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Page 1
GSK3β genetic variability in patients with Multiple Sclerosis.
Galimberti D, Macmurray J, Scalabrini D, Fenoglio C, De Riz M, Comi C, Comings D, Cortini F, Villa C, Serpente M, Cantoni C, Ridolfi E, Fardipoor MH, Leone M, Monaco F, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: ridolfi e. Neurosci Lett. 2011 Jun 15;497(1):46-8. doi: 10.1016/j.neulet.2011.04.024. Epub 2011 Apr 17. Neurosci Lett. 2011. PMID: 21527318
Dosage-dependent copy number gains in E2f1 and E2f3 drive hepatocellular carcinoma.
Kent LN, Bae S, Tsai SY, Tang X, Srivastava A, Koivisto C, Martin CK, Ridolfi E, Miller GC, Zorko SM, Plevris E, Hadjiyannis Y, Perez M, Nolan E, Kladney R, Westendorp B, de Bruin A, Fernandez S, Rosol TJ, Pohar KS, Pipas JM, Leone G. Kent LN, et al. Among authors: ridolfi e. J Clin Invest. 2017 Mar 1;127(3):830-842. doi: 10.1172/JCI87583. Epub 2017 Jan 30. J Clin Invest. 2017. PMID: 28134624 Free PMC article.
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia.
Galimberti D, Dell'Osso B, Fenoglio C, Villa C, Cortini F, Serpente M, Kittel-Schneider S, Weigl J, Neuner M, Volkert J, Leonhard C, Olmes DG, Kopf J, Cantoni C, Ridolfi E, Palazzo C, Ghezzi L, Bresolin N, Altamura AC, Scarpini E, Reif A. Galimberti D, et al. Among authors: ridolfi e. PLoS One. 2012;7(4):e32164. doi: 10.1371/journal.pone.0032164. Epub 2012 Apr 10. PLoS One. 2012. PMID: 22505994 Free PMC article.
Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis.
Ridolfi E, Fenoglio C, Cantoni C, Calvi A, De Riz M, Pietroboni A, Villa C, Serpente M, Bonsi R, Vercellino M, Cavalla P, Galimberti D, Scarpini E. Ridolfi E, et al. Int J Mol Sci. 2013 Feb 25;14(3):4375-84. doi: 10.3390/ijms14034375. Int J Mol Sci. 2013. PMID: 23439547 Free PMC article.
C9ORF72 repeat expansion not detected in patients with multiple sclerosis.
Fenoglio C, De Riz M, Villa C, Serpente M, Ridolfi E, Bonsi R, Cioffi SM, Barone C, Pietroboni A, Calvi A, Scarpini E, Galimberti D. Fenoglio C, et al. Among authors: ridolfi e. Neurobiol Aging. 2014 May;35(5):1213.e1-2. doi: 10.1016/j.neurobiolaging.2013.10.096. Epub 2013 Nov 1. Neurobiol Aging. 2014. PMID: 24355526
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
Villa C, Ghezzi L, Pietroboni AM, Fenoglio C, Cortini F, Serpente M, Cantoni C, Ridolfi E, Marcone A, Benussi L, Ghidoni R, Jacini F, Arighi A, Fumagalli GG, Mandelli A, Binetti G, Cappa S, Bresolin N, Scarpini E, Galimberti D. Villa C, et al. Among authors: ridolfi e. J Alzheimers Dis. 2011;26(1):19-26. doi: 10.3233/JAD-2011-102124. J Alzheimers Dis. 2011. PMID: 21558644
20 results