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Encomium: Giovanni Neri--polyhedral and down-to-earth mentor
2013 Genuardi, Maurizio; Gurrieri, Fiorella; Zollino, Marcella
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype
2013 Cordelli, Dm; Garavelli, L; Savasta, S; Guerra, A; Pellicciari, A; Giordano, L; Bonetti, S; Cecconi, I; Wischmeijer, A; Seri, M; Rosato, S; Gelmini, C; Della Giustina, E; Ferrari, Ar; Zanotta, N; Epifanio, R; Grioni, D; Malbora, B; Mammi, I; Mari, F; Buoni, S; Mostardini, R; Grosso, S; Pantaleoni, C; Doz, M; Poch Olivé, Ml; Rivieri, F; Sorge, G; Simonte, G; Licata, F; Tarani, L; Terazzi, E; Mazzanti, L; Cerruti Mainardi, P; Boni, A; Faravelli, F; Grasso, M; Bianchi, P; Zollino, Marcella; Franzoni, E.
Epilepsy in ring 14 syndrome: a clinical and EEG study of 22 patients
2013 Giovannini, Silvia; Marangio, L; Fusco, C; Scarano, A; Frattini, D; Della Giustina, E; Zollino, Marcella; Neri, Giovanni; Gobbi, G.
Evidence for a founder effect of the MPL-S505N mutation in eight Italian pedigrees with hereditary thrombocythemia
2009 Liu, K; Martini, Maurizio; Rocca, Bianca; Amos, Ci; Teofili, Luciana; Giona, F; Ding, J; Komatsu, H; Larocca, Luigi Maria; Skoda, Rc
Fibroblast growth factor 23 serum level in type 2 diabetic italian subjects with peripheral arterial disease and critical limb ischemia.
2016 Biscetti, Federico; Straface, Giuseppe; Pitocco, Dario; Angelini, Flavia; Tinelli, Giovanni; Landolfi, Raffaele; Flex, Andrea
Focal dermal hypoplasia (goltz-gorlin syndrome): A new case with a novel variant in the PORCN gene (c.1250T > C:p.F417S) and unusual spinal anomaly
2013 Garavelli, L; Simonte, G; Rosato, S; Wischmeijer, A; Albertini, E; Guareschi, E; Longo, C; Albertini, G; Gelmini, C; Greco, C; Errico, S; Pavanello, M; Happle, R; Unger, S; Superti Furga, A; Grzeschik, K; Savino, Gustavo
Formoterol-induced downregulation of the beta2-adrenoceptor in asthmatics with homozygous glycine-16 polymorphism
2013 Fuso, Leonello; Di Perna, Alessandra; Longobardi, Anna; Trove', Andrea; Bisceglia, Michela; Bibi, Benedetta; Angelozzi, Carla; Tiziano, Francesco Danilo; Antonelli Incalzi, Raffaele
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder
2009 Gurrieri, Fiorella; Neri, Giovanni; Boccuto, Luigi
Gene expression profiling of pancreas neuroendocrine tumors with different ki67‐based grades
2021 Simbolo, M.; Bilotta, M.; Mafficini, A.; Luchini, C.; Furlan, D.; Inzani, F.; Petrone, G.; Bonvissuto, D.; Rosa, S. L.; Schinzari, G.; Bianchi, A.; Rossi, E.; Menghi, R.; Giuliante, F.; Boccia, S.; Scarpa, A.; Rindi, G.
-Genetic analysis of the dystroglycan gene in brochopulmnary dysplasia affected premature newbors
2007 Concolino, P.; Capoluongo, E.; Santonocito, E.; Vento, Giovanni; Tana, Milena; Romagnoli, Costantino; Zuppi, Cecilia; Ameglio, F.; Brancaccio, A.; Sciandra, F.
Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges
2014 Marangi, Giuseppe; Traynor, Bj
Genetic counselling in ALS: facts, uncertainties and clinical suggestions
2013 Chiò, A; Battistini, S; Calvo, A; Caponnetto, C; Conforti, Fl; Corbo, M; Giannini, F; Mandrioli, J; Mora, G; Sabatelli, Mario; Ajmone, C; Mastro, E; Pain, D; Mandich, P; Penco, S; Restagno, G; Zollino, Marcella; Surbone, A.
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
2010 Pola, Roberto; Gaetani, Eleonora
A Genome-wide Association Study of Myasthenia Gravis
2015 Renton, Ae; Pliner, Ha; Provenzano, Carlo; Evoli, Amelia; Ricciardi, R; Nalls, Ma; Marangi, Giuseppe; Abramzon, Y; Arepalli, S; Chong, S; Hernandez, Dg; Johnson, Jo; Bartoccioni, Emanuela; Scuderi, Flavia; Maestri, M; Gibbs, Jr; Errichiello, E; Chiò, A; Restagno, G; Sabatelli, Mario; Macek, M; Scholz, Sw; Corse, A; Chaudhry, V; Benatar, M; Barohn, Rj; Mcvey, A; Pasnoor, M; Dimachkie, Mm; Rowin, J; Kissel, J; Freimer, M; Kaminski, Hj; Sanders, Db; Lipscomb, B; Massey, Jm; Chopra, M; Howard, Jf; Koopman, Wj; Nicolle, Mw; Pascuzzi, Rm; Pestronk, A; Wulf, C; Florence, J; Blackmore, D; Soloway, A; Siddiqi, Z; Muppidi, S; Wolfe, G; Richman, D; Mezei, Mm; Jiwa, T; Oger, J; Drachman, Db; Traynor, Bj
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.
