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[Familial Mediterranean fever].
Georgin-Lavialle S, Hentgen V, Stankovic Stojanovic K, Bachmeyer C, Rodrigues F, Savey L, Abbara S, Conan PL, Fraisse T, Delplanque M, Rouet A, Sbeih N, Koné-Paut I, Grateau G. Georgin-Lavialle S, et al. Among authors: hentgen v. Rev Med Interne. 2018 Apr;39(4):240-255. doi: 10.1016/j.revmed.2018.02.005. Epub 2018 Mar 8. Rev Med Interne. 2018. PMID: 29526329 French.
[Hereditary intermittant fever].
Grateau G, Granel B, Hentgen V, Dodé C, Cuisset L, Delpech M. Grateau G, et al. Among authors: hentgen v. Presse Med. 2004 Oct 9;33(17):1195-206. doi: 10.1016/s0755-4982(04)98889-6. Presse Med. 2004. PMID: 15523291 Review. French.
[The child with fever in pyrins time].
Koné-Paut I, Hentgen V, Guillaume S, Touitou I. Koné-Paut I, et al. Among authors: hentgen v. Arch Pediatr. 2007 Jun;14(6):652-5. doi: 10.1016/j.arcped.2007.04.003. Epub 2007 Apr 24. Arch Pediatr. 2007. PMID: 17459676 French. No abstract available.
Mutations in NALP12 cause hereditary periodic fever syndromes.
Jéru I, Duquesnoy P, Fernandes-Alnemri T, Cochet E, Yu JW, Lackmy-Port-Lis M, Grimprel E, Landman-Parker J, Hentgen V, Marlin S, McElreavey K, Sarkisian T, Grateau G, Alnemri ES, Amselem S. Jéru I, et al. Among authors: hentgen v. Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1614-9. doi: 10.1073/pnas.0708616105. Epub 2008 Jan 29. Proc Natl Acad Sci U S A. 2008. PMID: 18230725 Free PMC article.
[Auto-inflammatory syndromes and pregnancy].
Stankovic K, Hentgen V, Grateau G. Stankovic K, et al. Among authors: hentgen v. Presse Med. 2008 Nov;37(11):1676-82. doi: 10.1016/j.lpm.2008.08.002. Epub 2008 Sep 24. Presse Med. 2008. PMID: 18818048 Review. French.
The clinical spectrum of 94 patients carrying a single mutated MEFV allele.
Koné-Paut I, Hentgen V, Guillaume-Czitrom S, Compeyrot-Lacassagne S, Tran TA, Touitou I. Koné-Paut I, et al. Among authors: hentgen v. Rheumatology (Oxford). 2009 Jul;48(7):840-2. doi: 10.1093/rheumatology/kep121. Epub 2009 May 22. Rheumatology (Oxford). 2009. PMID: 19465590
Functional consequences of a germline mutation in the leucine-rich repeat domain of NLRP3 identified in an atypical autoinflammatory disorder.
Jéru I, Marlin S, Le Borgne G, Cochet E, Normand S, Duquesnoy P, Dastot-Le Moal F, Cuisset L, Hentgen V, Fernandes Alnemri T, Lecron JC, Dhote R, Grateau G, Alnemri ES, Amselem S. Jéru I, et al. Among authors: hentgen v. Arthritis Rheum. 2010 Apr;62(4):1176-85. doi: 10.1002/art.27326. Arthritis Rheum. 2010. PMID: 20131254 Free article.
148 results