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

Year Number of Results
2001 1
2003 1
2004 9
2005 5
2006 4
2007 6
2008 6
2009 2
2011 1
2015 2
2016 4
2019 2
2020 2
2022 1
2023 1
2024 1

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45 results

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Page 1
[Imaging of complications of Meckel diverticulum].
Barbary C, Tissier S, Floquet M, Régent D. Barbary C, et al. Among authors: tissier s. J Radiol. 2004 Mar;85(3):273-9. doi: 10.1016/s0221-0363(04)97578-6. J Radiol. 2004. PMID: 15192518 Review. French.
[Cardiac imaging].
Sablayrolles JL, Jacquier A, Tissier S. Sablayrolles JL, et al. Among authors: tissier s. J Radiol. 2004 Jul-Aug;85(7-8):979-85. doi: 10.1016/s0221-0363(04)97708-6. J Radiol. 2004. PMID: 15331997 French. No abstract available.
[Vascular and interventional radiology].
Sablayrolles JL, Jacquier A, Tissier S. Sablayrolles JL, et al. Among authors: tissier s. J Radiol. 2004 Jul-Aug;85(7-8):986-7. doi: 10.1016/s0221-0363(04)97709-8. J Radiol. 2004. PMID: 15331998 French. No abstract available.
Primary ciliary dyskinesia gene contribution in Tunisia: Identification of a major Mediterranean allele.
Mani R, Belkacem S, Soua Z, Chantot S, Montantin G, Tissier S, Copin B, Bouguila J, Rive Le Gouard N, Boughamoura L, Ben Ameur S, Hachicha M, Boussoffara R, Boussetta K, Hammouda S, Bedoui A, Besbes H, Meddeb S, Chraeit K, Khlifa M, Escudier E, Amselem S, Mabrouk I, Legendre M. Mani R, et al. Among authors: tissier s. Hum Mutat. 2020 Jan;41(1):115-121. doi: 10.1002/humu.23905. Epub 2019 Sep 15. Hum Mutat. 2020. PMID: 31469207
Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients.
Mabrouk I, Al-Harthi N, Mani R, Montantin G, Tissier S, Lagha R, Ben Abdallah F, Hassan MM, Alhomrani M, Gaber A, Alsanie WF, Ouali H, Jambi FA, Almaghamsi TM, Alqarni NA, Alfarsi NA, Kashgari K, Al-Zahrani HJ, Al-Shamary ZA, Al-Harbi A, Amselem S, Escudier E, Legendre M. Mabrouk I, et al. Among authors: tissier s. J Hum Genet. 2022 Jul;67(7):381-386. doi: 10.1038/s10038-021-01006-9. Epub 2022 Jan 20. J Hum Genet. 2022. PMID: 35046476
Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer.
Nathan N, Giraud V, Picard C, Nunes H, Dastot-Le Moal F, Copin B, Galeron L, De Ligniville A, Kuziner N, Reynaud-Gaubert M, Valeyre D, Couderc LJ, Chinet T, Borie R, Crestani B, Simansour M, Nau V, Tissier S, Duquesnoy P, Mansour-Hendili L, Legendre M, Kannengiesser C, Coulomb-L'Hermine A, Gouya L, Amselem S, Clement A. Nathan N, et al. Among authors: tissier s. Hum Mol Genet. 2016 Apr 15;25(8):1457-67. doi: 10.1093/hmg/ddw014. Epub 2016 Jan 19. Hum Mol Genet. 2016. PMID: 26792177
[Mucocele of the appendix and pseudomyxoma peritonei].
Fairise A, Barbary C, Derelle A, Tissier S, Granger P, Marchal F, Laurent V, Régent D. Fairise A, et al. Among authors: tissier s. J Radiol. 2008 Jun;89(6):751-62. doi: 10.1016/s0221-0363(08)73781-8. J Radiol. 2008. PMID: 18641562 French. No abstract available.
45 results