Amselem S - Search Results

1

Atypical presentation of a cryopyrin-associated periodic syndrome, revealing a novel NLRP3 mutation.

Canouï E, Maigné G, Jéru I, Amselem S, Koné-Paut I, Lambotte O. Canouï E, et al. Among authors: amselem s. Clin Immunol. 2013 Aug;148(2):299-300. doi: 10.1016/j.clim.2013.05.020. Epub 2013 Jun 12. Clin Immunol. 2013. PMID: 23811320 Free article. No abstract available.

2

[Inflammasome and interleukin 1].

Jéru I, Amselem S. Jéru I, et al. Among authors: amselem s. Rev Med Interne. 2011 Apr;32(4):218-24. doi: 10.1016/j.revmed.2010.02.013. Epub 2010 Jun 11. Rev Med Interne. 2011. PMID: 20541850 French.

3

Mutations in the autoinflammatory cryopyrin-associated periodic syndrome gene: epidemiological study and lessons from eight years of genetic analysis in France.

Cuisset L, Jeru I, Dumont B, Fabre A, Cochet E, Le Bozec J, Delpech M, Amselem S, Touitou I; French CAPS study group. Cuisset L, et al. Among authors: amselem s. Ann Rheum Dis. 2011 Mar;70(3):495-9. doi: 10.1136/ard.2010.138420. Epub 2010 Nov 24. Ann Rheum Dis. 2011. PMID: 21109514

4

PYPAF1 nonsense mutation in a patient with an unusual autoinflammatory syndrome: role of PYPAF1 in inflammation.

Jéru I, Hayrapetyan H, Duquesnoy P, Sarkisian T, Amselem S. Jéru I, et al. Among authors: amselem s. Arthritis Rheum. 2006 Feb;54(2):508-14. doi: 10.1002/art.21618. Arthritis Rheum. 2006. PMID: 16447225 Free article.

5

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: amselem s. Arthritis Rheum. 2010 Apr;62(4):1176-85. doi: 10.1002/art.27326. Arthritis Rheum. 2010. PMID: 20131254 Free article.

6

Familial Mediterranean fever in heterozygotes: are we able to accurately diagnose the disease in very young children?

Hentgen V, Grateau G, Stankovic-Stojanovic K, Amselem S, Jéru I. Hentgen V, et al. Among authors: amselem s. Arthritis Rheum. 2013 Jun;65(6):1654-62. doi: 10.1002/art.37935. Arthritis Rheum. 2013. PMID: 23508419 Free article.

7

[Molecular bases of hereditary recurrent fevers].

Jéru I, Grateau G, Amselem S. Jéru I, et al. Among authors: amselem s. Pathol Biol (Paris). 2009 May;57(3):213-6. doi: 10.1016/j.patbio.2008.04.008. Epub 2008 Jun 13. Pathol Biol (Paris). 2009. PMID: 18554823 French. No abstract available.

8

Subcellular localisation of marenostrin/pyrin isoforms carrying the most common mutations involved in familial Mediterranean fever in the presence or absence of its binding partner ASC.

Cazeneuve C, Papin S, Jéru I, Duquesnoy P, Amselem S. Cazeneuve C, et al. Among authors: amselem s. J Med Genet. 2004 Mar;41(3):e24. doi: 10.1136/jmg.2003.011601. J Med Genet. 2004. PMID: 14985395 Free PMC article. No abstract available.

9

The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approach.

Jéru I, Hentgen V, Cochet E, Duquesnoy P, Le Borgne G, Grimprel E, Stojanovic KS, Karabina S, Grateau G, Amselem S. Jéru I, et al. Among authors: amselem s. PLoS One. 2013 Jul 3;8(7):e68431. doi: 10.1371/journal.pone.0068431. Print 2013. PLoS One. 2013. PMID: 23844200 Free PMC article.

10

Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes.

Jéru I, Le Borgne G, Cochet E, Hayrapetyan H, Duquesnoy P, Grateau G, Morali A, Sarkisian T, Amselem S. Jéru I, et al. Among authors: amselem s. Arthritis Rheum. 2011 May;63(5):1459-64. doi: 10.1002/art.30241. Arthritis Rheum. 2011. PMID: 21538323 Free article.

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