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

Year Number of Results
1995 1
2000 1
2001 3
2003 2
2004 2
2009 1
2010 2
2011 1
2014 1
2015 1
2016 1
2017 1
2018 1
2019 2
2021 0
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19 results
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Page 1
Role of sodium in dialysis.
Charra B, Chazot C, Jean G, Hurot JM, Terrat JC, Vanel T, Lorriaux C, Vovan C. Charra B, et al. Among authors: vovan c. Minerva Urol Nefrol. 2004 Sep;56(3):205-13. Minerva Urol Nefrol. 2004. PMID: 15467499 Free article. Review.
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy.
Nguyen K, Puppo F, Roche S, Gaillard MC, Chaix C, Lagarde A, Pierret M, Vovan C, Olschwang S, Salort-Campana E, Attarian S, Bartoli M, Bernard R, Magdinier F, Levy N. Nguyen K, et al. Among authors: vovan c. Hum Mutat. 2017 Oct;38(10):1432-1441. doi: 10.1002/humu.23304. Epub 2017 Aug 6. Hum Mutat. 2017. PMID: 28744936 Free article.
Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism.
Roche S, Dion C, Broucqsault N, Laberthonnière C, Gaillard MC, Robin JD, Lagarde A, Puppo F, Vovan C, Chaix C, Campana ES, Attarian S, Bartoli M, Bernard R, Nguyen K, Magdinier F. Roche S, et al. Among authors: vovan c. Neurol Genet. 2019 Nov 14;5(6):e372. doi: 10.1212/NXG.0000000000000372. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 31872053 Free PMC article.
Comparison of survival data.
Charra B, Hurot JM, Chazot C, VoVan C, Jean G, Terrat JC, Vanel T, Ruffet M, Laurent G. Charra B, et al. Among authors: vovan c. Kidney Int. 2000 Aug;58(2):901-2. doi: 10.1046/j.1523-1755.2000.00244.x. Kidney Int. 2000. PMID: 10916119 Free article. No abstract available.
Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome.
Renard D, Taieb G, Garibaldi M, Maues De Paula A, Bernard R, Lagha N, Cristofari G, Vovan C, Chaix C, Lévy N, Khau Van Kien P, Sacconi S. Renard D, et al. Among authors: vovan c. Am J Med Genet A. 2018 Aug;176(8):1760-1763. doi: 10.1002/ajmg.a.38843. Epub 2018 Jul 28. Am J Med Genet A. 2018. PMID: 30055030
Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy.
Nguyen K, Broucqsault N, Chaix C, Roche S, Robin JD, Vovan C, Gerard L, Mégarbané A, Urtizberea JA, Bellance R, Barnérias C, David A, Eymard B, Fradin M, Manel V, Sacconi S, Tiffreau V, Zagnoli F, Cuisset JM, Salort-Campana E, Attarian S, Bernard R, Lévy N, Magdinier F. Nguyen K, et al. Among authors: vovan c. J Med Genet. 2019 Sep;56(9):590-601. doi: 10.1136/jmedgenet-2018-105949. Epub 2019 Apr 22. J Med Genet. 2019. PMID: 31010831
Malnutrition in long-term haemodialysis survivors.
Chazot C, Laurent G, Charra B, Blanc C, VoVan C, Jean G, Vanel T, Terrat JC, Ruffet M. Chazot C, et al. Among authors: vovan c. Nephrol Dial Transplant. 2001 Jan;16(1):61-9. doi: 10.1093/ndt/16.1.61. Nephrol Dial Transplant. 2001. PMID: 11208995
Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers.
Gaillard MC, Roche S, Dion C, Tasmadjian A, Bouget G, Salort-Campana E, Vovan C, Chaix C, Broucqsault N, Morere J, Puppo F, Bartoli M, Levy N, Bernard R, Attarian S, Nguyen K, Magdinier F. Gaillard MC, et al. Among authors: vovan c. Neurology. 2014 Aug 19;83(8):733-42. doi: 10.1212/WNL.0000000000000708. Epub 2014 Jul 16. Neurology. 2014. PMID: 25031281
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