolx B, Jaquet P, Brue T. Valéro R, et al. Eur J Endocrinol. 2004 Dec;151(6):727-33. doi: 10.1530/eje.0.1510727. Eur J Endocrinol. 2004. PMID: 15588239 Clinical Trial.

6

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: vallette kasic s. 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

7

Markers of tumor invasion are major predictive factors for the long-term outcome of corticotroph microadenomas treated by transsphenoidal adenomectomy.

Vallette-Kasic S, Dufour H, Mugnier M, Trouillas J, Valdes-Socin H, Caron P, Morange S, Girard N, Grisoli F, Jaquet P, Brue T. Vallette-Kasic S, et al. Eur J Endocrinol. 2000 Dec;143(6):761-8. doi: 10.1530/eje.0.1430761. Eur J Endocrinol. 2000. PMID: 11124859

8

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: vallette kasic s. 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

9

Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: functional and structural correlates.

Vallette-Kasic S, Pellegrini-Bouiller I, Sampieri F, Gunz G, Diaz A, Radovick S, Enjalbert A, Brue T. Vallette-Kasic S, et al. Mol Endocrinol. 2001 Mar;15(3):411-20. doi: 10.1210/mend.15.3.0601. Mol Endocrinol. 2001. PMID: 11222742

10

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: vallette kasic s. 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

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