2011 Boccia, Stefania; Inhance, Consortium
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome.
2009 Neri, Giovanni
Geographic heterogeneity in the prevalence of human papillomavirus in head and neck cancer
2017 Anantharaman, Devasena; Abedi Ardekani, Behnoush; Beachler, Daniel C; Gheit, Tarik; Olshan, Andrew F; Wisniewski, Kathy; Wunsch Filho, Victor; Toporcov, Tatiana N; Tajara, Eloiza H; Levi, José Eduardo; Moyses, Raquel A; Boccia, Stefania; Cadoni, Gabriella; Rindi, Guido; Ahrens, Wolfgang; Merletti, Franco; Conway, David I; Wright, Sylvia; Carreira, Christine; Renard, Helene; Chopard, Priscilia; McKay Chopin, Sandrine; Scelo, Ghislaine; Tommasino, Massimo; Brennan, Paul; D'Souza, Gypsyamber
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin.
2008 Hennies, Hc; Kornak, U; Zhang, H; Egerer, J; Zhang, X; Seifert, W; Kuhnisch, J; Budde, B; Natebus, M; Brancati, F; Wilcox, Wr; Muller, D; Kaplan, Pb; Rajab, A; Zampino, Giuseppe; Fodale, V; Dallapiccola, B; Newman, W; Metcalfe, K; Clayton Smith, J; Tassabehji, M; Steinmann, B; Barr, Fa; Nurnberg, P; Wieacker, P; Mundlos, S.
Glucokinase regulatory protein gene polymorphism affects liver fibrosis in non-alcoholic fatty liver disease
2014 Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A.
Glucokinase Regulatory Protein Gene Polymorphism Affects Liver Fibrosis in Non-Alcoholic Fatty Liver Disease
2014 Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A.
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2013 | Encomium: Giovanni Neri--polyhedral and down-to-earth mentor | Genuardi, Maurizio; Gurrieri, Fiorella; Zollino, Marcella | |
1-gen-2013 | Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype | Cordelli, Dm; Garavelli, L; Savasta, S; Guerra, A; Pellicciari, A; Giordano, L; Bonetti, S; Cecconi, I; Wischmeijer, A; Seri, M; Rosato, S; Gelmini, C; Della Giustina, E; Ferrari, Ar; Zanotta, N; Epifanio, R; Grioni, D; Malbora, B; Mammi, I; Mari, F; Buoni, S; Mostardini, R; Grosso, S; Pantaleoni, C; Doz, M; Poch Olivé, Ml; Rivieri, F; Sorge, G; Simonte, G; Licata, F; Tarani, L; Terazzi, E; Mazzanti, L; Cerruti Mainardi, P; Boni, A; Faravelli, F; Grasso, M; Bianchi, P; Zollino, Marcella; Franzoni, E. | |
1-gen-2013 | Epilepsy in ring 14 syndrome: a clinical and EEG study of 22 patients | Giovannini, Silvia; Marangio, L; Fusco, C; Scarano, A; Frattini, D; Della Giustina, E; Zollino, Marcella; Neri, Giovanni; Gobbi, G. | |
1-gen-2009 | Evidence for a founder effect of the MPL-S505N mutation in eight Italian pedigrees with hereditary thrombocythemia | Liu, K; Martini, Maurizio; Rocca, Bianca; Amos, Ci; Teofili, Luciana; Giona, F; Ding, J; Komatsu, H; Larocca, Luigi Maria; Skoda, Rc | |
1-gen-2016 | Fibroblast growth factor 23 serum level in type 2 diabetic italian subjects with peripheral arterial disease and critical limb ischemia. | Biscetti, Federico; Straface, Giuseppe; Pitocco, Dario; Angelini, Flavia; Tinelli, Giovanni; Landolfi, Raffaele; Flex, Andrea | |
1-gen-2013 | Focal dermal hypoplasia (goltz-gorlin syndrome): A new case with a novel variant in the PORCN gene (c.1250T > C:p.F417S) and unusual spinal anomaly | Garavelli, L; Simonte, G; Rosato, S; Wischmeijer, A; Albertini, E; Guareschi, E; Longo, C; Albertini, G; Gelmini, C; Greco, C; Errico, S; Pavanello, M; Happle, R; Unger, S; Superti Furga, A; Grzeschik, K; Savino, Gustavo | |
1-gen-2013 | Formoterol-induced downregulation of the beta2-adrenoceptor in asthmatics with homozygous glycine-16 polymorphism | Fuso, Leonello; Di Perna, Alessandra; Longobardi, Anna; Trove', Andrea; Bisceglia, Michela; Bibi, Benedetta; Angelozzi, Carla; Tiziano, Francesco Danilo; Antonelli Incalzi, Raffaele | |
