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

Year Number of Results
1995 1
1996 3
1997 2
1999 1
2001 1
2002 2
2003 3
2004 3
2005 3
2006 5
2007 6
2008 2
2009 5
2010 5
2011 1
2012 5
2013 2
2015 4
2017 1
2020 1
2022 0
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52 results
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Page 1
Resistance strength training exercise in children with spinal muscular atrophy.
Lewelt A, Krosschell KJ, Stoddard GJ, Weng C, Xue M, Marcus RL, Gappmaier E, Viollet L, Johnson BA, White AT, Viazzo-Trussell D, Lopes P, Lane RH, Carey JC, Swoboda KJ. Lewelt A, et al. Among authors: viollet l. Muscle Nerve. 2015 Oct;52(4):559-67. doi: 10.1002/mus.24568. Muscle Nerve. 2015. PMID: 25597614 Free PMC article.
Spinal muscular atrophies.
Viollet L, Melki J. Viollet L, et al. Handb Clin Neurol. 2013;113:1395-411. doi: 10.1016/B978-0-444-59565-2.00010-1. Handb Clin Neurol. 2013. PMID: 23622363 Review.
HIV-1 triggers mitochondrion death.
Arnoult D, Viollet L, Petit F, Lelièvre JD, Estaquier J. Arnoult D, et al. Among authors: viollet l. Mitochondrion. 2004 Jul;4(2-3):255-69. doi: 10.1016/j.mito.2004.06.010. Mitochondrion. 2004. PMID: 16120390
Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiency.
Prando C, Boisson-Dupuis S, Grant AV, Kong XF, Bustamante J, Feinberg J, Chapgier A, Rose Y, Jannière L, Rizzardi E, Zhang Q, Shanahan CM, Viollet L, Lyonnet S, Abel L, Ruga EM, Casanova JL. Prando C, et al. Among authors: viollet l. Am J Med Genet A. 2010 Mar;152A(3):622-9. doi: 10.1002/ajmg.a.33291. Am J Med Genet A. 2010. PMID: 20186794 Free PMC article. Review.
Evoked potentials in spinal muscular atrophy.
Cheliout-Heraut F, Barois A, Urtizberea A, Viollet L, Estournet-Mathiaud B. Cheliout-Heraut F, et al. Among authors: viollet l. J Child Neurol. 2003 Jun;18(6):383-90. doi: 10.1177/08830738030180061101. J Child Neurol. 2003. PMID: 12886971
Riluzole pharmacokinetics in young patients with spinal muscular atrophy.
Abbara C, Estournet B, Lacomblez L, Lelièvre B, Ouslimani A, Lehmann B, Viollet L, Barois A, Diquet B. Abbara C, et al. Among authors: viollet l. Br J Clin Pharmacol. 2011 Mar;71(3):403-10. doi: 10.1111/j.1365-2125.2010.03843.x. Br J Clin Pharmacol. 2011. PMID: 21284699 Free PMC article. Clinical Trial.
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies.
Viollet LM, Swoboda KJ, Mao R, Best H, Ha Y, Toutain A, Guyant-Marechal L, Laroche-Raynaud C, Ghorab K, Barthez MA, Pedespan JM, Hernandorena X, Lia AS, Deleuze JF, Masson C, Nelson I, Nectoux J, Si Y. Viollet LM, et al. Eur J Med Genet. 2020 Dec;63(12):104063. doi: 10.1016/j.ejmg.2020.104063. Epub 2020 Sep 16. Eur J Med Genet. 2020. PMID: 32947049
Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders.
Rosewich H, Sweney MT, DeBrosse S, Ess K, Ozelius L, Andermann E, Andermann F, Andrasco G, Belgrade A, Brashear A, Ciccodicola S, Egan L, George AL Jr, Lewelt A, Magelby J, Merida M, Newcomb T, Platt V, Poncelin D, Reyna S, Sasaki M, Sotero de Menezes M, Sweadner K, Viollet L, Zupanc M, Silver K, Swoboda K. Rosewich H, et al. Among authors: viollet l. Neurol Genet. 2017 Mar 2;3(2):e139. doi: 10.1212/NXG.0000000000000139. eCollection 2017 Apr. Neurol Genet. 2017. PMID: 28293679 Free PMC article.
52 results