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Improvement of Charcot-Marie-Tooth Phenotype with a Nanocomplex Treatment in Two Transgenic Models of CMT1A.
El Massry M, Msheik Z, El Masri T, Ntoutoume GMN, Vignaud L, Richard L, Pinault E, Faye PA, Bregier F, Marquet P, Favreau F, Vallat JM, Billet F, Sol V, Sturtz F, Desmouliere A. El Massry M, et al. Among authors: vallat jm. Biomater Res. 2024 Mar 28;28:0009. doi: 10.34133/bmr.0009. eCollection 2024. Biomater Res. 2024. PMID: 38560579 Free PMC article.
Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation.
Lemerle E, Lainé J, Benoist M, Moulay G, Bigot A, Labasse C, Madelaine A, Canette A, Aubin P, Vallat JM, Romero NB, Bitoun M, Mouly V, Marty I, Cadot B, Picas L, Vassilopoulos S. Lemerle E, et al. Among authors: vallat jm. Elife. 2023 Apr 21;12:e84139. doi: 10.7554/eLife.84139. Elife. 2023. PMID: 37083699 Free PMC article.
Early Diagnosis in Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (CANVAS) by Focusing on Major Clinical Clues: Beyond Ataxia and Vestibular Impairment.
Magy L, Chazelas P, Richard L, Deschamps N, Frachet S, Vallat JM, Magdelaine C, Favreau F, Bessaguet F, Lia AS, Duchesne M. Magy L, et al. Among authors: vallat jm. Biomedicines. 2022 Aug 22;10(8):2046. doi: 10.3390/biomedicines10082046. Biomedicines. 2022. PMID: 36009593 Free PMC article.
A novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism.
Veneri FA, Prada V, Mastrangelo R, Ferri C, Nobbio L, Passalacqua M, Milanesi M, Bianchi F, Del Carro U, Vallat JM, Duong P, Svaren J, Schenone A, Grandis M, D'Antonio M. Veneri FA, et al. Among authors: vallat jm. Hum Mol Genet. 2022 Dec 16;31(24):4255-4274. doi: 10.1093/hmg/ddac170. Hum Mol Genet. 2022. PMID: 35908287 Free PMC article.
Are Miller Fisher syndrome and CANDA due to a paranodopathy?
Vallat JM, Deschamps N, Taithe F, Richard L, Duchesne M, Magy L, Mathis S. Vallat JM, et al. J Neurol Sci. 2022 Jul 15;438:120279. doi: 10.1016/j.jns.2022.120279. Epub 2022 May 10. J Neurol Sci. 2022. PMID: 35576641
476 results