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Charcot-Marie-Tooth Disease with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber Neuropathy.
Int J Mol Sci. 2024 Jan 29;25(3):1654. doi: 10.3390/ijms25031654.
Int J Mol Sci. 2024.
PMID: 38338934
Free PMC article.
Effect of tauroursodeoxycholic acid on survival and safety in amyotrophic lateral sclerosis: a retrospective population-based cohort study.
Zucchi E, Musazzi UM, Fedele G, Martinelli I, Gianferrari G, Simonini C, Fini N, Ghezzi A, Caputo M, Sette E, Vacchiano V, Zinno L, Anceschi P, Canali E, Vinceti M, Ferro S, Mandrioli J; ERRALS study group.
Zucchi E, et al.
EClinicalMedicine. 2023 Oct 5;65:102256. doi: 10.1016/j.eclinm.2023.102256. eCollection 2023 Nov.
EClinicalMedicine. 2023.
PMID: 37842553
Free PMC article.
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Correction to: Retrospective observational study on the use of acetyl-L-carnitine in ALS.
Sassi S, Bianchi E, Diamanti L, Tornabene D, Sette E, Medici D, Matà S, Leccese D, Sperti M, Martinelli I, Ghezzi A, Mandrioli J, Iuzzolino VV, Dubbioso R, Trojsi F, Passaniti C, D'Alvano G, Filosto M, Padovani A, Mazzini L, De Marchi F, Zinno L, Nuredini A, Bongioanni P, Dolciotti C, Canali E, Toschi G, Petrucci A, Perna A, Riso V, Inghilleri M, Libonati L, Cambieri C, Pupillo E.
Sassi S, et al. Among authors: nuredini a.
J Neurol. 2023 Nov;270(11):5358-5359. doi: 10.1007/s00415-023-11960-3.
J Neurol. 2023.
PMID: 37682317
Free PMC article.
No abstract available.
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Retrospective observational study on the use of acetyl-L-carnitine in ALS.
Sassi S, Bianchi E, Diamanti L, Tornabene D, Sette E, Medici D, Matà S, Leccese D, Sperti M, Martinelli I, Ghezzi A, Mandrioli J, Iuzzolino VV, Dubbioso R, Trojsi F, Passaniti C, D'Alvano G, Filosto M, Padovani A, Mazzini L, De Marchi F, Zinno L, Nuredini A, Bongioanni P, Dolciotti C, Canali E, Toschi G, Petrucci A, Perna A, Riso V, Inghilleri M, Libonati L, Cambieri C, Pupillo E.
Sassi S, et al. Among authors: nuredini a.
J Neurol. 2023 Nov;270(11):5344-5357. doi: 10.1007/s00415-023-11844-6. Epub 2023 Jun 28.
J Neurol. 2023.
PMID: 37378756
Free PMC article.
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Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne Muscular Dystrophy: The Issue of Transgene Persistence.
Manini A, Abati E, Nuredini A, Corti S, Comi GP.
Manini A, et al. Among authors: nuredini a.
Front Neurol. 2022 Jan 5;12:814174. doi: 10.3389/fneur.2021.814174. eCollection 2021.
Front Neurol. 2022.
PMID: 35095747
Free PMC article.
Review.
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