76 Retroperitoneal and transperitoneal robotic assisted pyeloplasty in adults: Techniques and results
2010-01-01 Buffi, N; Cestari, A; Lista, G; Gadda, G; Sangalli, M; Scapaticci, E; Zanoni, M; Lazzeri, M; Guazzoni, G
Retrospective evaluation of dysifibrinogenemic patients at a single center: clinical features and laboratory findings
2009-01-01 Santoro, C; Leporace, Ap; Biondo, F; Plate, M; Asselta, R; Peyvandi, F; Menegatti, M; Pignoloni, P; Duga, S; Foa, R; Mazzucconi, Mg
Genotype dependent pattern of Peginterferon alfa-2B/Ribavirin treatment failure in hepatitis C virus infected patients with cirrhosis : a single centre study of 471 naïve patients
2008-01-01 Aghemo, A.; Rumi, M.; Monico, S.; Prati, G. M.; Ronchi, G.; Colombo, M.
Factor XI deficiency: identification and molecular characterization of six novel missense mutations
2006-01-01 Spena, S; Duga, S; Asselta, R; Ghiotto, R; Tagliaferri, A; Malcovati, M; Tenchini, Ml; Castaman, G
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy: a genetic analysis of 28 unrelated italian families
1998-01-01 Ferini-Strambi, L; Oldani, A; Zucconi, M; Asselta, R; Modugno, M; Duga, S; Bonati, Mt; Dalprà, L; Malcovati, M; Smirne, S; Tenchini, Ml
Identification of two novel missense mutations causing factor XI deficiency
2006-01-01 Duga, S; Asselta, R; Spena, S; Tagliaferri, A; Malcovati, M; Tenchini, Ml; Castaman, G
Family-based association analysis of the critical 3.4 Mb region on 17q24 reveals association between multiple sclerosis and the PRKCA gene
2004-01-01 Kallio, Sp; Saarela, J; Asselta, R; Chen, Dc; Jokiaho, A; Palotie, A; Peltonen, L
First identification of a splicing mutation in fibrinogen gamma-chain gene causing afibrinogenemia
2000-01-01 Asselta, R; Duga, S; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Allelic heterogeneity of severe factor V deficiency
2001-01-01 Montefusco, Mc; Duga, S; Asselta, R; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Evidence of the exixtance of at least a fourth locus for ADNFLE
2002-01-01 Combi, R; Duga, S; Asselta, R; Boi, S; Oldani, A; Zucconi, M; Ferini-Strambi, L; Malcovati, M; Dalprà, L; Tenchini, Ml
Allelic heterogeneity of severe factor V deficiency: doubling of the mutational spectrum of the factor V gene, and expression of the identified mutations
2003-01-01 Asselta, R; Montefusco, Mc; Duga, S; Peyvandi, F; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml
In vitro expression of a novel afibrinogenemia-causing missense mutation in the fibrinogen Bbeta-chain gene not associated with endoplasmic reticulum storage
2003-01-01 Asselta, R; Spena, S; Duga, S; Peyvandi, F; Mohanty, D; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Identification of the first missense mutation in the fibrinogen Aalpha-chain gene in a case of afibrinogenemia
2006-01-01 Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml.; Duga, S
Molecular characterization of an Italian cohort of 10 patients with type 3 Von Willebrand disease: expression studies of 3 missense mutations
2010-01-01 Solimando, M; Federici, Ab; Baronciani, L; Mussetti, A; Punzo, M; La Marca, S; Platè, M; Asselta, R; Peyvandi, F; Mannucci, Pm
The proprotein convertase subtilisin-kexin type 9 (PCSK9) R46L variant is associated with reduced serum low-density lipoprotein cholesterol in the Italian population
2007-01-01 Guella I, Duga S; Asselta, R; Rimordi, V; Peyvandi, F; Fetiveau, R; Merlini, Pa; Kathiresan, S; Ardissimo, D; Mannucci, Pm; on behalf of the ATVB, (Atherosclerosis; Thrombosis, ; Vascular Biology Italian Study, Group)
FDG PET-based response assessment before high-dose chemotherapy with peripheral blood stem cell and outcome, in patients with diffuse large B-cell lymphoma
2012-01-01 Castagna, L; Bramanti, S; Giordano, L; Chiti, A; Mauro, E; Gandolfi, S; Sarina, B; Todisco, E; Balzarotti, M; Stella, Cc; Santoro, A
Result of FDG PET Imaging After Chemotherapy +/- Immunotherapy Is a Significant and Independent Prognostic Indicator of Outcome for Patients with Follicular Lymphoma: Survey From a Single Institution
2011-01-01 Magagnoli, M; Mazza, R; Gandolfi, S; Rodari, M; Giordano, L; Anastasia, A; Lopci, E; Chiti, A; Santoro, A; Balzarotti, M
Platelet, but not skeletal muscle, mitochondrial function is altered in patients with septic shock
2012-01-01 Protti, A; Fortunato, F; Pluderi, M; Solimeno, Lp; Grimoldi, N; Lucchini, V; Tecchio, P; Comi, Gp; Caspani, ; Gattinoni, L.
