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Page 1
The multistep hypothesis of ALS revisited: The role of genetic mutations.
Chiò A, Mazzini L, D'Alfonso S, Corrado L, Canosa A, Moglia C, Manera U, Bersano E, Brunetti M, Barberis M, Veldink JH, van den Berg LH, Pearce N, Sproviero W, McLaughlin R, Vajda A, Hardiman O, Rooney J, Mora G, Calvo A, Al-Chalabi A. Chiò A, et al. Among authors: bersano e. Neurology. 2018 Aug 14;91(7):e635-e642. doi: 10.1212/WNL.0000000000005996. Epub 2018 Jul 25. Neurology. 2018. PMID: 30045958 Free PMC article.
Monomelic amyotrophy is not always benign: a case report.
Moglia C, Calvo A, Cammarosano S, Ilardi A, Canosa A, Gallo S, Bersano E, Chiò A. Moglia C, et al. Among authors: bersano e. Amyotroph Lateral Scler. 2011 Jul;12(4):307-8. doi: 10.3109/17482968.2011.560948. Epub 2011 Feb 23. Amyotroph Lateral Scler. 2011. PMID: 21344999
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations.
Chiò A, Restagno G, Brunetti M, Ossola I, Calvo A, Canosa A, Moglia C, Floris G, Tacconi P, Marrosu F, Marrosu MG, Murru MR, Majounie E, Renton AE, Abramzon Y, Pugliatti M, Sotgiu MA, Traynor BJ, Borghero G; SARDINIALS Consortium. Chiò A, et al. J Neurol Neurosurg Psychiatry. 2012 Jul;83(7):730-3. doi: 10.1136/jnnp-2012-302219. Epub 2012 May 1. J Neurol Neurosurg Psychiatry. 2012. PMID: 22550220 Free PMC article.
Amyotrophic lateral sclerosis/frontotemporal dementia with predominant manifestations of obsessive-compulsive disorder associated to GGGGCC expansion of the c9orf72 gene.
Calvo A, Moglia C, Canosa A, Cistaro A, Valentini C, Carrara G, Soldano E, Ilardi A, Bersano E, Bertuzzo D, Brunetti M, Ossola I, Restagno G, Chiò A. Calvo A, et al. Among authors: bersano e. J Neurol. 2012 Dec;259(12):2723-5. doi: 10.1007/s00415-012-6640-1. Epub 2012 Aug 24. J Neurol. 2012. PMID: 22918453 No abstract available.
Authors' response to a letter from Dr. Esquinas.
Olivieri C, Castioni CA, Livigni S, Bersano E, Cantello R, Della Corte F, Mazzini L. Olivieri C, et al. Among authors: bersano e. Acta Neurol Scand. 2014 May;129(5):e26. doi: 10.1111/ane.12242. Acta Neurol Scand. 2014. PMID: 24702473 No abstract available.
A rare case of conjugal amyotrophic lateral sclerosis.
Bersano E, Servo S, Cantello R, Mazzini L. Bersano E, et al. J Neurol. 2014 Jun;261(6):1216-7. doi: 10.1007/s00415-014-7330-y. Epub 2014 Apr 16. J Neurol. 2014. PMID: 24737169 No abstract available.
Amyotrophic lateral sclerosis outcome measures and the role of albumin and creatinine: a population-based study.
Chiò A, Calvo A, Bovio G, Canosa A, Bertuzzo D, Galmozzi F, Cugnasco P, Clerico M, De Mercanti S, Bersano E, Cammarosano S, Ilardi A, Manera U, Moglia C, Sideri R, Marinou K, Bottacchi E, Pisano F, Cantello R, Mazzini L, Mora G; Piemonte and Valle d’Aosta Register for Amyotrophic Lateral Sclerosis. Chiò A, et al. Among authors: bersano e. JAMA Neurol. 2014 Sep;71(9):1134-42. doi: 10.1001/jamaneurol.2014.1129. JAMA Neurol. 2014. PMID: 25048026 Free article.
ATXN2 polyQ intermediate repeats are a modifier of ALS survival.
Chiò A, Calvo A, Moglia C, Canosa A, Brunetti M, Barberis M, Restagno G, Conte A, Bisogni G, Marangi G, Moncada A, Lattante S, Zollino M, Sabatelli M, Bagarotti A, Corrado L, Mora G, Bersano E, Mazzini L, D'Alfonso S; PARALS. Chiò A, et al. Among authors: bersano e. Neurology. 2015 Jan 20;84(3):251-8. doi: 10.1212/WNL.0000000000001159. Epub 2014 Dec 19. Neurology. 2015. PMID: 25527265 Free article.
66 results