Lettera e legge. Il problema dell'interpretazione e del confine tra potere legislativo e potere giudiziario
2022-01-01 Onorato, Michele
Gli accordi ristrutturazione finanziari ai sensi dell'art. 186 septies l. fall. Dalla rottura di una equazione al paradosso di un caso
2016-01-01 Onorato, Michele
Donazione di beni altrui e donazione del bene presente nell'asse ereditario indiviso
2006-01-01 Onorato, Michele
Accordi a sfavore di terzo? Profili dei negozi sulla crisi d'impresa
2022-01-01 Onorato, Michele
L'errore ostativo
2005-01-01 Onorato, Michele
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux
2021-01-01 Verbitsky, M; Krithivasan, P; Batourina, E; Khan, A; Graham, Se; Marasà, M; Kim, H; Lim, Ty; Weng, Pl; Sánchez-Rodríguez, E; Mitrotti, A; Ahram, Df; Zanoni, F; Fasel, Da; Westland, R; Sampson, Mg; Zhang, Jy; Bodria, M; Kil, Bh; Shril, S; Gesualdo, L; Torri, F; Scolari, F; Izzi, C; van Wijk, Jae; Saraga, M; Santoro, D; Conti, G; Barton, De; Dobson, Mg; Puri, P; Furth, Sl; Warady, Ba; Pisani, I; Fiaccadori, E; Allegri, L; Degl'Innocenti, Ml; Piaggio, G; Alam, S; Gigante, M; Zaza, G; Esposito, P; Lin, F; Simões-E-Silva, Ac; Brodkiewicz, A; Drozdz, D; Zachwieja, K; Miklaszewska, M; Szczepanska, M; Adamczyk, P; Tkaczyk, M; Tomczyk, D; Sikora, P; Mizerska-Wasiak, M; Krzemien, G; Szmigielska, A; Zaniew, M; Lozanovski, Vj; Gucev, Z; Ionita-Laza, I; Stanaway, Ib; Crosslin, Dr; Wong, Cs; Hildebrandt, F; Barasch, J; Kenny, Ee; Loos, Rjf; Levy, B; Ghiggeri, Gm; Hakonarson, H; Latos-Bieleńska, A; Materna-Kiryluk, A; Darlow, Jm; Tasic, V; Willer, C; Kiryluk, K; Sanna-Cherchi, S; Mendelsohn, Cl; Gharavi, Ag
Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome
2013-01-01 Handley, Mt; Morris-Rosendahl, Dj; Brown, S; Macdonald, F; Hardy, C; Bem, D; Carpanini, Sm; Borck, G; Martorell, L; Izzi, C; Faravelli, F; Accorsi, P; Pinelli, L; Basel-Vanagaite, L; Peretz, G; Abdel-Salam, Gm; Zaki, Ms; Jansen, A; Mowat, D; Glass, I; Stewart, H; Mancini, G; Lederer, D; Roscioli, T; Giuliano, F; Plomp, As; Rolfs, A; Graham, Jm; Seemanova, E; Poo, P; García-Cazorla, A; Edery, P; Jackson, Ij; Maher, Er; Aligianis, Ia.
Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes
2019-01-01 Mackay, Djg; Bliek, J; Lombardi, Mp; Russo, S; Calzari, L; Guzzetti, S; Izzi, C; Selicorni, A; Melis, D; Temple, K; Maher, E; Brioude, F; Netchine, I; Eggermann, T
Abdominal wall defects
2013-01-01 Prefumo, F; Izzi, C
Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature
2018-01-01 Agostini, A; Marchetti, D; Izzi, C; Cocco, I; Pinelli, L; Accorsi, P; Iascone Maria, R; Giordano, L
[Clinical diagnosis of Autosomal Dominant Polycystic Kidney Disease]
2016-01-01 Magistroni, R; Izzi, C; Scolari, F.
[Genetics and genetic counseling]
2016-01-01 Izzi, C; Liut, F; Dallera, N; Mazza, C; Magistroni, R; Savoldi, G; Scolari, F.
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis
2010-01-01 Micale, L; Turturo, Mg; Fusco, C; Augello, B; Jurado, La; Izzi, C; Digilio, Mc; Milani, D; Lapi, E; Zelante, L; Merla, G.
Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis
2015-01-01 Malvestiti, F; Agrati, C; Grimi, B; Pompilii, E; Izzi, C; Martinoni, L; Gaetani, E; Liuti, Mr; Trotta, A; Maggi, F; Simoni, G; Grati, Fr.
