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ELOVL5 mutations cause spinocerebellar ataxia 38.
Di Gregorio E, Borroni B, Giorgio E, Lacerenza D, Ferrero M, Lo Buono N, Ragusa N, Mancini C, Gaussen M, Calcia A, Mitro N, Hoxha E, Mura I, Coviello DA, Moon YA, Tesson C, Vaula G, Couarch P, Orsi L, Duregon E, Papotti MG, Deleuze JF, Imbert J, Costanzi C, Padovani A, Giunti P, Maillet-Vioud M, Durr A, Brice A, Tempia F, Funaro A, Boccone L, Caruso D, Stevanin G, Brusco A. Di Gregorio E, et al. Among authors: costanzi c. Am J Hum Genet. 2014 Aug 7;95(2):209-17. doi: 10.1016/j.ajhg.2014.07.001. Epub 2014 Jul 24. Am J Hum Genet. 2014. PMID: 25065913 Free PMC article.
Parkinson's disease and dementia.
Padovani A, Costanzi C, Gilberti N, Borroni B. Padovani A, et al. Among authors: costanzi c. Neurol Sci. 2006 Mar;27 Suppl 1:S40-3. doi: 10.1007/s10072-006-0546-6. Neurol Sci. 2006. PMID: 16708183 Review.
Role of BDNF Val66Met functional polymorphism in Alzheimer's disease-related depression.
Borroni B, Archetti S, Costanzi C, Grassi M, Ferrari M, Radeghieri A, Caimi L, Caltagirone C, Di Luca M, Padovani A; ITINAD Working Group. Borroni B, et al. Among authors: costanzi c. Neurobiol Aging. 2009 Sep;30(9):1406-12. doi: 10.1016/j.neurobiolaging.2007.11.023. Epub 2008 Jan 7. Neurobiol Aging. 2009. PMID: 18179845
51 results