VALUE OF FROZEN SECTIONS DURING NERVE-SPARING LAPAROSCOPIC RADICAL PROSTATECTOMY
2006-01-01 Naspro, R; Guazzoni, G; Freschi, M; Cestari, A; Salonia, A; Buffi, N; Montorsi, F; Rigatti, P
The effect of transfusion dependency and secondary iron overload on survival of patients with myelodysplastic syndrome
2005-01-01 DELLA PORTA, MATTEO GIOVANNI
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 76 Retroperitoneal and transperitoneal robotic assisted pyeloplasty in adults: Techniques and results | 1-gen-2010 | Buffi, N; Cestari, A; Lista, G; Gadda, G; Sangalli, M; Scapaticci, E; Zanoni, M; Lazzeri, M; Guazzoni, G | |
| Retrospective evaluation of dysifibrinogenemic patients at a single center: clinical features and laboratory findings | 1-gen-2009 | Santoro, C; Leporace, Ap; Biondo, F; Plate, M; Asselta, R; Peyvandi, F; Menegatti, M; Pignoloni, P; Duga, S; Foa, R; Mazzucconi, Mg | |
| Genotype dependent pattern of Peginterferon alfa-2B/Ribavirin treatment failure in hepatitis C virus infected patients with cirrhosis : a single centre study of 471 naïve patients | 1-gen-2008 | Aghemo, A.; Rumi, M.; Monico, S.; Prati, G. M.; Ronchi, G.; Colombo, M. | |
| Factor XI deficiency: identification and molecular characterization of six novel missense mutations | 1-gen-2006 | Spena, S; Duga, S; Asselta, R; Ghiotto, R; Tagliaferri, A; Malcovati, M; Tenchini, Ml; Castaman, G | |
| Autosomal Dominant Nocturnal Frontal Lobe Epilepsy: a genetic analysis of 28 unrelated italian families | 1-gen-1998 | Ferini-Strambi, L; Oldani, A; Zucconi, M; Asselta, R; Modugno, M; Duga, S; Bonati, Mt; Dalprà, L; Malcovati, M; Smirne, S; Tenchini, Ml | |
| Identification of two novel missense mutations causing factor XI deficiency | 1-gen-2006 | Duga, S; Asselta, R; Spena, S; Tagliaferri, A; Malcovati, M; Tenchini, Ml; Castaman, G | |
| Family-based association analysis of the critical 3.4 Mb region on 17q24 reveals association between multiple sclerosis and the PRKCA gene | 1-gen-2004 | Kallio, Sp; Saarela, J; Asselta, R; Chen, Dc; Jokiaho, A; Palotie, A; Peltonen, L | |
| First identification of a splicing mutation in fibrinogen gamma-chain gene causing afibrinogenemia | 1-gen-2000 | Asselta, R; Duga, S; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| Allelic heterogeneity of severe factor V deficiency | 1-gen-2001 | Montefusco, Mc; Duga, S; Asselta, R; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| Evidence of the exixtance of at least a fourth locus for ADNFLE | 1-gen-2002 | Combi, R; Duga, S; Asselta, R; Boi, S; Oldani, A; Zucconi, M; Ferini-Strambi, L; Malcovati, M; Dalprà, L; Tenchini, Ml | |
| Allelic heterogeneity of severe factor V deficiency: doubling of the mutational spectrum of the factor V gene, and expression of the identified mutations | 1-gen-2003 | Asselta, R; Montefusco, Mc; Duga, S; Peyvandi, F; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| In vitro expression of a novel afibrinogenemia-causing missense mutation in the fibrinogen Bbeta-chain gene not associated with endoplasmic reticulum storage | 1-gen-2003 | Asselta, R; Spena, S; Duga, S; Peyvandi, F; Mohanty, D; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| Identification of the first missense mutation in the fibrinogen Aalpha-chain gene in a case of afibrinogenemia | 1-gen-2006 | Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml.; Duga, S | |
| Molecular characterization of an Italian cohort of 10 patients with type 3 Von Willebrand disease: expression studies of 3 missense mutations | 1-gen-2010 | Solimando, M; Federici, Ab; Baronciani, L; Mussetti, A; Punzo, M; La Marca, S; Platè, M; Asselta, R; Peyvandi, F; Mannucci, Pm | |
| The proprotein convertase subtilisin-kexin type 9 (PCSK9) R46L variant is associated with reduced serum low-density lipoprotein cholesterol in the Italian population | 1-gen-2007 | Guella I, Duga S; Asselta, R; Rimordi, V; Peyvandi, F; Fetiveau, R; Merlini, Pa; Kathiresan, S; Ardissimo, D; Mannucci, Pm; on behalf of the ATVB, (Atherosclerosis; Thrombosis, ; Vascular Biology Italian Study, Group) | |
| FDG PET-based response assessment before high-dose chemotherapy with peripheral blood stem cell and outcome, in patients with diffuse large B-cell lymphoma | 1-gen-2012 | Castagna, L; Bramanti, S; Giordano, L; Chiti, A; Mauro, E; Gandolfi, S; Sarina, B; Todisco, E; Balzarotti, M; Stella, Cc; Santoro, A | |
| Result of FDG PET Imaging After Chemotherapy +/- Immunotherapy Is a Significant and Independent Prognostic Indicator of Outcome for Patients with Follicular Lymphoma: Survey From a Single Institution | 1-gen-2011 | Magagnoli, M; Mazza, R; Gandolfi, S; Rodari, M; Giordano, L; Anastasia, A; Lopci, E; Chiti, A; Santoro, A; Balzarotti, M | |
| Platelet, but not skeletal muscle, mitochondrial function is altered in patients with septic shock | 1-gen-2012 | Protti, A; Fortunato, F; Pluderi, M; Solimeno, Lp; Grimoldi, N; Lucchini, V; Tecchio, P; Comi, Gp; Caspani, ; Gattinoni, L. | |
| VALUE OF FROZEN SECTIONS DURING NERVE-SPARING LAPAROSCOPIC RADICAL PROSTATECTOMY | 1-gen-2006 | Naspro, R; Guazzoni, G; Freschi, M; Cestari, A; Salonia, A; Buffi, N; Montorsi, F; Rigatti, P | |
| The effect of transfusion dependency and secondary iron overload on survival of patients with myelodysplastic syndrome | 1-gen-2005 | DELLA PORTA, MATTEO GIOVANNI |
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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