Prada V - Search Results

1

Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype.

Callegari I, Gemelli C, Geroldi A, Veneri F, Mandich P, D'Antonio M, Pareyson D, Shy ME, Schenone A, Prada V, Grandis M. Callegari I, et al. Among authors: prada v. J Neurol. 2019 Nov;266(11):2629-2645. doi: 10.1007/s00415-019-09453-3. Epub 2019 Jul 5. J Neurol. 2019. PMID: 31278453

2

Gain of glycosylation: a new pathomechanism of myelin protein zero mutations.

Prada V, Passalacqua M, Bono M, Luzzi P, Scazzola S, Nobbio LA, Capponi S, Bellone E, Mandich P, Mancardi G, Shy M, Schenone A, Grandis M. Prada V, et al. Ann Neurol. 2012 Mar;71(3):427-31. doi: 10.1002/ana.22695. Ann Neurol. 2012. PMID: 22451207 Free PMC article.

3

The diadenosine homodinucleotide P18 improves in vitro myelination in experimental Charcot-Marie-Tooth type 1A.

Nobbio L, Visigalli D, Mannino E, Fiorese F, Kassack MU, Sturla L, Prada V, De Flora A, Zocchi E, Bruzzone S, Schenone A. Nobbio L, et al. Among authors: prada v. J Cell Biochem. 2014 Jan;115(1):161-7. doi: 10.1002/jcb.24644. J Cell Biochem. 2014. PMID: 23959806 Free article.

4

Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation.

Prada V, Capponi S, Ursino G, Alberti A, Callegari I, Passalacqua M, Marotta R, Mandich P, Bellone E, Schenone A, Grandis M. Prada V, et al. Neuropathology. 2015 Jun;35(3):254-9. doi: 10.1111/neup.12179. Epub 2014 Nov 11. Neuropathology. 2015. PMID: 25388615

5

Innovative quantitative testing of hand function in Charcot-Marie-Tooth neuropathy.

Alberti MA, Mori L, Francini L, Poggi I, Monti Bragadin M, Bellone E, Grandis M, Maggi G, Reni L, Sormani MP, Tacchino A, Padua L, Prada V, Bove M, Schenone A. Alberti MA, et al. Among authors: prada v. J Peripher Nerv Syst. 2015 Dec;20(4):410-4. doi: 10.1111/jns.12150. J Peripher Nerv Syst. 2015. PMID: 26456943

6

Testing overwork weakness in Charcot-Marie-tooth disease: Is it true or false?

Prada V, Mori L, Accogli S, Rivarola M, Schizzi S, Hamedani M, Schenone A. Prada V, et al. J Peripher Nerv Syst. 2018 Jun;23(2):124-128. doi: 10.1111/jns.12270. Epub 2018 May 7. J Peripher Nerv Syst. 2018. PMID: 29693294

7

Outcome measures in the clinical evaluation of ambulatory Charcot-Marie-Tooth 1A subjects.

Mori L, Prada V, Signori A, Pareyson D, Piscosquito G, Padua L, Pazzaglia C, Fabrizi GM, Smania N, Picelli A, Schenone A; TreSPE Study Group. Mori L, et al. Among authors: prada v. Eur J Phys Rehabil Med. 2019 Feb;55(1):47-55. doi: 10.23736/S1973-9087.18.05111-0. Epub 2018 Jun 11. Eur J Phys Rehabil Med. 2019. PMID: 29898585 Free article. Clinical Trial.

8

A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea.

Bommarito G, Cellerino M, Prada V, Venturi C, Capellari S, Cortelli P, Mancardi GL, Parchi P, Schenone A. Bommarito G, et al. Among authors: prada v. Eur J Neurol. 2018 Aug;25(8):e91-e92. doi: 10.1111/ene.13665. Eur J Neurol. 2018. PMID: 29984897 No abstract available.

9

Hand Rehabilitation Treatment for Charcot-Marie-Tooth Disease: An Open Label Pilot Study.

Prada V, Schizzi S, Poggi I, Mori L, Gemelli C, Hamedani M, Accogli S, Maggi G, Grandis M, Mancardi GL, Schenone A. Prada V, et al. J Neurol Neurophysiol. 2018 Jul 30;9(4):465. doi: 10.4172/2155-9562.1000465. J Neurol Neurophysiol. 2018. PMID: 30305981 Free PMC article.

10

A novel mutation in the N-terminal acting-binding domain of Filamin C protein causing a distal myofibrillar myopathy.

Gemelli C, Prada V, Fiorillo C, Fabbri S, Maggi L, Geroldi A, Gibertini S, Mandich P, Trevisan L, Fossa P, Tagliafico AS, Schenone A, Grandis M. Gemelli C, et al. Among authors: prada v. J Neurol Sci. 2019 Mar 15;398:75-78. doi: 10.1016/j.jns.2019.01.019. Epub 2019 Jan 17. J Neurol Sci. 2019. PMID: 30685713

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