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Page 1
Personalized therapy in a GRIN1 mutated girl with intellectual disability and epilepsy.
Papa FT, Mancardi MM, Frullanti E, Fallerini C, Della Chiara V, Zalba-Jadraque L, Baldassarri M, Gamucci A, Mari F, Veneselli E, Renieri A. Papa FT, et al. Among authors: gamucci a. Clin Dysmorphol. 2018 Jan;27(1):18-20. doi: 10.1097/MCD.0000000000000205. Clin Dysmorphol. 2018. PMID: 29194067 No abstract available.
Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2.
De Mori R, Severino M, Mancardi MM, Anello D, Tardivo S, Biagini T, Capra V, Casella A, Cereda C, Copeland BR, Gagliardi S, Gamucci A, Ginevrino M, Illi B, Lorefice E, Musaev D, Stanley V, Micalizzi A, Gleeson JG, Mazza T, Rossi A, Valente EM. De Mori R, et al. Among authors: gamucci a. Brain. 2019 Oct 1;142(10):2965-2978. doi: 10.1093/brain/awz247. Brain. 2019. PMID: 31412107 Free PMC article.
Intense gamma-ray source in the giant-dipole-resonance range driven by 10-TW laser pulses.
Giulietti A, Bourgeois N, Ceccotti T, Davoine X, Dobosz S, D'Oliveira P, Galimberti M, Galy J, Gamucci A, Giulietti D, Gizzi LA, Hamilton DJ, Lefebvre E, Labate L, Marquès JR, Monot P, Popescu H, Réau F, Sarri G, Tomassini P, Martin P. Giulietti A, et al. Among authors: gamucci a. Phys Rev Lett. 2008 Sep 5;101(10):105002. doi: 10.1103/PhysRevLett.101.105002. Epub 2008 Sep 3. Phys Rev Lett. 2008. PMID: 18851220