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Page 1
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
Linked Patient-Reported Outcomes Data From Patients With Multiple Sclerosis Recruited on an Open Internet Platform to Health Care Claims Databases Identifies a Representative Population for Real-Life Data Analysis in Multiple Sclerosis.
Risson V, Ghodge B, Bonzani IC, Korn JR, Medin J, Saraykar T, Sengupta S, Saini D, Olson M. Risson V, et al. J Med Internet Res. 2016 Sep 22;18(9):e249. doi: 10.2196/jmir.5805. J Med Internet Res. 2016. PMID: 27658498 Free PMC article.
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.
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.
22 results