Low risk of hepatitis B reactivatioin in patients with chronic hepatitis C and concurrent inactive hepatitis B infection treated with interferon and ribavirin
2008-01-01 Aghemo, A.; Viganò, M.; Iavarone, M.; Rumi, M. G.; Agnelli, F.; Lampertico, P.; Donato, M. F.; Colombo, M.
PROSTATECTOMIA RADICALE: L'EMOSTASI DEL PLESSO PROSTATICO CON ENDO GIA (4 ANNI DI ESPERIENZA)
1999-01-01 Muto, G; Bardari, F; Coppola, P; Cosma, L; Leggero, R; Giona, C; Dublino, M; Verdicchio, C; Biamino, G
Valutazione dell’onicopatia psoriasica e correlazione con il fenotipo clinico e l’artrite psoriasica: studio di 180 pazienti
2011-01-01 Brazzelli, V; Carugno, A; Cananzi, R; Borroni, R; Fornara, L; Alborghetti, A; Manna, V; Ronzi, G; Barbaccia, V; De Silvestri, A
P75 neurotrophin receptor restores defective apoptosis in psoriatic keratinocytes: a role for transit amplifying cells
2008-01-01 Marconi, A; Truzzi, F; Lotti, R; Dallaglio, K; Borroni, R; Vaschieri, C; Tiberio, R; Pincelli, C
Congenital afibrinogenemia: molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene
2006-01-01 Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml; Duga, S
First identification of a missense mutation in the D-domain of the fibrinogen beta chain in a case of congenital afibrinogenemia
1999-01-01 Duga, S; Asselta, R; Simonic, T; Santagostino, E; Mannucci, Pm; Malcovati, M; Tenchini, Ml
From Owren’s first parahemophilia case to present, characterization of missense mutations in the factor V gene by in vitro expression
2003-01-01 Duga, S; Asselta, R; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml
A new genetic mechanism for congenital afibrinogenemia: maternal uniparental isodisomy for chromosome 4 containing a 15-kb deletion in fibrinogen Aalpha-chain gene
2004-01-01 Duga, S; Spena, S; Asselta, R; Peyandi, F; Mahasandana, C; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: identification of five new point mutations leading to Aalpha-chain truncations
2000-01-01 Duga, S; Asselta, R; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene causing afibrinogenemia
2006-01-01 Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml; Duga, S
Molecular characterization of three novel splicing mutations causing severe factor V deficiency
2006-01-01 Asselta, R; Dall’Osso, C; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml
The Use of High Resolution Melting (HRM) Analysis for Molecular Gene Defects of Type 3 Von Willebrand Disease: Studies of An Italian Cohort of 10 Patients
2009-01-01 Solimando, M; Federici, Ab; Baronciani, L; Mussetti, A; Punzo, M; La Marca, S; Plate, M; Asselta, R; Mannucci, Pm
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction
2008-01-01 Guella, I; Rimoldi, V; Merlini, Pa; Asselta, R; Paraboschi, Em; Francolini, M; Peyvandi, F; Ardissimo, D; Mannucci, Pm; Duga, S
Database on Rare Bleeding Disorder (RBDs): phenotype and genotype analysis on 400 affected patients
2007-01-01 Spreafico, M; Menegatti, M; Garagiola, I; Palla, R; Tagliabue, L; Karimi, M; Lak, M; Srivastava, A; Saxena, R; Shetty, S; Kavakly, K; Dolnicar, Mb; Aronis-Vournas, S; Asselta, R; Duga, S; Mannucci, Pm; Peyvandi, F
NPLA3 I148M polymorphism, steatosis, liver damage, and treatment response in chronic hepatitis C
2010-01-01 Valenti, L. V. C.; Rumi, M.; Galmozzi, E.; Del Menico, B.; De Nicola, S.; Dongiovanni, P.; Maggioni, M.; Fracanzani, A. L.; Rametta, R.; Colombo, M.; Fargion, S. R.; Aghemo, A. M.
