RICCIO, Andrea

RICCIO, Andrea  

Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche (DISTABiF)  

Mostra records
Risultati 1 - 20 di 111 (tempo di esecuzione: 0.025 secondi).
Titolo Data di pubblicazione Autore(i) File
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 1-gen-2011 Garavelli, L; Rosato, S; Wischmeijer, A; Gelmini, C; Esposito, A; Mazzanti, L; Franchi, F; De Crescenzo, A; Palumbo, O; Carella, M; Riccio, Andrea
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 1-gen-2010 Zollino, M; Orteschi, D; Marangi, G; De Crescenzo, A; Pecile, V; Riccio, Andrea; Neri, G.
A common response element mediates differential effects of phorbol esters and forskolin on type‐1 plasminogen activator inhibitor gene expression in human breast carcinoma cells 1-gen-1994 Knudsen, H; Olesen, T; Riccio, Andrea; Ungaro, P; Christensen, L; Andreasen, Pa
A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: A twelve-year follow-up and literature review 1-gen-2015 Stagi, Stefano; Lapi, Elisabetta; Pantaleo, Marilena; Carella, Massimo; Petracca, Antonio; De Crescenzo, Agostina; Zelante, Leopoldo; Riccio, Andrea; de Martino, Maurizio
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 1-gen-2015 Fryssira, Helen; Amenta, Stella; Kanber, Deniz; Sofocleous, Christalena; Lykopoulou, Evangelia; Kanaka Gantenbein, Christina; Cerrato, Flavia; Lüdecke, Hermann Josef; Bens, Susanne; Riccio, Andrea; Buiting, Karin
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 1-gen-2011 De Crescenzo, A; Coppola, F; Falco, P; Bernardo, I; Ausanio, G; Cerrato, Flavia; Falco, L; Riccio, Andrea
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma 1-gen-1996 Nardone, G; Romano, Marco; Calabro, A; Pedone, Paolo Vincenzo; Desio, I; Persico, M; Budillon, G; Bruni, Cb; Riccio, Andrea; Zarrilli, R.
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 1-gen-2017 Mussa, Alessandro; Molinatto, Cristina; Cerrato, Flavia; Palumbo, Orazio; Carella, Massimo; Baldassarre, Giuseppina; Carli, Diana; Peris, Clementina; Riccio, Andrea; Ferrero, Giovanni Battista
BamHI RFLP linked to the human urokinase gene 1-gen-1985 Sebastio, G; Riccio, Andrea; Verde, P; Scarpato, N; Blasi, F.
Beckwith-Wiedemann Syndrome 1-gen-2019 Mussa, A; Kalish, J; Cerrato, F; Riccio, A; Ferrero, Gb
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 1-gen-2018 Cammarata-Scalisi, Francisco; Avendaño, Andrea; Stock, Frances; Callea, Michele; Sparago, Angela; Riccio, Andrea
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 1-gen-2020 Fatemi, N.; Salehi, N.; Pignata, L.; Palumbo, P.; Cubellis, M. V.; Ramazanali, F.; Ray, P.; Varkiani, M.; Reyhani-Sabet, F.; Biglari, A.; Sparago, A.; Acurzio, B.; Palumbo, O.; Carella, M.; Riccio, A.; Totonchi, M.
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 1-gen-2020 Pignata, L.; Palumbo, O.; Cerrato, F.; Acurzio, B.; de Alava, E.; Roma, J.; Gallego, S.; Mora, J.; Carella, M.; Riccio, A.; Verde, G.
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol 1-gen-2016 Mussa, Alessandro; Molinatto, Cristina; Baldassarre, Giuseppina; Riberi, Evelise; Russo, Silvia; Larizza, Lidia; Riccio, Andrea; Ferrero, Giovanni Battista
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 1-gen-2016 Sanchez Delgado, Marta; Riccio, Andrea; Eggermann, Thomas; Maher, Eamonn R.; Lapunzina, Pablo; Mackay, Deborah; Monk, David
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 1-gen-2018 Brioude, Frédéric; Kalish, Jennifer M; Mussa, Alessandro; Foster, Alison C; Bliek, Jet; Ferrero, Giovanni Battista; Boonen, Susanne E; Cole, Trevor; Baker, Robert; Bertoletti, Monica; Cocchi, Guido; Coze, Carole; De Pellegrin, Maurizio; Hussain, Khalid; Ibrahim, Abdulla; Kilby, Mark D; Krajewska-Walasek, Malgorzata; Kratz, Christian P; Ladusans, Edmund J; Lapunzina, Pablo; Le Bouc, Yves; Maas, Saskia M; Macdonald, Fiona; Õunap, Katrin; Peruzzi, Licia; Rossignol, Sylvie; Russo, Silvia; Shipster, Caroleen; Skórka, Agata; Tatton-Brown, Katrina; Tenorio, Jair; Tortora, Chiara; Grønskov, Karen; Netchine, Irène; Hennekam, Raoul C; Prawitt, Dirk; Tümer, Zeynep; Eggermann, Thomas; Mackay, Deborah J. G; Riccio, Andrea; Maher, Eamonn R.
Clinical utility gene card for: Beckwith-Wiedemann Syndrome 1-gen-2014 Eggermann, T; Algar, E; Lapunzina, P; Mackay, D; Maher, E. R.; Mannens, M; Netchine, I; Prawitt, D; Riccio, Andrea; Temple, Ik; Weksberg, R.
Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care 1-gen-2015 Eggermann, Thomas; Netchine, Irène; Temple, Karen; Tümer, Zeynep; Monk, David; Mackay, Deborah; Grønskov, Karin; Riccio, Andrea; Linglart, Agnès; Maher, Eamonn R.
Convergently functional, Rho-independent terminator in Salmonella typhimurium 1-gen-1985 Carlomagno, Ms; Riccio, Andrea; Bruni, Cb
Developmentally regulated functions of the H19 differentially methylated domain 1-gen-2004 Vernucci, M.; Cerrato, Flavia; Pedone, Paolo Vincenzo; Dandolo, L.; Bruni, C. B.; Riccio, Andrea