DI MARIA, EMILIO

DI MARIA, EMILIO  

100011 - Dipartimento di Scienze della salute  

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Titolo Data di pubblicazione Autore(i) File
"The true native chromatin- DNA stucture and cell cycle" 1-gen-1988 Vergani, Laura; Diaspro, ALBERTO GIOVANNI; DI MARIA, Emilio; I., Grasso; A., Pastorino; Nicolini, Claudio
"Thermodynamic characterization of chromatin stuctural alterations related to cell cycle progression" 1-gen-1987 Vergani, Laura; Diaspro, ALBERTO GIOVANNI; G., Cittadini; DI MARIA, Emilio; Nicolini, Claudio
19q13 microdeletion syndrome: Further refining the critical region 1-gen-2012 F., Forzano; F., Napoli; V., Uliana; M., Malacarne; C., Viaggi; R., Bloise; Coviello, Domenico; DI MARIA, Emilio; I., Olivieri; DI IORGI, Natascia; F., Faravelli
3q26.33–3q27.2 microdeletion: A new microdeletion syndrome? 1-gen-2013 Giorgia, Mandrile; Anna, Dubois; Jodi D., Hoffman; Vera, Uliana; DI MARIA, Emilio; Michela, Malacarne; Domenico, Coviello; Francesca, Faravelli; Simon, Zwolinski; Stephen, Hellens; Michael, Wright; Francesca, Forzano
A case study of a ’policy network’ for the promotion of migrant health: the Italian Society of Migration Medicine (SIMM) 1-gen-2018 Marceca, Maurizio; Bodini, Chiara; Bonciani, Manila; Di Maria, Emilio; Forcella, Emanuela; Mazzetti, Marco; Mondo, Luisa; Rinaldi, Alessandro; Russo, Maria Laura
A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci. 1-gen-2002 Bellone, Emilia; Rodolico, C.; Toscano, A.; DI MARIA, Emilio; Cassandrini, D.; Pizzuti, A.; Pigullo, S.; Mazzeo, A.; Macaione, V.; Girlanda, P.; Vita, G.; Ajmar, Franco; Mandich, Paola
A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference. 1-gen-2009 Lombardi, Ms; Jaspers, L; Spronkmans, C; Gellera, C; Taroni, F; DI MARIA, Emilio; DI DONATO, S; Kaemmerer, W.
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length 1-gen-2004 Brinkman, R. R.; Falush, D.; Paulsen, J. S.; Hayden, M. R.; ON BEHALF OF AN INTERNATIONAL HUNTINGTON'S DISEASE COLLABORATIVE, Group; DI MARIA, Emilio
A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease. 1-gen-1999 Bellone, Emilia; DI MARIA, Emilio; Soriani, S; Varese, A; Doria, Ll; Ajmar, Franco; Mandich, Paola
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect 1-gen-2004 DI MARIA, Emilio; Gulli, R.; Balestra, P.; Cassandrini, D.; Pigullo, S.; DORIA LAMBA, L.; Bado, M.; Schenone, Angelo; Ajmar, Franco; Mandich, Paola; Bellone, Emilia
A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease 1-gen-2004 Santoro, L.; Manganelli, F.; DI MARIA, Emilio; Bordo, D.; Cassandrini, D.; Ajmar, Franco; Mandich, Paola; Bellone, Emilia
A patient with a skull defect, dysmorphic features, hypopituitarism, and abnormal cortical development. 1-gen-2011 Accorsi, P; Giordano, L; Uliana, V; Forzano, F; Pinelli, L; Olioso, G; Zenker, M; DI MARIA, Emilio; Faravelli, F.
A putative regulatory subunit (NR3A) of the NMDA receptor complex as candidate gene for susceptibility to schizophrenia: a case-control study 1-gen-2007 Gulli, R; Masnata, B; Bonvicini, C; Tura, Gb; Manglaviti, L; Vaggi, M; Mollica, M; Bellone, Emilia; Mandich, Paola; Gennarelli, M; DI MARIA, Emilio
A single nucleotide variant in the FMR1 CGG repeat results in a "pseudodeletion" and is not associated with the fragile X syndrome phenotype 1-gen-2008 Cecconi, M; Forzano, F; Rinaldi, R; Cappellacci, S; Grammatico, P; Faravelli, F; DAGNA BRICARELLI, F; DI MARIA, Emilio; Grasso, M.
A sud del Mediterraneo – L’accoglienza oltre i confini del mare. Atti dell’inaugurazione del Corso di Ateneo in Cooperazione Internazionale allo sviluppo 2018/19 1-gen-2019 DI MARIA, Emilio
Adoption of Guidelines concerning medical examinations on arrival for asylum seekers and refugees: systematic review of literature and proposals for an implementation plan in Italy 1-gen-2018 Di Maria, Emilio; Roveta, Sara
An abnormal mRNA produced by a novel PMP22 splice site mutation associated with HNPP 1-gen-2006 Bellone, Emilia; Balestra, P; Ribizzi, G; Schenone, Angelo; Zocchi, G; DI MARIA, Emilio; Ajmar, Franco; Mandich, Paola
An open letter for the people in Gaza 1-gen-2014 Manduca, Paola; Chalmers, Iain; Summerfield, Derek; Gilbert, Mads; Ang, Swee; Hay, Alastar; Rose, Steven; Rose, Hilary; Stefanini, Angelo; Balduzzi, Andrea; Cigliano, Bruno; Pecoraro, Carmine; DI MARIA, Emilio; Camandona, Franco; Veronese, Guido; Ramenghi, Luca; Rui, Marina; Del Carlo, Pierina; D'Agostino, Sergio; Russo, Silvana; Luisi, Vincenzo; Papa, Stefania; Agnoletto, Vittorio; Agnoletto, Mariagiulia
Application of Genetics in the Elderly: Development, Integration, Analyses - AGE-DIAmond: development of a model based on clinical and genetic determinants to predict clinical outcome 1-gen-2017 Briata, IRENE MARIA; Prete, Camilla; Senesi, Barbara; Veneziano, Massimo; Sacchi, Nicoletta; Gennarelli, Massimo; Pilotto, Alberto; DI MARIA, Emilio
Arthropathy, Osteolysis, Keloids, Relapsing Conjunctival Pannus and Gingival Overgrowth: A Variant of Polyfibromatosis? 1-gen-2013 Cinotti, E1; Ferrero, G; Paparo, F; Papadia, M; Faravelli, F; Rongioletti, F; Traverso, C; Di Maria, E.