VMAT SBRT For Localized Prostate Cancer: 4-Year Follow-Up And Correlation With WHO2016 Grade Groups
2018-01-01 D'Agostino, Gr; Di Brina, L; Franzese, C; Franceschini, D; Clerici, E; Tomatis, S; Iftode, C; Tozzi, A; Navarria, P; De Rose, F; Comito, T; Scorsetti, M
TRANSURETRAL ELECTROVAPORIZATION OF THE PROSTATE (TVP) A MULTICENTRIC RANDOMIZED COMPARATIVE STUDY VS TURP
1996-01-01 Puppo, P; Perachino, M; Breda, G; Boccafoschi, C; Coneri, F; Francesca, F; Gallucci, M; Graziotti, Pp; Guazzieri, G; Lembo, M; Mandressi, A; Muto, G
Ductal carcinoma in situ treated with breast conservative surgery and radiotherapy: A national multicentre experience
2018-01-01 Meattini, I; Pasinetti, N; Meduri, B; De Rose, F; De Santis, Mc; Lancellotta, V; Rossi, F; Franco, P; Alongi, F; Saieva, C; Delli Paoli, C; Desideri, I; D'Angelo, E; Triggiani, L; Ricardi, U; Bastiani, P; Aristei, C; Lozza, L; Scorsetti, M; Livi, L
Role of SBRT in the treatment of liver metastases: clinical results and prognostic factors
2018-01-01 Clerici, E; Comito, T; Franzese, C; Di Brina, L; Iftode, C; Tozzi, A; De Rose, F; Navarria, P; D'Agostino, Gr; Scorsetti, M
Neuroendocrine Liver Metastasis: A Novel Nomogram Predicting the Prognosis of Patients after Liver Resection
2016-01-01 Ruzzenente, Andrea; Bagante, Fabio; Bertuzzo, Francesca; Aldrighetti, Luca; Ercolani, Giorgio; Ferrero, Alessandro; Giuliante, Felice; Torzilli, G; Grazi Gian, Luca; Guglielmi, Alfredo; Iacono, Calogero
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Low risk of hepatitis B reactivatioin in patients with chronic hepatitis C and concurrent inactive hepatitis B infection treated with interferon and ribavirin | 1-gen-2008 | Aghemo, A.; Viganò, M.; Iavarone, M.; Rumi, M. G.; Agnelli, F.; Lampertico, P.; Donato, M. F.; Colombo, M. | |
| PROSTATECTOMIA RADICALE: L'EMOSTASI DEL PLESSO PROSTATICO CON ENDO GIA (4 ANNI DI ESPERIENZA) | 1-gen-1999 | Muto, G; Bardari, F; Coppola, P; Cosma, L; Leggero, R; Giona, C; Dublino, M; Verdicchio, C; Biamino, G | |
| Valutazione dell’onicopatia psoriasica e correlazione con il fenotipo clinico e l’artrite psoriasica: studio di 180 pazienti | 1-gen-2011 | Brazzelli, V; Carugno, A; Cananzi, R; Borroni, R; Fornara, L; Alborghetti, A; Manna, V; Ronzi, G; Barbaccia, V; De Silvestri, A | |
| P75 neurotrophin receptor restores defective apoptosis in psoriatic keratinocytes: a role for transit amplifying cells | 1-gen-2008 | Marconi, A; Truzzi, F; Lotti, R; Dallaglio, K; Borroni, R; Vaschieri, C; Tiberio, R; Pincelli, C | |
| Congenital afibrinogenemia: molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene | 1-gen-2006 | Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml; Duga, S | |
| First identification of a missense mutation in the D-domain of the fibrinogen beta chain in a case of congenital afibrinogenemia | 1-gen-1999 | Duga, S; Asselta, R; Simonic, T; Santagostino, E; Mannucci, Pm; Malcovati, M; Tenchini, Ml | |
| From Owren’s first parahemophilia case to present, characterization of missense mutations in the factor V gene by in vitro expression | 1-gen-2003 | Duga, S; Asselta, R; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml | |
| A new genetic mechanism for congenital afibrinogenemia: maternal uniparental isodisomy for chromosome 4 containing a 15-kb deletion in fibrinogen Aalpha-chain gene | 1-gen-2004 | Duga, S; Spena, S; Asselta, R; Peyandi, F; Mahasandana, C; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| Congenital afibrinogenemia: identification of five new point mutations leading to Aalpha-chain truncations | 1-gen-2000 | Duga, S; Asselta, R; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene causing afibrinogenemia | 1-gen-2006 | Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml; Duga, S | |
