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

Year Number of Results
1985 1
1986 2
1987 4
1988 4
1989 2
1991 5
1992 5
1993 7
1994 6
1995 8
1996 11
1997 4
1998 8
1999 3
2000 12
2001 14
2002 14
2003 15
2004 22
2005 18
2006 11
2007 6
2008 10
2009 5
2010 13
2011 7
2012 9
2013 18
2014 18
2015 18
2016 13
2017 8
2018 4
2019 2
2020 8
2021 4
2023 6
2024 0

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300 results

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Page 1
Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial.
McDonald CM, Campbell C, Torricelli RE, Finkel RS, Flanigan KM, Goemans N, Heydemann P, Kaminska A, Kirschner J, Muntoni F, Osorio AN, Schara U, Sejersen T, Shieh PB, Sweeney HL, Topaloglu H, Tulinius M, Vilchez JJ, Voit T, Wong B, Elfring G, Kroger H, Luo X, McIntosh J, Ong T, Riebling P, Souza M, Spiegel RJ, Peltz SW, Mercuri E; Clinical Evaluator Training Group; ACT DMD Study Group. McDonald CM, et al. Among authors: voit t. Lancet. 2017 Sep 23;390(10101):1489-1498. doi: 10.1016/S0140-6736(17)31611-2. Epub 2017 Jul 17. Lancet. 2017. PMID: 28728956 Clinical Trial.
Classic in neuropediatrics.
Voit T. Voit T. Neuropediatrics. 2001 Dec;32(6):277-8. doi: 10.1055/s-2001-20401. Neuropediatrics. 2001. PMID: 11870581 No abstract available.
Adult polyglucosan body myopathy.
Goebel HH, Shin YS, Gullotta F, Yokota T, Alroy J, Voit T, Haller P, Schulz A. Goebel HH, et al. Among authors: voit t. J Neuropathol Exp Neurol. 1992 Jan;51(1):24-35. doi: 10.1097/00005072-199201000-00004. J Neuropathol Exp Neurol. 1992. PMID: 1311021 Review.
From adhalinopathies to alpha-sarcoglycanopathies: an overview.
Jeanpierre M, Carrié A, Piccolo F, Leturcq F, Azibi K, De Toma C, Beldjord C, Merlini L, Voit T, Romero N, Sunada Y, Tomé FM, Fardeau M, Campbell KP, Kaplan JC. Jeanpierre M, et al. Among authors: voit t. Neuromuscul Disord. 1996 Dec;6(6):463-5. doi: 10.1016/s0960-8966(96)00394-x. Neuromuscul Disord. 1996. PMID: 9027856 Review. No abstract available.
300 results