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Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with allele-specific mRNAs decay
2008-01-01 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
POSITIVE PROSTATE 68GAPSMA-PET/CT CORRELATES WITH DETECTION OF CD45-/PSMA(+) NON-SPERM EPITHELIAL CELLS OBTAINED BY LIQUID BIOPSY OF SEMINAL FLUID IN PATIENTS WITH PROSTATE CANCER (PCA).
2018-01-01 Lazzeri, M; Lopci, E; Lughezzani, G; Casale, P; Hurle, R; Saita, A; Peschechera, R; Benetti, A; Pasini, L; Zandegiacomo, S; Lista, G; Cardone, P; Chiti, A; Guazzoni, G; Colombo, F; Chiereghin, C; Asselta, R; Monterisi, S; Solda, G; Veronesi, G; Duga, S
Retrospective evaluation of dysfibrinogenaemic patients in a single centre: clinical features and laboratory findings
2009-01-01 Santoro, C; Leporace, A; Biondo, F; Asselta, R; Duga, S; Menegatti, M; Platè, M; Mazzucconi, M
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
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population
2010-01-01 Soldà, G; Oldoni, F; Asselta, R; Primignani, P; Castorina, P; Radaelli, C; Coviello, D; Duga, S
Severe factor V deficiency caused by two novel mutations in exon 13 of factor V gene
2000-01-01 Montefusco, Mc; Duga, S; Asselta, R; Malcovati, M; van Wijk, R; van Solinge, W; Santagostino, E; Tenchini, Ml; Mannucci, Pm
Severe factor V deficiency: identification and molecular characterization of three novel splicing mutations
2006-01-01 Asselta, R; Dall’Osso, C; Duga, S; Locatelli, N; Malcovati, M; Tenchini, Ml
Simultaneous genotyping of FXI type II and type III mutations by multiplex real-time PCR in healthy Italians and in FXI-deficient patients
2007-01-01 Zadra, G; Asselta, R; Tenchini, Ml; Seligsohn, U; Castaman, G; Duga, S
State of the art of rare bleeding disorders database (RBDD)
2008-01-01 Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F.
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population
2010-01-01 Guella, I; Trotta, L; Asselta, R; Solda', G; Zini, M; Zecchinelli, A; Pezzoli, G; Goldwurm, S; Duga, S
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with allele-specific mRNAs decay | 1-gen-2008 | Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R | |
| POSITIVE PROSTATE 68GAPSMA-PET/CT CORRELATES WITH DETECTION OF CD45-/PSMA(+) NON-SPERM EPITHELIAL CELLS OBTAINED BY LIQUID BIOPSY OF SEMINAL FLUID IN PATIENTS WITH PROSTATE CANCER (PCA). | 1-gen-2018 | Lazzeri, M; Lopci, E; Lughezzani, G; Casale, P; Hurle, R; Saita, A; Peschechera, R; Benetti, A; Pasini, L; Zandegiacomo, S; Lista, G; Cardone, P; Chiti, A; Guazzoni, G; Colombo, F; Chiereghin, C; Asselta, R; Monterisi, S; Solda, G; Veronesi, G; Duga, S | |
| Retrospective evaluation of dysfibrinogenaemic patients in a single centre: clinical features and laboratory findings | 1-gen-2009 | Santoro, C; Leporace, A; Biondo, F; Asselta, R; Duga, S; Menegatti, M; Platè, M; Mazzucconi, M | |
| 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 | |
| Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population | 1-gen-2010 | Soldà, G; Oldoni, F; Asselta, R; Primignani, P; Castorina, P; Radaelli, C; Coviello, D; Duga, S | |
| Severe factor V deficiency caused by two novel mutations in exon 13 of factor V gene | 1-gen-2000 | Montefusco, Mc; Duga, S; Asselta, R; Malcovati, M; van Wijk, R; van Solinge, W; Santagostino, E; Tenchini, Ml; Mannucci, Pm | |
| Severe factor V deficiency: identification and molecular characterization of three novel splicing mutations | 1-gen-2006 | Asselta, R; Dall’Osso, C; Duga, S; Locatelli, N; Malcovati, M; Tenchini, Ml | |
| Simultaneous genotyping of FXI type II and type III mutations by multiplex real-time PCR in healthy Italians and in FXI-deficient patients | 1-gen-2007 | Zadra, G; Asselta, R; Tenchini, Ml; Seligsohn, U; Castaman, G; Duga, S | |
| State of the art of rare bleeding disorders database (RBDD) | 1-gen-2008 | Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F. | |
| Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population | 1-gen-2010 | Guella, I; Trotta, L; Asselta, R; Solda', G; Zini, M; Zecchinelli, A; Pezzoli, G; Goldwurm, S; Duga, S |
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Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 68
- 1 Contributo su Rivista::1.5 Abst... 68
Data di pubblicazione
- 2010 - 2018 10
- 2000 - 2009 55
- 1998 - 1999 3
Editore
- Nature Publishing Group 4
- Blackwell 1
Rivista
- JOURNAL OF THROMBOSIS AND HAEMOST... 14
- EUROPEAN JOURNAL OF HUMAN GENETICS 11
- HAEMATOLOGICA 9
- BLOOD 8
- HAEMOPHILIA 7
- AMERICAN JOURNAL OF HUMAN GENETICS 3
- BLOOD TRANSFUSION 3
- THROMBOSIS AND HAEMOSTASIS 3
- CIRCULATION 2
- EUROPEAN JOURNAL OF CELL BIOLOGY 2
Lingua
- eng 65
Accesso al fulltext
- no fulltext 68