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A gene expression phenotype in lymphocytes from Friedreich ataxia patients.
Coppola G, Burnett R, Perlman S, Versano R, Gao F, Plasterer H, Rai M, Saccá F, Filla A, Lynch DR, Rusche JR, Gottesfeld JM, Pandolfo M, Geschwind DH. Coppola G, et al. Among authors: geschwind dh. Ann Neurol. 2011 Nov;70(5):790-804. doi: 10.1002/ana.22526. Ann Neurol. 2011. PMID: 22162061 Free PMC article.
Genomic profiles of damage and protection in human intracerebral hemorrhage.
Carmichael ST, Vespa PM, Saver JL, Coppola G, Geschwind DH, Starkman S, Miller CM, Kidwell CS, Liebeskind DS, Martin NA. Carmichael ST, et al. Among authors: geschwind dh. J Cereb Blood Flow Metab. 2008 Nov;28(11):1860-75. doi: 10.1038/jcbfm.2008.77. Epub 2008 Jul 16. J Cereb Blood Flow Metab. 2008. PMID: 18628781 Free PMC article.
Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study.
Criscuolo C, Filla A, Coppola G, Rinaldi C, Carbone R, Pinto S, Wang Q, de Leva MF, Salvatore E, Banfi S, Brunetti A, Quarantelli M, Geschwind DH, Pappatà S, De Michele G. Criscuolo C, et al. Among authors: geschwind dh. J Neurol. 2009 Aug;256(8):1252-7. doi: 10.1007/s00415-009-5109-3. Epub 2009 Apr 12. J Neurol. 2009. PMID: 19363635
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARgamma pathway as a therapeutic target in Friedreich's ataxia.
Coppola G, Marmolino D, Lu D, Wang Q, Cnop M, Rai M, Acquaviva F, Cocozza S, Pandolfo M, Geschwind DH. Coppola G, et al. Among authors: geschwind dh. Hum Mol Genet. 2009 Jul 1;18(13):2452-61. doi: 10.1093/hmg/ddp183. Epub 2009 Apr 17. Hum Mol Genet. 2009. PMID: 19376812 Free PMC article.
587 results