1-gen-2009 | Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder | Gurrieri, Fiorella; Neri, Giovanni; Boccuto, Luigi | |
1-gen-2021 | Gene expression profiling of pancreas neuroendocrine tumors with different ki67‐based grades | Simbolo, M.; Bilotta, M.; Mafficini, A.; Luchini, C.; Furlan, D.; Inzani, F.; Petrone, G.; Bonvissuto, D.; Rosa, S. L.; Schinzari, G.; Bianchi, A.; Rossi, E.; Menghi, R.; Giuliante, F.; Boccia, S.; Scarpa, A.; Rindi, G. | |
1-gen-2007 | -Genetic analysis of the dystroglycan gene in brochopulmnary dysplasia affected premature newbors | Concolino, P.; Capoluongo, E.; Santonocito, E.; Vento, Giovanni; Tana, Milena; Romagnoli, Costantino; Zuppi, Cecilia; Ameglio, F.; Brancaccio, A.; Sciandra, F. | |
1-gen-2014 | Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges | Marangi, Giuseppe; Traynor, Bj | |
1-gen-2013 | Genetic counselling in ALS: facts, uncertainties and clinical suggestions | Chiò, A; Battistini, S; Calvo, A; Caponnetto, C; Conforti, Fl; Corbo, M; Giannini, F; Mandrioli, J; Mora, G; Sabatelli, Mario; Ajmone, C; Mastro, E; Pain, D; Mandich, P; Penco, S; Restagno, G; Zollino, Marcella; Surbone, A. | |
1-gen-2010 | Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm | Pola, Roberto; Gaetani, Eleonora | |
1-gen-2015 | A Genome-wide Association Study of Myasthenia Gravis | Renton, Ae; Pliner, Ha; Provenzano, Carlo; Evoli, Amelia; Ricciardi, R; Nalls, Ma; Marangi, Giuseppe; Abramzon, Y; Arepalli, S; Chong, S; Hernandez, Dg; Johnson, Jo; Bartoccioni, Emanuela; Scuderi, Flavia; Maestri, M; Gibbs, Jr; Errichiello, E; Chiò, A; Restagno, G; Sabatelli, Mario; Macek, M; Scholz, Sw; Corse, A; Chaudhry, V; Benatar, M; Barohn, Rj; Mcvey, A; Pasnoor, M; Dimachkie, Mm; Rowin, J; Kissel, J; Freimer, M; Kaminski, Hj; Sanders, Db; Lipscomb, B; Massey, Jm; Chopra, M; Howard, Jf; Koopman, Wj; Nicolle, Mw; Pascuzzi, Rm; Pestronk, A; Wulf, C; Florence, J; Blackmore, D; Soloway, A; Siddiqi, Z; Muppidi, S; Wolfe, G; Richman, D; Mezei, Mm; Jiwa, T; Oger, J; Drachman, Db; Traynor, Bj | |
1-gen-2011 | A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. | Boccia, Stefania; Inhance, Consortium | |
1-gen-2009 | Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome. | Neri, Giovanni | |
1-gen-2017 | Geographic heterogeneity in the prevalence of human papillomavirus in head and neck cancer | Anantharaman, Devasena; Abedi Ardekani, Behnoush; Beachler, Daniel C; Gheit, Tarik; Olshan, Andrew F; Wisniewski, Kathy; Wunsch Filho, Victor; Toporcov, Tatiana N; Tajara, Eloiza H; Levi, José Eduardo; Moyses, Raquel A; Boccia, Stefania; Cadoni, Gabriella; Rindi, Guido; Ahrens, Wolfgang; Merletti, Franco; Conway, David I; Wright, Sylvia; Carreira, Christine; Renard, Helene; Chopard, Priscilia; McKay Chopin, Sandrine; Scelo, Ghislaine; Tommasino, Massimo; Brennan, Paul; D'Souza, Gypsyamber | |
1-gen-2008 | Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin. | Hennies, Hc; Kornak, U; Zhang, H; Egerer, J; Zhang, X; Seifert, W; Kuhnisch, J; Budde, B; Natebus, M; Brancati, F; Wilcox, Wr; Muller, D; Kaplan, Pb; Rajab, A; Zampino, Giuseppe; Fodale, V; Dallapiccola, B; Newman, W; Metcalfe, K; Clayton Smith, J; Tassabehji, M; Steinmann, B; Barr, Fa; Nurnberg, P; Wieacker, P; Mundlos, S. | |
1-gen-2014 | Glucokinase regulatory protein gene polymorphism affects liver fibrosis in non-alcoholic fatty liver disease | Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A. | |
1-gen-2014 | Glucokinase Regulatory Protein Gene Polymorphism Affects Liver Fibrosis in Non-Alcoholic Fatty Liver Disease | Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A. |
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