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287 results

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Page 1
Lessons from prospective longitudinal follow-up of a French APECED cohort.
Humbert L, Proust-Lemoine E, Dubucquoi S, Kemp EH, Saugier-Veber P, Fabien N, Raymond-Top I, Cardot-Bauters C, Carel JC, Cartigny M, Chabre O, Chanson P, Delemer B, Do Cao C, Guignat L, Kahn JE, Kerlan V, Lefebvre H, Linglart A, Mallone R, Reynaud R, Sendid B, Souchon PF, Touraine P, Wémeau JL, Vantyghem MC. Humbert L, et al. Among authors: vantyghem mc. J Clin Endocrinol Metab. 2024 Apr 12:dgae211. doi: 10.1210/clinem/dgae211. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38605470 Free article.
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.
Giraud S, Zhang CX, Serova-Sinilnikova O, Wautot V, Salandre J, Buisson N, Waterlot C, Bauters C, Porchet N, Aubert JP, Emy P, Cadiot G, Delemer B, Chabre O, Niccoli P, Leprat F, Duron F, Emperauger B, Cougard P, Goudet P, Sarfati E, Riou JP, Guichard S, Rodier M, Meyrier A, Caron P, Vantyghem MC, Assayag M, Peix JL, Pugeat M, Rohmer V, Vallotton M, Lenoir G, Gaudray P, Proye C, Conte-Devolx B, Chanson P, Shugart YY, Goldgar D, Murat A, Calender A. Giraud S, et al. Among authors: vantyghem mc. Am J Hum Genet. 1998 Aug;63(2):455-67. doi: 10.1086/301953. Am J Hum Genet. 1998. PMID: 9683585 Free PMC article.
[Pseudo-hypoaldosteronisms].
Vantyghem MC, Perimenis P, Wemeau JL. Vantyghem MC, et al. Presse Med. 2004 Jan 31;33(2):123-9. doi: 10.1016/s0755-4982(04)98501-6. Presse Med. 2004. PMID: 15026708 Review. French.
[Congenital hypomagnesemia].
Montaigne D, Perimenis P, Douillard C, Wemeau JL, Vantyghem MC. Montaigne D, et al. Among authors: vantyghem mc. Presse Med. 2004 Nov 6;33(19 Pt 1):1341-8. doi: 10.1016/s0755-4982(04)98921-x. Presse Med. 2004. PMID: 15615242 Review. French.
A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.
Groussin L, Horvath A, Jullian E, Boikos S, Rene-Corail F, Lefebvre H, Cephise-Velayoudom FL, Vantyghem MC, Chanson P, Conte-Devolx B, Lucas M, Gentil A, Malchoff CD, Tissier F, Carney JA, Bertagna X, Stratakis CA, Bertherat J. Groussin L, et al. Among authors: vantyghem mc. J Clin Endocrinol Metab. 2006 May;91(5):1943-9. doi: 10.1210/jc.2005-2708. Epub 2006 Feb 7. J Clin Endocrinol Metab. 2006. PMID: 16464939 Free article.
New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome.
Decaudain A, Vantyghem MC, Guerci B, Hécart AC, Auclair M, Reznik Y, Narbonne H, Ducluzeau PH, Donadille B, Lebbé C, Béréziat V, Capeau J, Lascols O, Vigouroux C. Decaudain A, et al. Among authors: vantyghem mc. J Clin Endocrinol Metab. 2007 Dec;92(12):4835-44. doi: 10.1210/jc.2007-0654. Epub 2007 Aug 21. J Clin Endocrinol Metab. 2007. PMID: 17711925
[Riedel's thyroiditis: current aspects].
Perimenis P, Marcelli S, Leteurtre E, Vantyghem MC, Wémeau JL. Perimenis P, et al. Among authors: vantyghem mc. Presse Med. 2008 Jun;37(6 Pt 2):1015-21. doi: 10.1016/j.lpm.2007.07.021. Epub 2007 Dec 21. Presse Med. 2008. PMID: 18160252 Review. French.
287 results