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Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern France.
Davion JB, Bocquillon P, Cassim F, Frezel N, Lacour A, Dhaenens CM, Maurage CA, Gibier JB, Hachulla E, Nguyen The Tich S, Defebvre L, Merle PE, Tard C. Davion JB, et al. Rev Neurol (Paris). 2021 Nov;177(9):1160-1167. doi: 10.1016/j.neurol.2021.02.392. Epub 2021 Jul 10. Rev Neurol (Paris). 2021. PMID: 34253345
Diaphragmatic weakness related to radiotherapy: 2 cases and a review.
Davion JB, Duthoit L, Starzyńska-Kubicka A, Perez T, Bocquillon P, Defebvre L, Nguyen The Tich S, Lefebvre G, Tard C. Davion JB, et al. Rev Neurol (Paris). 2022 Oct;178(8):796-801. doi: 10.1016/j.neurol.2022.02.459. Epub 2022 Jun 9. Rev Neurol (Paris). 2022. PMID: 35690475
Real-world multidisciplinary outcomes of onasemnogene abeparvovec monotherapy in patients with spinal muscular atrophy type 1: experience of the French cohort in the first three years of treatment.
Desguerre I, Barrois R, Audic F, Barnerias C, Chabrol B, Davion JB, Durigneux J, Espil-Taris C, Gomez-Garcia de la Banda M, Guichard M, Isapof A, Nougues MC, Laugel V, Le Goff L, Mercier S, Pervillé A, Richelme C, Thibaud M, Sarret C, Schweitzer C, Testard H, Trommsdorff V, Vanhulle C, Walther-Louvier U, Altuzarra C, Chouchane M, Ropars J, Quijano-Roy S, Cances C. Desguerre I, et al. Among authors: davion jb. Orphanet J Rare Dis. 2024 Sep 13;19(1):344. doi: 10.1186/s13023-024-03326-3. Orphanet J Rare Dis. 2024. PMID: 39272200 Free PMC article.
36 results