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Page 1
Vitamin D in amyotrophic lateral sclerosis.
Libonati L, Onesti E, Gori MC, Ceccanti M, Cambieri C, Fabbri A, Frasca V, Inghilleri M. Libonati L, et al. Funct Neurol. 2017 Jan/Mar;32(1):35-40. doi: 10.11138/fneur/2017.32.1.035. Funct Neurol. 2017. PMID: 28380322 Free PMC article.
Short-Term Ultramicronized Palmitoylethanolamide Therapy in Patients with Myasthenia Gravis: a Pilot Study to Possible Future Implications of Treatment.
Onesti E, Frasca V, Ceccanti M, Tartaglia G, Gori MC, Cambieri C, Libonati L, Palma E, Inghilleri M. Onesti E, et al. Among authors: libonati l. CNS Neurol Disord Drug Targets. 2019;18(3):232-238. doi: 10.2174/1871527318666190131121827. CNS Neurol Disord Drug Targets. 2019. PMID: 30706796 Clinical Trial.
A case of motor neuron involvement in Gaucher disease.
Pozzilli V, Giona F, Ceccanti M, Cambieri C, Frasca V, Onesti E, Libonati L, Di Bari S, Fiorini I, Cardarelli L, Santopietro M, Inghilleri M. Pozzilli V, et al. Among authors: libonati l. Mol Genet Metab Rep. 2019 Nov 12;21:100540. doi: 10.1016/j.ymgmr.2019.100540. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31844629 Free PMC article.
Creatine Kinase and Progression Rate in Amyotrophic Lateral Sclerosis.
Ceccanti M, Pozzilli V, Cambieri C, Libonati L, Onesti E, Frasca V, Fiorini I, Petrucci A, Garibaldi M, Palma E, Bendotti C, Fabbrizio P, Trolese MC, Nardo G, Inghilleri M. Ceccanti M, et al. Among authors: libonati l. Cells. 2020 May 8;9(5):1174. doi: 10.3390/cells9051174. Cells. 2020. PMID: 32397320 Free PMC article.
Validation of the DYALS (dysphagia in amyotrophic lateral sclerosis) questionnaire for the evaluation of dysphagia in ALS patients.
Diamanti L, Borrelli P, Dubbioso R, Capasso M, Morelli C, Lunetta C, Petrucci A, Mora G, Volanti P, Inghilleri M, Tremolizzo L, Mandrioli J, Mazzini L, Vedovello M, Siciliano G, Filosto M, Matà S, Montomoli C; DYALS Study Group. Diamanti L, et al. Neurol Sci. 2022 May;43(5):3195-3200. doi: 10.1007/s10072-021-05775-1. Epub 2021 Dec 1. Neurol Sci. 2022. PMID: 34853898
A novel homozygous mutation in TBK1 gene causing ALS-FTD.
Libonati L, Ceccanti M, Cambieri C, Colavito D, Moret F, Fiorini I, Inghilleri M. Libonati L, et al. Neurol Sci. 2022 Mar;43(3):2101-2104. doi: 10.1007/s10072-021-05820-z. Epub 2022 Jan 14. Neurol Sci. 2022. PMID: 35028775 No abstract available.
23 results