Identification of novel mutations in patients with fibrinogen disorders and genotype/phenotype correlations.
2019-01-01 Chinni, E; Tiscia, G; Favuzzi, G; Cappucci, F; Malcangi, G; Bagna, R; Izzi, C; Rizzi, D; De Stefano, V; Grandone, E.
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations
2013-01-01 Migliore, C; Athanasakis, E; Dahoun, S; Wonkam, A; Lees, M; Calabrese, O; Connell, F; Lynch, Sa; Izzi, C; Pompilii, E; Thakur, S; van Maarle, M; Wilson, Lc; Meroni, G.
Type I hyperprolinemia: genotype/phenotype correlations
2010-01-01 Guilmatre, A; Legallic, S; Steel, G; Willis, A; Di Rosa, G; Goldenberg, A; Drouin-Garraud, V; Guet, A; Mignot, C; Des Portes, V; Valayannopoulos, V; Van Maldergem, L; Hoffman, Jd; Izzi, C; Espil-Taris, C; Orcesi, S; Bonafé, L; Le Galloudec, E; Maurey, H; Ioos, C; Afenjar, A; Blanchet, P; Echenne, B; Roubertie, A; Frebourg, T; Valle, D; Campion, D
Design of a Multi-Mode Hybrid Micro-Gripper for Surface Mount Technology Component Assembly
2023-01-01 Fontana, Gianmauro; Iacono, Nicola; Pio Negri, Simone; Papadia, Gabriele
Divisione testamentaria incompleta e vis expansiva della institutio ex re certa
2023-01-01 Venturelli, Alberto
Heterogeneity in regional changes in body composition induced by androgen deprivation therapy in prostate cancer patients: potential impact on bone health-the BLADE study
2023-01-01 Dalla Volta, A; Palumbo, C; Zamboni, S; Mazziotti, G; Triggiani, L; Zamparini, M; Maffezzoni, F; Rinaudo, L; Bergamini, M; Di Meo, N; Caramella, I; Valcamonico, F; Borghetti, P; Guerini, A; Farina, D; Antonelli, A; Simeone, C; Berruti, A
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Lettera e legge. Il problema dell'interpretazione e del confine tra potere legislativo e potere giudiziario | 1-gen-2022 | Onorato, Michele | |
| Gli accordi ristrutturazione finanziari ai sensi dell'art. 186 septies l. fall. Dalla rottura di una equazione al paradosso di un caso | 1-gen-2016 | Onorato, Michele | |
| Donazione di beni altrui e donazione del bene presente nell'asse ereditario indiviso | 1-gen-2006 | Onorato, Michele | |
| Accordi a sfavore di terzo? Profili dei negozi sulla crisi d'impresa | 1-gen-2022 | Onorato, Michele | |
| L'errore ostativo | 1-gen-2005 | Onorato, Michele | |
| Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux | 1-gen-2021 | Verbitsky, M; Krithivasan, P; Batourina, E; Khan, A; Graham, Se; Marasà, M; Kim, H; Lim, Ty; Weng, Pl; Sánchez-Rodríguez, E; Mitrotti, A; Ahram, Df; Zanoni, F; Fasel, Da; Westland, R; Sampson, Mg; Zhang, Jy; Bodria, M; Kil, Bh; Shril, S; Gesualdo, L; Torri, F; Scolari, F; Izzi, C; van Wijk, Jae; Saraga, M; Santoro, D; Conti, G; Barton, De; Dobson, Mg; Puri, P; Furth, Sl; Warady, Ba; Pisani, I; Fiaccadori, E; Allegri, L; Degl'Innocenti, Ml; Piaggio, G; Alam, S; Gigante, M; Zaza, G; Esposito, P; Lin, F; Simões-E-Silva, Ac; Brodkiewicz, A; Drozdz, D; Zachwieja, K; Miklaszewska, M; Szczepanska, M; Adamczyk, P; Tkaczyk, M; Tomczyk, D; Sikora, P; Mizerska-Wasiak, M; Krzemien, G; Szmigielska, A; Zaniew, M; Lozanovski, Vj; Gucev, Z; Ionita-Laza, I; Stanaway, Ib; Crosslin, Dr; Wong, Cs; Hildebrandt, F; Barasch, J; Kenny, Ee; Loos, Rjf; Levy, B; Ghiggeri, Gm; Hakonarson, H; Latos-Bieleńska, A; Materna-Kiryluk, A; Darlow, Jm; Tasic, V; Willer, C; Kiryluk, K; Sanna-Cherchi, S; Mendelsohn, Cl; Gharavi, Ag | |
| Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome | 1-gen-2013 | Handley, Mt; Morris-Rosendahl, Dj; Brown, S; Macdonald, F; Hardy, C; Bem, D; Carpanini, Sm; Borck, G; Martorell, L; Izzi, C; Faravelli, F; Accorsi, P; Pinelli, L; Basel-Vanagaite, L; Peretz, G; Abdel-Salam, Gm; Zaki, Ms; Jansen, A; Mowat, D; Glass, I; Stewart, H; Mancini, G; Lederer, D; Roscioli, T; Giuliano, F; Plomp, As; Rolfs, A; Graham, Jm; Seemanova, E; Poo, P; García-Cazorla, A; Edery, P; Jackson, Ij; Maher, Er; Aligianis, Ia. | |
| Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes | 1-gen-2019 | Mackay, Djg; Bliek, J; Lombardi, Mp; Russo, S; Calzari, L; Guzzetti, S; Izzi, C; Selicorni, A; Melis, D; Temple, K; Maher, E; Brioude, F; Netchine, I; Eggermann, T | |
| Abdominal wall defects | 1-gen-2013 | Prefumo, F; Izzi, C | |
| Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature | 1-gen-2018 | Agostini, A; Marchetti, D; Izzi, C; Cocco, I; Pinelli, L; Accorsi, P; Iascone Maria, R; Giordano, L | |
| [Clinical diagnosis of Autosomal Dominant Polycystic Kidney Disease] | 1-gen-2016 | Magistroni, R; Izzi, C; Scolari, F. | |
| [Genetics and genetic counseling] | 1-gen-2016 | Izzi, C; Liut, F; Dallera, N; Mazza, C; Magistroni, R; Savoldi, G; Scolari, F. | |
| Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis | 1-gen-2010 | Micale, L; Turturo, Mg; Fusco, C; Augello, B; Jurado, La; Izzi, C; Digilio, Mc; Milani, D; Lapi, E; Zelante, L; Merla, G. | |
| Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis | 1-gen-2015 | Malvestiti, F; Agrati, C; Grimi, B; Pompilii, E; Izzi, C; Martinoni, L; Gaetani, E; Liuti, Mr; Trotta, A; Maggi, F; Simoni, G; Grati, Fr. | |
| Identification of novel mutations in patients with fibrinogen disorders and genotype/phenotype correlations. | 1-gen-2019 | Chinni, E; Tiscia, G; Favuzzi, G; Cappucci, F; Malcangi, G; Bagna, R; Izzi, C; Rizzi, D; De Stefano, V; Grandone, E. | |
| Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations | 1-gen-2013 | Migliore, C; Athanasakis, E; Dahoun, S; Wonkam, A; Lees, M; Calabrese, O; Connell, F; Lynch, Sa; Izzi, C; Pompilii, E; Thakur, S; van Maarle, M; Wilson, Lc; Meroni, G. | |
| Type I hyperprolinemia: genotype/phenotype correlations | 1-gen-2010 | Guilmatre, A; Legallic, S; Steel, G; Willis, A; Di Rosa, G; Goldenberg, A; Drouin-Garraud, V; Guet, A; Mignot, C; Des Portes, V; Valayannopoulos, V; Van Maldergem, L; Hoffman, Jd; Izzi, C; Espil-Taris, C; Orcesi, S; Bonafé, L; Le Galloudec, E; Maurey, H; Ioos, C; Afenjar, A; Blanchet, P; Echenne, B; Roubertie, A; Frebourg, T; Valle, D; Campion, D | |
| Design of a Multi-Mode Hybrid Micro-Gripper for Surface Mount Technology Component Assembly | 1-gen-2023 | Fontana, Gianmauro; Iacono, Nicola; Pio Negri, Simone; Papadia, Gabriele | |
| Divisione testamentaria incompleta e vis expansiva della institutio ex re certa | 1-gen-2023 | Venturelli, Alberto | |
| Heterogeneity in regional changes in body composition induced by androgen deprivation therapy in prostate cancer patients: potential impact on bone health-the BLADE study | 1-gen-2023 | Dalla Volta, A; Palumbo, C; Zamboni, S; Mazziotti, G; Triggiani, L; Zamparini, M; Maffezzoni, F; Rinaudo, L; Bergamini, M; Di Meo, N; Caramella, I; Valcamonico, F; Borghetti, P; Guerini, A; Farina, D; Antonelli, A; Simeone, C; Berruti, A |
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