NOVELLI, GIUSEPPE

NOVELLI, GIUSEPPE  

Dipartimento di Biomedicina e prevenzione  

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Risultati 1 - 20 di 457 (tempo di esecuzione: 0.034 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1995 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot Amati, F; Mari, A; Digilio, Mc; Mingarelli, R; Marino, B; Giannotti, A; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-2002 3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population Vavassori, P; Borgiani, P; D'Apice, Mr; De Negris, F; DEL VECCHIO BLANCO, G; Monteleone, I; Biancone, L; Novelli, G; Pallone, E Articolo su rivista
1-gen-1998 A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-2006 A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice Cipollone, D; Amati, F; Carsetti, R; Placidi, S; Biancolella, M; D'Amati, G; Novelli, G; Siracusa, G; Marino, B Articolo su rivista
1-gen-2013 ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique Ciccacci, C; Di Fusco, D; Marazzi, M; Liotta, G; Palombi, L; Novelli, G; Borgiani, P Articolo su rivista
1-gen-2012 Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues Rinaldi, F; Terracciano, C; Pisani, V; Massa, R; Loro, E; Vergani, L; DI GIROLAMO, S; Angelini, C; Gourdon, G; Novelli, G; Botta, A Articolo su rivista
1-lug-2000 Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women Semprini, S; Mango, R; Brancati, F; Dallapiccola, B; Becherini, L; Novelli, G; DE LORENZO, A; Brandi, M; Gennari, L Articolo su rivista
1-gen-2014 Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis Terrinoni, A; Giardina, E; Pertusi, G; Cascella, R; Serra, V; Bornacina, C; Palombo, R; Tiberio, R; Gattoni, M; Novelli, G; Annicchiarico Petruzzelli, M; Melino, G; Colombo, E Articolo su rivista
1-gen-2016 Advances in exploring the role of micrornas in inflammatory bowel disease Ciccacci, C; Politi, C; Novelli, G; Borgiani, P Articolo su rivista
1-gen-1995 Advances in molecular analysis of congenital heart defects Dallapiccola, B; Amati, F; Gennarelli, M; Mari, A; Novelli, G Articolo su rivista
1-gen-2018 AFM nano-mechanical study of the beating profile of hiPSC-derived cardiomyocytes beating bodies WT and DM1 Dinarelli, S; Girasole, M; Spitalieri, P; Talarico, Rv; Murdocca, M; Botta, A; Novelli, G; Mango, R; Sangiuolo, F; Longo, G Articolo su rivista
1-set-2010 Age-period-cohort analysis of 1990-2003 incidence time trends of childhood diabetes in Italy: the RIDI study Bruno, G; Maule, M; Merletti, F; Novelli, G; Falorni, A; Iannilli, A; Iughetti, L; Altobelli, E; D'Annunzio, G; Piffer, S; Pozzilli, P; Iafusco, D; Songini, M; Roncarolo, F; Toni, S; Carle, F; Cherubini, V Articolo su rivista
1-gen-2014 Age-related macular degeneration: insights into inflammatory genes Cascella, R; Ragazzo, M; Strafella, C; Missiroli, F; Borgiani, P; Angelucci, F; Marsella, Lt; Cusumano, A; Novelli, G; Ricci, F; Giardina, E Articolo su rivista
1-feb-2016 An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy Vanacore, N; Rastelli, E; Antonini, G; Bianchi, M; Botta, A; Bucci, E; Casali, C; Costanzi Porrini, S; Giacanelli, M; Gibellini, M; Modoni, A; Novelli, G; Pennisi, E; Petrucci, A; Piantadosi, C; Silvestri, G; Terracciano, C; Massa, R Articolo su rivista
1-gen-2008 Ala197Thr is not associated with susceptibility to Crohn’s Disease or with phenotype in an Italian population. Perricone, C; Borgiani, P; Romano, S; Ciccacci, C; Fusco, G; Novelli, G; Biancone, L; Calabrese, E; Pallone, F Articolo su rivista
1-gen-2007 Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians Borgiani, P; Ciccacci, C; Forte, V; Romano, S; Federici, G; Novelli, G Articolo su rivista
1-gen-2021 Altered expression of miR-142, miR-155, miR-499a and of their putative common target MDM2 in systemic lupus erythematosus Latini, A; Ciccacci, C; De Benedittis, G; Novelli, L; Ceccarelli, F; Conti, F; Novelli, G; Perricone, C; Borgiani, P Articolo su rivista
1-gen-2005 Altered pre-lamin A processing is a common mechanism leading to lipodystrophy Capanni, C; Mattioli, E; Columbaro, M; Lucarelli, E; Parnaik, V; Novelli, G; Wehnert, M; Cenni, V; Maraldi, N; Squarzoni, S; Lattanzi, G Articolo su rivista
1-ott-1991 Analysis of 14 cystic fibrosis mutations in five south European populations Nunes, V; Gasparini, P; Novelli, G; Gaona, A; Bonizzato, A; Sangiuolo, Fc; Balassopoulou, A; Giménez, F; Dognini, M; Ravnik Glavac, M Articolo su rivista
1-gen-2020 Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications Strafella, C; Caputo, V; Termine, A; Barati, S; Gambardella, S; Borgiani, P; Caltagirone, C; Novelli, G; Giardina, E; Cascella, R Articolo su rivista