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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: hernigou a. 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
SFE/SFHTA/AFCE consensus on primary aldosteronism, part 4: Subtype diagnosis.
Bardet S, Chamontin B, Douillard C, Pagny JY, Hernigou A, Joffre F, Plouin PF, Steichen O. Bardet S, et al. Among authors: hernigou a. Ann Endocrinol (Paris). 2016 Jul;77(3):208-13. doi: 10.1016/j.ando.2016.01.008. Epub 2016 Mar 29. Ann Endocrinol (Paris). 2016. PMID: 27036860
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators.
Gimenez-Roqueplo AP, Caumont-Prim A, Houzard C, Hignette C, Hernigou A, Halimi P, Niccoli P, Leboulleux S, Amar L, Borson-Chazot F, Cardot-Bauters C, Delemer B, Chabolle F, Coupier I, Libé R, Peitzsch M, Peyrard S, Tenenbaum F, Plouin PF, Chatellier G, Rohmer V. Gimenez-Roqueplo AP, et al. Among authors: hernigou a. J Clin Endocrinol Metab. 2013 Jan;98(1):E162-73. doi: 10.1210/jc.2012-2975. Epub 2012 Nov 15. J Clin Endocrinol Metab. 2013. PMID: 23162105 Free article. Clinical Trial.
SFE/SFHTA/AFCE primary aldosteronism consensus: Introduction and handbook.
Amar L, Baguet JP, Bardet S, Chaffanjon P, Chamontin B, Douillard C, Durieux P, Girerd X, Gosse P, Hernigou A, Herpin D, Houillier P, Jeunemaitre X, Joffre F, Kraimps JL, Lefebvre H, Ménégaux F, Mounier-Véhier C, Nussberger J, Pagny JY, Pechère A, Plouin PF, Reznik Y, Steichen O, Tabarin A, Zennaro MC, Zinzindohoue F, Chabre O. Amar L, et al. Among authors: hernigou a. Ann Endocrinol (Paris). 2016 Jul;77(3):179-86. doi: 10.1016/j.ando.2016.05.001. Epub 2016 Jun 15. Ann Endocrinol (Paris). 2016. PMID: 27315757
100 results