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Idiopathic generalized epilepsy in a family with SCN4A-related myotonia.
Talarico M, Fortunato F, Labalme A, Januel L, Chatron N, Sanlaville D, Sammarra I, Gagliardi M, Procopio R, Valentino P, Annesi G, Lesca G, Gambardella A. Talarico M, et al. Among authors: procopio r. Epilepsia Open. 2024 Jun;9(3):951-959. doi: 10.1002/epi4.12920. Epub 2024 Mar 27. Epilepsia Open. 2024. PMID: 38544349 Free PMC article.
A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.
Iannello G, Graziano C, Cenacchi G, Cordelli DM, Zuntini R, Papa V, Magistà AM, Gagliardi M, Procopio R, Quattrone A, Annesi G. Iannello G, et al. Among authors: procopio r. J Neurol Sci. 2017 Oct 15;381:209-212. doi: 10.1016/j.jns.2017.08.3260. Epub 2017 Sep 1. J Neurol Sci. 2017. PMID: 28991683
DNAJC13 mutation screening in patients with Parkinson's disease from South Italy.
Gagliardi M, Annesi G, Procopio R, Morelli M, Iannello G, Bonapace G, Mancini M, Nicoletti G, Quattrone A. Gagliardi M, et al. Among authors: procopio r. Parkinsonism Relat Disord. 2018 Oct;55:134-137. doi: 10.1016/j.parkreldis.2018.06.004. Epub 2018 Jun 4. Parkinsonism Relat Disord. 2018. PMID: 29887357
Analysis of the TMEM230 gene in patients with multiple system atrophy.
Procopio R, Gagliardi M, Brighina L, Nicoletti G, Morelli M, Piatti M, Annesi G, Quattrone A. Procopio R, et al. J Neurol Sci. 2018 Sep 15;392:128-129. doi: 10.1016/j.jns.2018.07.019. Epub 2018 Jul 23. J Neurol Sci. 2018. PMID: 30056200 No abstract available.
79 results