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

Year Number of Results
1990 1
1991 2
1992 2
1993 1
1995 1
1998 1
2000 1
2001 1
2004 2
2005 2
2006 3
2007 1
2008 1
2009 2
2010 2
2011 1
2012 2
2013 1
2014 1
2017 1
2019 1
2021 1
2024 0

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27 results

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Page 1
[Indications of electroencephalogram in the newborn].
Lamblin MD, André M, Auzoux M, Bednarek N, Bour F, Charollais A, Cheliout-Heraut F, D'Allest AM, De Bellecize J, Delanoe C, Furby A, Frenkel AL, Keo-Kosal P, Mony L, Moutard ML, Navelet Y, Nedelcoux H, Nguyen TT, Nogues B, Plouin P, Salefranque F, Soufflet C, Touzery de Villepin A, Vecchierini MF, Wallois F, Esquivel-Walls E. Lamblin MD, et al. Among authors: furby a. Arch Pediatr. 2004 Jul;11(7):829-33. doi: 10.1016/j.arcped.2004.01.031. Arch Pediatr. 2004. PMID: 15234381 Review. French.
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?].
Meininger V, Antoine JC, Arne-Bes MC, Broussolle E, Bruneteau G, Camdessanche JP, Camu W, Carluer L, Cintas P, Clavelou P, Corcia P, Couratier P, Danel-Brunaud V, Desnuelle C, Destée A, Dib M, Fleury MC, Furby A, Giroud M, Gonzales J, Guy N, Kolev I, Lacomblez L, Lardillier-Noel D, Le Forestier N, Maugin D, Nicolas G, Pittion S, Pouget J, Pradat PF, Rousso E, Salachas F, Soriani MH, Tranchant C, Vandenberghe N, Verschueren A, Viader F, Vial C. Meininger V, et al. Among authors: furby a. Rev Neurol (Paris). 2009 Mar;165(3):207-10. doi: 10.1016/j.neurol.2009.01.003. Epub 2009 Feb 12. Rev Neurol (Paris). 2009. PMID: 19217130 French. No abstract available.
PNPLA2 mutation: a paediatric case with early onset but indolent course.
Perrin L, Féasson L, Furby A, Laforêt P, Petit FM, Gautheron V, Chabrier S. Perrin L, et al. Among authors: furby a. Neuromuscul Disord. 2013 Dec;23(12):986-91. doi: 10.1016/j.nmd.2013.08.008. Epub 2013 Aug 30. Neuromuscul Disord. 2013. PMID: 24074500
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related Myopathies.
Villar-Quiles RN, Donkervoort S, de Becdelièvre A, Gartioux C, Jobic V, Foley AR, McCarty RM, Hu Y, Menassa R, Michel L, Gousse G, Lacour A, Petiot P, Streichenberger N, Choumert A, Declerck L, Urtizberea JA, Sole G, Furby A, Cérino M, Krahn M, Campana-Salort E, Ferreiro A, Eymard B, Bönnemann CG, Bharucha-Goebel D, Sumner CJ, Connolly AM, Richard P, Allamand V, Métay C, Stojkovic T. Villar-Quiles RN, et al. Among authors: furby a. J Neuromuscul Dis. 2021;8(4):633-645. doi: 10.3233/JND-200577. J Neuromuscul Dis. 2021. PMID: 33749658
In vivo and in vitro functional characterization of Andersen's syndrome mutations.
Bendahhou S, Fournier E, Sternberg D, Bassez G, Furby A, Sereni C, Donaldson MR, Larroque MM, Fontaine B, Barhanin J. Bendahhou S, et al. Among authors: furby a. J Physiol. 2005 Jun 15;565(Pt 3):731-41. doi: 10.1113/jphysiol.2004.081620. Epub 2005 Apr 14. J Physiol. 2005. PMID: 15831539 Free PMC article.
27 results