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No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype.
Bertolin C, Querin G, Da Re E, Sagnelli A, Bello L, Cao M, Muscas M, Pennuto M, Ermani M, Pegoraro E, Mariotti C, Gellera C, Hanna MG, Pareyson D, Fratta P, Sorarù G. Bertolin C, et al. Among authors: sagnelli a. Eur J Neurol. 2016 Jun;23(6):1134-6. doi: 10.1111/ene.13001. Eur J Neurol. 2016. PMID: 27141859
Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients.
Querin G, Bertolin C, Da Re E, Volpe M, Zara G, Pegoraro E, Caretta N, Foresta C, Silvano M, Corrado D, Iafrate M, Angelini L, Sartori L, Pennuto M, Gaiani A, Bello L, Semplicini C, Pareyson D, Silani V, Ermani M, Ferlin A, Sorarù G; Italian Study Group on Kennedy's disease. Querin G, et al. J Neurol Neurosurg Psychiatry. 2016 Aug;87(8):810-6. doi: 10.1136/jnnp-2015-311305. Epub 2015 Oct 26. J Neurol Neurosurg Psychiatry. 2016. PMID: 26503015 Free PMC article.
Inherited neuropathies: an update.
Sagnelli A, Piscosquito G, Pareyson D. Sagnelli A, et al. J Neurol. 2013 Oct;260(10):2684-90. doi: 10.1007/s00415-013-7113-x. Epub 2013 Sep 24. J Neurol. 2013. PMID: 24061768 Review.
Human adipose-derived mesenchymal stem cells as a new model of spinal and bulbar muscular atrophy.
Dossena M, Bedini G, Rusmini P, Giorgetti E, Canazza A, Tosetti V, Salsano E, Sagnelli A, Mariotti C, Gellera C, Navone SE, Marfia G, Alessandri G, Corsi F, Parati EA, Pareyson D, Poletti A. Dossena M, et al. Among authors: sagnelli a. PLoS One. 2014 Nov 13;9(11):e112746. doi: 10.1371/journal.pone.0112746. eCollection 2014. PLoS One. 2014. PMID: 25392924 Free PMC article.
Mitochondrial dynamics and inherited peripheral nerve diseases.
Pareyson D, Saveri P, Sagnelli A, Piscosquito G. Pareyson D, et al. Among authors: sagnelli a. Neurosci Lett. 2015 Jun 2;596:66-77. doi: 10.1016/j.neulet.2015.04.001. Epub 2015 Apr 3. Neurosci Lett. 2015. PMID: 25847151 Review.
27 results