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

Year Number of Results
2000 3
2001 3
2002 6
2003 5
2004 3
2005 4
2006 2
2007 4
2008 4
2009 4
2010 5
2011 1
2012 4
2013 2
2014 2
2015 5
2016 3
2017 3
2018 2
2020 4
2022 3
2023 1
2024 0

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62 results

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Page 1
Genetics of cystic fibrosis: Basics.
Férec C, Scotet V. Férec C, et al. Among authors: scotet v. Arch Pediatr. 2020 Feb;27 Suppl 1:eS4-eS7. doi: 10.1016/S0929-693X(20)30043-9. Arch Pediatr. 2020. PMID: 32172936
The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis.
Masson E, Ewers M, Paliwal S, Kume K, Scotet V, Cooper DN, Rebours V, Buscail L, Rouault K; GREPAN (Genetic REsearch on PANcreatitis) Study Group; Abrantes A, Aguilera Munoz L, Albouys J, Alric L, Amiot X, Archambeaud I, Audiau S, Bastide L, Baudon J, Bellaiche G, Bellon S, Bertrand V, Bideau K, Billiemaz K, Billioud C, Bonnefoy S, Borderon C, Bournet B, Breton E, Brugel M, Buscail L, Cadiot G, Camus M, Carpentier-Pourquier M, Chamouard P, Chaput U, Chen JM, Cholet F, Ciocan DM, Clavel C, Coffin B, Coimet-Berger L, Cosconea S, Creveaux I, Culetto A, Daboussi O, De Mestier L, Degand T, D'engremont C, Denis B, Dermine S, Desgrippes, Drouet D'Aubigny A, Enaud R, Fabre A, Férec C, Gargot D, Gelsi E, Gentilcore E, Gincul R, Ginglinger-Favre E, Giovannini M, Gomercic C, Gondran H, Grainville T, Grandval P, Grasset D, Grimaldi S, Grimbert S, Hagege H, Heissat S, Hentic O, Herber-Mayne A, Hervouet M, Hoibian S, Jacques J, Jais B, Kaassis M, Koch S, Lacaze E, Lacroute J, Lamireau T, Laurent L, Le Guillou X, Le Rhun M, Leblanc S, Levy P, Lievre A, Lorenzo D, Maire F, Marcel K, Masson E, Mauillon J, Morgant S, Moussata D, Muller N, Nambot S, Napoleon B, Olivier A, Pagenault M, Pelleti… See abstract for full author list ➔ Masson E, et al. Among authors: scotet v. Pancreatology. 2023 Jan;23(1):48-56. doi: 10.1016/j.pan.2022.11.013. Epub 2022 Dec 5. Pancreatology. 2023. PMID: 36517351
[Neonatal screening for cystic fibrosis].
Scotet V, Audrézet MP, de Braekeleer M, Férec C. Scotet V, et al. Pathol Biol (Paris). 2001 Dec;49(10):785-8. doi: 10.1016/s0369-8114(01)00245-0. Pathol Biol (Paris). 2001. PMID: 11776687 French. No abstract available.
Primary sclerosing cholangitis is associated with abnormalities in CFTR.
Werlin S, Scotet V, Uguen K, Audrezet MP, Cohen M, Yaakov Y, Safadi R, Ilan Y, Konikoff F, Galun E, Mizrahi M, Slae M, Sayag S, Cohen-Cymberknoh M, Wilschanski M, Ferec C. Werlin S, et al. Among authors: scotet v. J Cyst Fibros. 2018 Sep;17(5):666-671. doi: 10.1016/j.jcf.2018.04.005. Epub 2018 May 26. J Cyst Fibros. 2018. PMID: 29807875 Free article.
[Genetics and modifier genes, atypical and rare forms].
Férec C, Scotet V, Beucher J, Corvol H. Férec C, et al. Among authors: scotet v. Arch Pediatr. 2012 May;19 Suppl 1:S3-7. doi: 10.1016/S0929-693X(12)71099-0. Arch Pediatr. 2012. PMID: 22682487 Review. French.
Prevalence of HFE-related haemochromatosis and secondary causes of hyperferritinaemia and their association with iron overload in 1059 French patients treated by venesection.
Le Gac G, Scotet V, Gourlaouen I, L'Hostis C, Merour MC, Karim Z, Deugnier Y, Bardou-Jacquet E, Lefebvre T, Assari S, Ferec C. Le Gac G, et al. Among authors: scotet v. Aliment Pharmacol Ther. 2022 Apr;55(8):1016-1027. doi: 10.1111/apt.16775. Epub 2022 Feb 4. Aliment Pharmacol Ther. 2022. PMID: 35122291
62 results