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Interleukin-1 cluster gene polymorphisms and aneurysmal subarachnoid hemorrhage.
Fontanella M, Rainero I, Gallone S, Rubino E, Fornaro R, Fenoglio P, Valfrè W, Vaula G, Benevello C, Ducati A, Pinessi L. Fontanella M, et al. Among authors: vaula g. Neurosurgery. 2010 Jun;66(6):1058-62; discussion 1062-3. doi: 10.1227/01.NEU.0000369187.95163.5D. Neurosurgery. 2010. PMID: 20495422
The 1246G-->A polymorphism of the HCRTR2 gene is not associated with migraine.
Pinessi L, Binello E, De Martino P, Gallone S, Gentile S, Rainero I, Rivoiro C, Rubino E, Savi L, Valfrè W, Vaula G. Pinessi L, et al. Among authors: vaula g. Cephalalgia. 2007 Aug;27(8):945-9. doi: 10.1111/j.1468-2982.2007.01347.x. Epub 2007 Jul 23. Cephalalgia. 2007. PMID: 17645762
Investigating the genetic role of aquaporin4 gene in migraine.
Rubino E, Rainero I, Vaula G, Crasto F, Gravante E, Negro E, Brega F, Gallone S, Pinessi L. Rubino E, et al. Among authors: vaula g. J Headache Pain. 2009 Apr;10(2):111-4. doi: 10.1007/s10194-009-0100-z. Epub 2009 Feb 10. J Headache Pain. 2009. PMID: 19209385 Free PMC article.
A new Italian pedigree with early-onset Alzheimer's disease.
Rainero I, Bergamini L, Bruni AC, Ferini-Strambi L, Foncin JF, Gei G, Macciardi F, Montesi MP, Pinessi L, Vaula G. Rainero I, et al. Among authors: vaula g. J Geriatr Psychiatry Neurol. 1994 Jan-Mar;7(1):28-32. J Geriatr Psychiatry Neurol. 1994. PMID: 8192827
Cluster headache attacks and multiple sclerosis.
Gentile S, Ferrero M, Vaula G, Rainero I, Pinessi L. Gentile S, et al. Among authors: vaula g. J Headache Pain. 2007 Sep;8(4):245-7. doi: 10.1007/s10194-007-0405-8. Epub 2007 Sep 24. J Headache Pain. 2007. PMID: 17901919 Free PMC article.
Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38).
Borroni B, Di Gregorio E, Orsi L, Vaula G, Costanzi C, Tempia F, Mitro N, Caruso D, Manes M, Pinessi L, Padovani A, Brusco A, Boccone L. Borroni B, et al. Among authors: vaula g. Parkinsonism Relat Disord. 2016 Jul;28:80-6. doi: 10.1016/j.parkreldis.2016.04.030. Epub 2016 Apr 27. Parkinsonism Relat Disord. 2016. PMID: 27143115 Free PMC article.
SOD1 missense mutation in an Italian family with ALS.
Rainero I, Pinessi L, Tsuda T, Vignocchi MG, Vaula G, Calvi L, Cerrato P, Rossi B, Bergamini L, McLachlan DR, et al. Rainero I, et al. Among authors: vaula g. Neurology. 1994 Feb;44(2):347-9. doi: 10.1212/wnl.44.2.347. Neurology. 1994. PMID: 8309590
57 results