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329 results

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Page 1
Subacute combined degeneration.
Luigetti M, Pravatà E, Bernardo D, Izzo MG, Servidei S. Luigetti M, et al. Among authors: bernardo d. Acta Neurol Belg. 2014 Sep;114(3):221-2. doi: 10.1007/s13760-013-0231-5. Epub 2013 Jul 11. Acta Neurol Belg. 2014. PMID: 23843196 No abstract available.
Erratum to "Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience" [Clin. Neurol. Neurosurg. 144 (2016) 67-71].
Luigetti M, Fabrizi GM, Bisogni G, Romano A, Taioli F, Ferrarini M, Bernardo D, Rossini PM, Sabatelli M. Luigetti M, et al. Among authors: bernardo d. Clin Neurol Neurosurg. 2016 Jun 2:S0303-8467(16)30182-2. doi: 10.1016/j.clineuro.2016.05.011. Online ahead of print. Clin Neurol Neurosurg. 2016. PMID: 27265096 No abstract available.
Mitochondrial neuropathy: considerations on pathogenesis.
Luigetti M, Sauchelli D, Primiano G, Cuccagna C, Bernardo D, Lo Monaco M, Servidei S. Luigetti M, et al. Among authors: bernardo d. Eur J Neurol. 2016 Aug;23(8):e55. doi: 10.1111/ene.13049. Eur J Neurol. 2016. PMID: 27431029 No abstract available.
Small fibre neuropathy in mitochondrial diseases explored with sudoscan.
Luigetti M, Primiano G, Cuccagna C, Bernardo D, Sauchelli D, Vollono C, Servidei S. Luigetti M, et al. Among authors: bernardo d. Clin Neurophysiol. 2018 Aug;129(8):1618-1623. doi: 10.1016/j.clinph.2018.04.755. Epub 2018 Jun 1. Clin Neurophysiol. 2018. PMID: 29890373
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS.
Lattante S, Doronzio PN, Marangi G, Conte A, Bisogni G, Bernardo D, Russo T, Lamberti D, Patrizi S, Apollo FP, Lunetta C, Scarlino S, Pozzi L, Zollino M, Riva N, Sabatelli M. Lattante S, et al. Among authors: bernardo d. Neurobiol Aging. 2019 Dec;84:239.e9-239.e14. doi: 10.1016/j.neurobiolaging.2019.03.010. Epub 2019 Mar 27. Neurobiol Aging. 2019. PMID: 31000212
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study.
Adams D, Polydefkis M, González-Duarte A, Wixner J, Kristen AV, Schmidt HH, Berk JL, Losada López IA, Dispenzieri A, Quan D, Conceição IM, Slama MS, Gillmore JD, Kyriakides T, Ajroud-Driss S, Waddington-Cruz M, Mezei MM, Planté-Bordeneuve V, Attarian S, Mauricio E, Brannagan TH 3rd, Ueda M, Aldinc E, Wang JJ, White MT, Vest J, Berber E, Sweetser MT, Coelho T; patisiran Global OLE study group. Adams D, et al. Lancet Neurol. 2021 Jan;20(1):49-59. doi: 10.1016/S1474-4422(20)30368-9. Epub 2020 Nov 16. Lancet Neurol. 2021. PMID: 33212063 Clinical Trial.
329 results