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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
2003 1
2004 1
2005 1
2006 1
2008 1
2009 2
2010 3
2011 6
2012 1
2013 3
2014 4
2015 2
2016 1
2018 2
2019 1
2023 1
2024 0

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29 results

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Page 1
Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation.
Masters SL, Lagou V, Jéru I, Baker PJ, Van Eyck L, Parry DA, Lawless D, De Nardo D, Garcia-Perez JE, Dagley LF, Holley CL, Dooley J, Moghaddas F, Pasciuto E, Jeandel PY, Sciot R, Lyras D, Webb AI, Nicholson SE, De Somer L, van Nieuwenhove E, Ruuth-Praz J, Copin B, Cochet E, Medlej-Hashim M, Megarbane A, Schroder K, Savic S, Goris A, Amselem S, Wouters C, Liston A. Masters SL, et al. Among authors: cochet e. Sci Transl Med. 2016 Mar 30;8(332):332ra45. doi: 10.1126/scitranslmed.aaf1471. Sci Transl Med. 2016. PMID: 27030597 Free article.
Bilateral cochlear implantation in children.
Vermeire K, Brokx JP, Van de Heyning PH, Cochet E, Carpentier H. Vermeire K, et al. Among authors: cochet e. Int J Pediatr Otorhinolaryngol. 2003 Jan;67(1):67-70. doi: 10.1016/s0165-5876(02)00286-0. Int J Pediatr Otorhinolaryngol. 2003. PMID: 12560152
Molecular architecture and function of the SEA complex, a modulator of the TORC1 pathway.
Algret R, Fernandez-Martinez J, Shi Y, Kim SJ, Pellarin R, Cimermancic P, Cochet E, Sali A, Chait BT, Rout MP, Dokudovskaya S. Algret R, et al. Among authors: cochet e. Mol Cell Proteomics. 2014 Nov;13(11):2855-70. doi: 10.1074/mcp.M114.039388. Epub 2014 Jul 29. Mol Cell Proteomics. 2014. PMID: 25073740 Free PMC article.
Brief Report: Involvement of TNFRSF11A molecular defects in autoinflammatory disorders.
Jéru I, Cochet E, Duquesnoy P, Hentgen V, Copin B, Mitjavila-Garcia MT, Sheykholeslami S, Le Borgne G, Dastot-Le Moal F, Malan V, Karabina S, Mahevas M, Chantot-Bastaraud S, Lecron JC, Faivre L, Amselem S. Jéru I, et al. Among authors: cochet e. Arthritis Rheumatol. 2014 Sep;66(9):2621-7. doi: 10.1002/art.38727. Arthritis Rheumatol. 2014. PMID: 24891336
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies.
Valence S, Cochet E, Rougeot C, Garel C, Chantot-Bastaraud S, Lainey E, Afenjar A, Barthez MA, Bednarek N, Doummar D, Faivre L, Goizet C, Haye D, Heron B, Kemlin I, Lacombe D, Milh M, Moutard ML, Riant F, Robin S, Roubertie A, Sarda P, Toutain A, Villard L, Ville D, Billette de Villemeur T, Rodriguez D, Burglen L. Valence S, et al. Among authors: cochet e. Genet Med. 2019 Mar;21(3):553-563. doi: 10.1038/s41436-018-0089-2. Epub 2018 Jul 12. Genet Med. 2019. PMID: 29997391 Free article.
29 results