Plouin PF - Search Results

1

Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma.

Gimenez-Roqueplo AP, Favier J, Rustin P, Rieubland C, Kerlan V, Plouin PF, Rötig A, Jeunemaitre X. Gimenez-Roqueplo AP, et al. Among authors: plouin pf. J Clin Endocrinol Metab. 2002 Oct;87(10):4771-4. doi: 10.1210/jc.2002-020525. J Clin Endocrinol Metab. 2002. PMID: 12364472

2

Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.

Gimenez-Roqueplo AP, Favier J, Rustin P, Rieubland C, Crespin M, Nau V, Khau Van Kien P, Corvol P, Plouin PF, Jeunemaitre X; COMETE Network. Gimenez-Roqueplo AP, et al. Among authors: plouin pf. Cancer Res. 2003 Sep 1;63(17):5615-21. Cancer Res. 2003. PMID: 14500403

3

Year of diagnosis, features at presentation, and risk of recurrence in patients with pheochromocytoma or secreting paraganglioma.

Amar L, Servais A, Gimenez-Roqueplo AP, Zinzindohoue F, Chatellier G, Plouin PF. Amar L, et al. Among authors: plouin pf. J Clin Endocrinol Metab. 2005 Apr;90(4):2110-6. doi: 10.1210/jc.2004-1398. Epub 2005 Jan 11. J Clin Endocrinol Metab. 2005. PMID: 15644401

4

The genetic basis of pheochromocytoma: who to screen and how?

Plouin PF, Gimenez-Roqueplo AP. Plouin PF, et al. Nat Clin Pract Endocrinol Metab. 2006 Feb;2(2):60-1. doi: 10.1038/ncpendmet0097. Nat Clin Pract Endocrinol Metab. 2006. PMID: 16932255 No abstract available.

5

Initial work-up and long-term follow-up in patients with phaeochromocytomas and paragangliomas.

Plouin PF, Gimenez-Roqueplo AP. Plouin PF, et al. Best Pract Res Clin Endocrinol Metab. 2006 Sep;20(3):421-34. doi: 10.1016/j.beem.2006.07.004. Best Pract Res Clin Endocrinol Metab. 2006. PMID: 16980203 Review.

6

Phaeochromocytoma, new genes and screening strategies.

Gimenez-Roqueplo AP, Lehnert H, Mannelli M, Neumann H, Opocher G, Maher ER, Plouin PF; European Network for the Study of Adrenal Tumours (ENS@T) Pheochromocytoma Working Group. Gimenez-Roqueplo AP, et al. Among authors: plouin pf. Clin Endocrinol (Oxf). 2006 Dec;65(6):699-705. doi: 10.1111/j.1365-2265.2006.02714.x. Clin Endocrinol (Oxf). 2006. PMID: 17121518

7

Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas.

Amar L, Baudin E, Burnichon N, Peyrard S, Silvera S, Bertherat J, Bertagna X, Schlumberger M, Jeunemaitre X, Gimenez-Roqueplo AP, Plouin PF. Amar L, et al. Among authors: plouin pf. J Clin Endocrinol Metab. 2007 Oct;92(10):3822-8. doi: 10.1210/jc.2007-0709. Epub 2007 Jul 24. J Clin Endocrinol Metab. 2007. PMID: 17652212

8

[Achievements of the COMETE program in the genetics of pheochromocytoma].

Gimenez-Roqueplo AP, Burnichon N, Amar L, Favier J, Jeunemaitre X, Plouin PF. Gimenez-Roqueplo AP, et al. Among authors: plouin pf. Bull Acad Natl Med. 2008 Jan;192(1):105-15; discussion 115-6. Bull Acad Natl Med. 2008. PMID: 18663985 French.

9

The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

Burnichon N, Rohmer V, Amar L, Herman P, Leboulleux S, Darrouzet V, Niccoli P, Gaillard D, Chabrier G, Chabolle F, Coupier I, Thieblot P, Lecomte P, Bertherat J, Wion-Barbot N, Murat A, Venisse A, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP; PGL.NET network. Burnichon N, et al. Among authors: plouin pf. J Clin Endocrinol Metab. 2009 Aug;94(8):2817-27. doi: 10.1210/jc.2008-2504. Epub 2009 May 19. J Clin Endocrinol Metab. 2009. PMID: 19454582

10

A novel TMEM127 mutation in a patient with familial bilateral pheochromocytoma.

Burnichon N, Lepoutre-Lussey C, Laffaire J, Gadessaud N, Molinié V, Hernigou A, Plouin PF, Jeunemaitre X, Favier J, Gimenez-Roqueplo AP. Burnichon N, et al. Among authors: plouin pf. Eur J Endocrinol. 2011 Jan;164(1):141-5. doi: 10.1530/EJE-10-0758. Epub 2010 Oct 5. Eur J Endocrinol. 2011. PMID: 20923864

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