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

Year Number of Results
2001 1
2002 1
2009 1
2013 1
2014 2
2016 4
2018 1
2019 4
2020 1
2021 2
2022 3
2023 1
2024 1

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21 results

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Page 1
Genome editing in primary cells and in vivo using viral-derived Nanoblades loaded with Cas9-sgRNA ribonucleoproteins.
Mangeot PE, Risson V, Fusil F, Marnef A, Laurent E, Blin J, Mournetas V, Massouridès E, Sohier TJM, Corbin A, Aubé F, Teixeira M, Pinset C, Schaeffer L, Legube G, Cosset FL, Verhoeyen E, Ohlmann T, Ricci EP. Mangeot PE, et al. Among authors: risson v. Nat Commun. 2019 Jan 3;10(1):45. doi: 10.1038/s41467-018-07845-z. Nat Commun. 2019. PMID: 30604748 Free PMC article.
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.
Jacquier A, Risson V, Simonet T, Roussange F, Lacoste N, Ribault S, Carras J, Theuriet J, Girard E, Grosjean I, Le Goff L, Kröger S, Meltoranta J, Bauché S, Sternberg D, Fournier E, Kostera-Pruszczyk A, O'Connor E, Eymard B, Lochmüller H, Martinat C, Schaeffer L. Jacquier A, et al. Among authors: risson v. Acta Neuropathol. 2022 Oct;144(4):707-731. doi: 10.1007/s00401-022-02475-8. Epub 2022 Aug 10. Acta Neuropathol. 2022. PMID: 35948834 Free PMC article.
Anti-agrin autoantibodies in myasthenia gravis.
Gasperi C, Melms A, Schoser B, Zhang Y, Meltoranta J, Risson V, Schaeffer L, Schalke B, Kröger S. Gasperi C, et al. Among authors: risson v. Neurology. 2014 Jun 3;82(22):1976-83. doi: 10.1212/WNL.0000000000000478. Epub 2014 May 2. Neurology. 2014. PMID: 24793185
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy.
Jacquier A, Theuriet J, Fontaine F, Mosbach V, Lacoste N, Ribault S, Risson V, Carras J, Coudert L, Simonet T, Latour P, Stojkovic T, Piard J, Cosson A, Lesca G, Bouhour F, Allouche S, Puccio H, Pegat A, Schaeffer L. Jacquier A, et al. Among authors: risson v. Brain. 2023 Aug 1;146(8):3470-3483. doi: 10.1093/brain/awac453. Brain. 2023. PMID: 36454683 Free PMC article.
Antibodies to clustered acetylcholine receptor: expanding the phenotype.
Devic P, Petiot P, Simonet T, Stojkovic T, Delmont E, Franques J, Magot A, Vial C, Lagrange E, Nicot AS, Risson V, Eymard B, Schaeffer L. Devic P, et al. Among authors: risson v. Eur J Neurol. 2014;21(1):130-4. doi: 10.1111/ene.12270. Epub 2013 Sep 21. Eur J Neurol. 2014. PMID: 24112557
Modelling Decline in Cognition to Decline in Function in Alzheimer's Disease.
Karcher H, Savelieva M, Qi L, Hummel N, Caputo A, Risson V, Capkun G, Alzheimer's Disease Neuroimaging Initiative. Karcher H, et al. Among authors: risson v. Curr Alzheimer Res. 2020;17(7):635-657. doi: 10.2174/1567205017666201008105429. Curr Alzheimer Res. 2020. PMID: 33032508
21 results