| Molecular characterization of three novel splicing mutations causing severe factor V deficiency | 1-gen-2006 | Asselta, R; Dall’Osso, C; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml | |
| The Use of High Resolution Melting (HRM) Analysis for Molecular Gene Defects of Type 3 Von Willebrand Disease: Studies of An Italian Cohort of 10 Patients | 1-gen-2009 | Solimando, M; Federici, Ab; Baronciani, L; Mussetti, A; Punzo, M; La Marca, S; Plate, M; Asselta, R; Mannucci, Pm | |
| Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction | 1-gen-2008 | Guella, I; Rimoldi, V; Merlini, Pa; Asselta, R; Paraboschi, Em; Francolini, M; Peyvandi, F; Ardissimo, D; Mannucci, Pm; Duga, S | |
| Database on Rare Bleeding Disorder (RBDs): phenotype and genotype analysis on 400 affected patients | 1-gen-2007 | Spreafico, M; Menegatti, M; Garagiola, I; Palla, R; Tagliabue, L; Karimi, M; Lak, M; Srivastava, A; Saxena, R; Shetty, S; Kavakly, K; Dolnicar, Mb; Aronis-Vournas, S; Asselta, R; Duga, S; Mannucci, Pm; Peyvandi, F | |
| NPLA3 I148M polymorphism, steatosis, liver damage, and treatment response in chronic hepatitis C | 1-gen-2010 | Valenti, L. V. C.; Rumi, M.; Galmozzi, E.; Del Menico, B.; De Nicola, S.; Dongiovanni, P.; Maggioni, M.; Fracanzani, A. L.; Rametta, R.; Colombo, M.; Fargion, S. R.; Aghemo, A. M. | |
| VMAT SBRT For Localized Prostate Cancer: 4-Year Follow-Up And Correlation With WHO2016 Grade Groups | 1-gen-2018 | D'Agostino, Gr; Di Brina, L; Franzese, C; Franceschini, D; Clerici, E; Tomatis, S; Iftode, C; Tozzi, A; Navarria, P; De Rose, F; Comito, T; Scorsetti, M | |
| TRANSURETRAL ELECTROVAPORIZATION OF THE PROSTATE (TVP) A MULTICENTRIC RANDOMIZED COMPARATIVE STUDY VS TURP | 1-gen-1996 | Puppo, P; Perachino, M; Breda, G; Boccafoschi, C; Coneri, F; Francesca, F; Gallucci, M; Graziotti, Pp; Guazzieri, G; Lembo, M; Mandressi, A; Muto, G | |
| Ductal carcinoma in situ treated with breast conservative surgery and radiotherapy: A national multicentre experience | 1-gen-2018 | Meattini, I; Pasinetti, N; Meduri, B; De Rose, F; De Santis, Mc; Lancellotta, V; Rossi, F; Franco, P; Alongi, F; Saieva, C; Delli Paoli, C; Desideri, I; D'Angelo, E; Triggiani, L; Ricardi, U; Bastiani, P; Aristei, C; Lozza, L; Scorsetti, M; Livi, L | |
| Role of SBRT in the treatment of liver metastases: clinical results and prognostic factors | 1-gen-2018 | Clerici, E; Comito, T; Franzese, C; Di Brina, L; Iftode, C; Tozzi, A; De Rose, F; Navarria, P; D'Agostino, Gr; Scorsetti, M | |
| Neuroendocrine Liver Metastasis: A Novel Nomogram Predicting the Prognosis of Patients after Liver Resection | 1-gen-2016 | Ruzzenente, Andrea; Bagante, Fabio; Bertuzzo, Francesca; Aldrighetti, Luca; Ercolani, Giorgio; Ferrero, Alessandro; Giuliante, Felice; Torzilli, G; Grazi Gian, Luca; Guglielmi, Alfredo; Iacono, Calogero |
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Scopri
Tipologia
- 1 Contributo su Rivista2157
Data di pubblicazione
- 2020 - 2025111
- 2010 - 20191343
- 2000 - 2009591
- 1990 - 1999111
- 1988 - 19891
Editore
- Nature Publishing Group4
- s.n4
- ICRS3
- Blackwell1
Rivista
- EUROPEAN UROLOGY. SUPPLEMENTS124
- GASTROENTEROLOGY123
- EUROPEAN JOURNAL OF NUCLEAR MEDIC...120
- THE JOURNAL OF UROLOGY111
- DIGESTIVE AND LIVER DISEASE100
- THE JOURNAL OF NUCLEAR MEDICINE80
- ANNALS OF THE RHEUMATIC DISEASES69
- RADIOTHERAPY AND ONCOLOGY59
- ANNALS OF ONCOLOGY57
- JOURNAL OF CLINICAL ONCOLOGY45
Keyword
- Myelodysplastic syndrome8
- Survival4
- biomimetic3
- Mitochondrial ferritin3
- osteochondral3
- Prognosis3
- scaffold3
- Sideroblastic anemia3
- viscosupplementation3
- COLONOSCOPIC SURVEILLANCE2
Lingua
- eng798
- ita24
- und6
Accesso al fulltext
- no fulltext2104
- reserved51
- open2