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

Year Number of Results
1999 1
2005 1
2006 1
2012 3
2013 1
2014 2
2015 2
2016 1
2017 1
2018 1
2019 2
2020 2
2021 1
2023 1
2024 1

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Page 1
Distinct neurological disorders with ATP1A3 mutations.
Heinzen EL, Arzimanoglou A, Brashear A, Clapcote SJ, Gurrieri F, Goldstein DB, Jóhannesson SH, Mikati MA, Neville B, Nicole S, Ozelius LJ, Poulsen H, Schyns T, Sweadner KJ, van den Maagdenberg A, Vilsen B; ATP1A3 Working Group. Heinzen EL, et al. Lancet Neurol. 2014 May;13(5):503-14. doi: 10.1016/S1474-4422(14)70011-0. Lancet Neurol. 2014. PMID: 24739246 Free PMC article. Review.
Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?
Pera MC, Coratti G, Berti B, D'Amico A, Sframeli M, Albamonte E, de Sanctis R, Messina S, Catteruccia M, Brigati G, Antonaci L, Lucibello S, Bruno C, Sansone VA, Bertini E, Tiziano D, Pane M, Mercuri E. Pera MC, et al. Among authors: tiziano d. PLoS One. 2020 Mar 23;15(3):e0230677. doi: 10.1371/journal.pone.0230677. eCollection 2020. PLoS One. 2020. PMID: 32203538 Free PMC article.
Developmental milestones in type I spinal muscular atrophy.
De Sanctis R, Coratti G, Pasternak A, Montes J, Pane M, Mazzone ES, Young SD, Salazar R, Quigley J, Pera MC, Antonaci L, Lapenta L, Glanzman AM, Tiziano D, Muntoni F, Darras BT, De Vivo DC, Finkel R, Mercuri E. De Sanctis R, et al. Among authors: tiziano d. Neuromuscul Disord. 2016 Nov;26(11):754-759. doi: 10.1016/j.nmd.2016.10.002. Epub 2016 Oct 5. Neuromuscul Disord. 2016. PMID: 27769560 Free PMC article.
Gene targeting restricted to mouse striated muscle lineage.
Miniou P, Tiziano D, Frugier T, Roblot N, Le Meur M, Melki J. Miniou P, et al. Among authors: tiziano d. Nucleic Acids Res. 1999 Oct 1;27(19):e27. doi: 10.1093/nar/27.19.e27. Nucleic Acids Res. 1999. PMID: 10481039 Free PMC article.
17 results