Pigny P - Search Results

1

Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma.

Ben Aim L, Pigny P, Castro-Vega LJ, Buffet A, Amar L, Bertherat J, Drui D, Guilhem I, Baudin E, Lussey-Lepoutre C, Corsini C, Chabrier G, Briet C, Faivre L, Cardot-Bauters C, Favier J, Gimenez-Roqueplo AP, Burnichon N. Ben Aim L, et al. Among authors: pigny p. J Med Genet. 2019 Aug;56(8):513-520. doi: 10.1136/jmedgenet-2018-105714. Epub 2019 Mar 15. J Med Genet. 2019. PMID: 30877234

2

Changes in circulating forms of anti-Muüllerian hormone and androgens in women with and without PCOS: a systematic longitudinal study throughout pregnancy.

Peigné M, Simon V, Pigny P, Mimouni NEH, Martin C, Dewailly D, Catteau-Jonard S, Giacobini P. Peigné M, et al. Among authors: pigny p. Hum Reprod. 2023 May 2;38(5):938-950. doi: 10.1093/humrep/dead050. Hum Reprod. 2023. PMID: 36921289 Free PMC article.

3

Contribution of genetic analysis in screening for MEN1 among patients with sporadic disease and one or more typical manifestation.

Odou MF, Cardot-Bauters C, Vantyghem MC, Carnaille B, Leteurtre E, Pigny P, Verier-Mine O, Desailloud R, Porchet N. Odou MF, et al. Among authors: pigny p. Ann Endocrinol (Paris). 2006 Dec;67(6):581-7. doi: 10.1016/s0003-4266(06)73010-4. Ann Endocrinol (Paris). 2006. PMID: 17194968

4

Paraganglioma after maternal transmission of a succinate dehydrogenase gene mutation.

Pigny P, Vincent A, Cardot Bauters C, Bertrand M, de Montpreville VT, Crepin M, Porchet N, Caron P. Pigny P, et al. J Clin Endocrinol Metab. 2008 May;93(5):1609-15. doi: 10.1210/jc.2007-1989. Epub 2008 Jan 22. J Clin Endocrinol Metab. 2008. PMID: 18211978

5

Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?

Cardot-Bauters C, Leteurtre E, Leclerc L, Vantyghem MC, Do Cao C, Wemeau JL, d'Herbomez M, Carnaille B, Barbu V, Pinson S, Pigny P; Groupe d'Etude des Tumeurs Endocrines (GTE). Cardot-Bauters C, et al. Among authors: pigny p. Clin Endocrinol (Oxf). 2008 Sep;69(3):506-10. doi: 10.1111/j.1365-2265.2008.03230.x. Epub 2008 Mar 10. Clin Endocrinol (Oxf). 2008. PMID: 18331611

6

A germline mutation of the KIF1B beta gene on 1p36 in a family with neural and nonneural tumors.

Yeh IT, Lenci RE, Qin Y, Buddavarapu K, Ligon AH, Leteurtre E, Do Cao C, Cardot-Bauters C, Pigny P, Dahia PL. Yeh IT, et al. Among authors: pigny p. Hum Genet. 2008 Oct;124(3):279-85. doi: 10.1007/s00439-008-0553-1. Epub 2008 Aug 26. Hum Genet. 2008. PMID: 18726616

7

Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?

Pigny P, Cardot-Bauters C, Do Cao C, Vantyghem MC, Carnaille B, Pattou F, Caron P, Wemeau JL, Porchet N. Pigny P, et al. Eur J Endocrinol. 2009 Feb;160(2):227-31. doi: 10.1530/EJE-08-0574. Epub 2008 Nov 24. Eur J Endocrinol. 2009. PMID: 19029228

8

Local-regional recurrence of sporadic or syndromic abdominal extra-adrenal paraganglioma: incidence, characteristics, and outcome.

Van Slycke S, Caiazzo R, Pigny P, Cardot-Bauters C, Arnalsteen L, D'Herbomez M, Leteurtre E, Rouaix-Emery N, Ernst O, Huglo D, Vantyghem MC, Wemeau JL, Carnaille B, Pattou F. Van Slycke S, et al. Among authors: pigny p. Surgery. 2009 Dec;146(6):986-92. doi: 10.1016/j.surg.2009.10.055. Surgery. 2009. PMID: 19958924

9

Genetics of pheochromocytoma and paraganglioma: new developments.

Pigny P, Cardot-Bauters C. Pigny P, et al. Ann Endocrinol (Paris). 2010 Mar;71(2):76-82. doi: 10.1016/j.ando.2009.11.004. Epub 2009 Dec 22. Ann Endocrinol (Paris). 2010. PMID: 20031114 Review.

10

VHL mosaicism can be detected by clinical next-generation sequencing and is not restricted to patients with a mild phenotype.

Coppin L, Grutzmacher C, Crépin M, Destailleur E, Giraud S, Cardot-Bauters C, Porchet N, Pigny P. Coppin L, et al. Among authors: pigny p. Eur J Hum Genet. 2014 Sep;22(9):1149-52. doi: 10.1038/ejhg.2013.279. Epub 2013 Dec 4. Eur J Hum Genet. 2014. PMID: 24301059 Free PMC article.

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