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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 6
2010 5
2011 2
2012 6
2013 4
2015 4
2017 1
2020 1
2023 1
2024 0

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58 results

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Page 1
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.
Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Gappmaier E, Howard MT, Sampson JB, Mendell JR, Wall C, King WM, Pestronk A, Florence JM, Connolly AM, Mathews KD, Stephan CM, Laubenthal KS, Wong BL, Morehart PJ, Meyer A, Finkel RS, Bonnemann CG, Medne L, Day JW, Dalton JC, Margolis MK, Hinton VJ; United Dystrophinopathy Project Consortium; Weiss RB. Flanigan KM, et al. Hum Mutat. 2009 Dec;30(12):1657-66. doi: 10.1002/humu.21114. Hum Mutat. 2009. PMID: 19937601 Free PMC article.
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.
TANGO: a placebo-controlled randomized phase 2 study of efficacy and safety of the anti-tau monoclonal antibody gosuranemab in early Alzheimer's disease.
Shulman M, Kong J, O'Gorman J, Ratti E, Rajagovindan R, Viollet L, Huang E, Sharma S, Racine AM, Czerkowicz J, Graham D, Li Y, Hering H, Haeberlein SB. Shulman M, et al. Among authors: viollet l. Nat Aging. 2023 Dec;3(12):1591-1601. doi: 10.1038/s43587-023-00523-w. Epub 2023 Nov 27. Nat Aging. 2023. PMID: 38012285 Free PMC article. Clinical Trial.
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
58 results