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Exome sequencing reveals VCP mutations as a cause of familial ALS.
Johnson JO, Mandrioli J, Benatar M, Abramzon Y, Van Deerlin VM, Trojanowski JQ, Gibbs JR, Brunetti M, Gronka S, Wuu J, Ding J, McCluskey L, Martinez-Lage M, Falcone D, Hernandez DG, Arepalli S, Chong S, Schymick JC, Rothstein J, Landi F, Wang YD, Calvo A, Mora G, Sabatelli M, Monsurrò MR, Battistini S, Salvi F, Spataro R, Sola P, Borghero G; ITALSGEN Consortium; Galassi G, Scholz SW, Taylor JP, Restagno G, Chiò A, Traynor BJ. Johnson JO, et al. Among authors: galassi g. Neuron. 2010 Dec 9;68(5):857-64. doi: 10.1016/j.neuron.2010.11.036. Neuron. 2010. PMID: 21145000 Free PMC article.
Factors affecting outcome in ocular myasthenia gravis.
Mazzoli M, Ariatti A, Valzania F, Kaleci S, Tondelli M, Nichelli PF, Galassi G. Mazzoli M, et al. Among authors: galassi g. Int J Neurosci. 2018 Jan;128(1):15-24. doi: 10.1080/00207454.2017.1344237. Epub 2017 Jul 17. Int J Neurosci. 2018. PMID: 28625092
A heroin addict with focal weakness.
Galassi G, Ariatti A, Gozzi M, Cavazza S. Galassi G, et al. Acta Myol. 2013 May;32(1):27-9. Acta Myol. 2013. PMID: 23853507 Free PMC article.
Early imaging in paraparetic Guillain-Barré syndrome.
Galassi G, Genovese M, Ariatti A, Malagoli M. Galassi G, et al. Acta Neurol Belg. 2020 Apr;120(2):453-454. doi: 10.1007/s13760-017-0854-z. Epub 2017 Oct 31. Acta Neurol Belg. 2020. PMID: 29086896 No abstract available.
197 results