Migraine headache: a review of the molecular genetics of a common disorder

Por Di Lorenzo, Cherubino, Grieco, Gaetano S., Santorelli, Filippo M.
Publicado em 2012

Molecular genotype in migraine

Por Di Lorenzo, Cherubino, Grieco, Gaetano S, Rubegni, Anna, Santorelli, Filippo M
Publicado no J Headache Pain (2015)

O041. GRIA3 (glutamate receptor, ionotropic, ampa 3) gene polymorphism influences cortical response to somatosensory stimulation in medication-overuse headache (MOH) patients

Por Di Lorenzo, Cherubino, Coppola, Gianluca, Grieco, Gaetano, Santorelli, Filippo Maria, Pascale, Esterina, Pierelli, Francesco
Publicado no J Headache Pain (2015)

Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management

Por Zucca, Susanna, Villaraggia, Margherita, Gagliardi, Stella, Grieco, Gaetano Salvatore, Valente, Marialuisa, Cereda, Cristina, Magni, Paolo
Publicado no BMC Bioinformatics (2016)

The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation Medicine

Por Pellacani, Simona, Sicca, Federico, Di Lorenzo, Cherubino, Grieco, Gaetano S., Valvo, Giulia, Cereda, Cristina, Rubegni, Anna, Santorelli, Filippo M.
Publicado no Front Cell Neurosci (2016)

Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism

Por Di Lorenzo, Cherubino, Di Lorenzo, Giorgio, Sances, Grazia, Ghiotto, Natascia, Guaschino, Elena, Grieco, Gaetano S., Santorelli, Filippo M., Casali, Carlo, Troisi, Alfonso, Siracusano, Alberto, Pierelli, Francesco
Publicado em 2009

Novel CLN3 mutation causing autophagic vacuolar myopathy

Por Cortese, Andrea, Tucci, Arianna, Piccolo, Giovanni, Galimberti, Carlo A., Fratta, Pietro, Marchioni, Enrico, Grampa, Gianpiero, Cereda, Cristina, Grieco, Gaetano, Ricca, Ivana, Pittman, Alan, Ciscato, Patrizia, Napoli, Laura, Lucchini, Valeria, Ripolone, Michela, Violano, Raffaella, Fagiolari, Gigliola, Mole, Sara E., Hardy, John, Moglia, Arrigo, Moggio, Maurizio
Publicado em 2014

Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy

Por Bello, Luca, Piva, Luisa, Barp, Andrea, Taglia, Antonella, Picillo, Esther, Vasco, Gessica, Pane, Marika, Previtali, Stefano C., Torrente, Yvan, Gazzerro, Elisabetta, Chiara Motta, Maria, Grieco, Gaetano S., Napolitano, Sara, Magri, Francesca, D'Amico, Adele, Astrea, Guja, Messina, Sonia, Sframeli, Maria, Luca Vita, Gian, Boffi, Patrizia, Mongini, Tiziana, Ferlini, Alessandra, Gualandi, Francesca, Soraru', Gianni, Ermani, Mario, Vita, Giuseppe, Battini, Roberta, Bertini, Enrico, Comi, Giacomo P., Berardinelli, Angela, Minetti, Carlo, Bruno, Claudio, Mercuri, Eugenio, Politano, Luisa, Angelini, Corrado, Hoffman, Eric P., Pegoraro, Elena
Publicado em 2012