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21 results

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Page 1
A new truncating MPZ mutation associated with a very mild CMT1 B phenotype.
Piazza S, Baldinotti F, Fogli A, Conidi ME, Michelucci A, Ienco EC, Mancuso M, Simi P, Siciliano G. Piazza S, et al. Among authors: ienco ec. Neuromuscul Disord. 2010 Dec;20(12):817-9. doi: 10.1016/j.nmd.2010.08.003. Epub 2010 Sep 17. Neuromuscul Disord. 2010. PMID: 20850974
An "inflammatory" mitochondrial myopathy. A case report.
Mancuso M, Orsucci D, Ienco EC, Ricci G, Ali G, Servadio A, Fontanini G, Filosto M, Vielmi V, Rocchi A, Petrozzi L, Logerfo A, Siciliano G. Mancuso M, et al. Among authors: ienco ec. Neuromuscul Disord. 2013 Nov;23(11):907-10. doi: 10.1016/j.nmd.2013.07.011. Epub 2013 Aug 8. Neuromuscul Disord. 2013. PMID: 24011700
"Mitochondrial neuropathies": A survey from the large cohort of the Italian Network.
Mancuso M, Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Federico A, Minetti C, Moggio M, Mongini T, Tonin P, Toscano A, Bruno C, Ienco EC, Filosto M, Lamperti C, Diodato D, Moroni I, Musumeci O, Pegoraro E, Spinazzi M, Ahmed N, Sciacco M, Vercelli L, Ardissone A, Zeviani M, Siciliano G. Mancuso M, et al. Among authors: ienco ec. Neuromuscul Disord. 2016 Apr-May;26(4-5):272-6. doi: 10.1016/j.nmd.2016.02.008. Epub 2016 Feb 23. Neuromuscul Disord. 2016. PMID: 27020842 Free article.
Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany.
Orsucci D, Petrucci L, Ienco EC, Chico L, Simi P, Fogli A, Baldinotti F, Simoncini C, LoGerfo A, Carlesi C, Arnoldi A, Bassi MT, Siciliano G, Bonuccelli U, Mancuso M. Orsucci D, et al. Among authors: ienco ec. Clin Neurol Neurosurg. 2014 May;120:14-9. doi: 10.1016/j.clineuro.2014.02.002. Epub 2014 Feb 17. Clin Neurol Neurosurg. 2014. PMID: 24731568
Levetiracetam-responsive myoclonus in spinocerebellar ataxia type 15.
Orsucci D, Ienco EC, Rocchi A, Siciliano G, Mancuso M, Bonuccelli U. Orsucci D, et al. Among authors: ienco ec. Mov Disord. 2013 Sep;28(10):1465. doi: 10.1002/mds.25433. Epub 2013 Mar 14. Mov Disord. 2013. PMID: 23495097 No abstract available.
Amyotrophic Lateral Sclerosis: A Genetic Point of View.
Carlesi C, Ienco EC, Mancuso M, Siciliano G. Carlesi C, et al. Among authors: ienco ec. Curr Mol Med. 2014;14(8):1089-1101. doi: 10.2174/1566524014666141010155822. Curr Mol Med. 2014. PMID: 25323864
21 results