RicercaInizia una nuova ricerca
NOTA: è possibile cercare una corrispondenza esatta usando i doppi apici, ad es: "evoluzione della specie". Qualora si cerchi un identificativo, è consigliabile cercarlo in due modi differenti: tra apici con caratteri speciali es: "978-94-6366-274" oppure senza caratteri speciali solo come sequenza numerica: es 978946366274.
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
The double-faced association of the PRKCA gene with multiple sclerosis
2010-01-01 Paraboschi, E; Solda', G; Rimoldi, V; Dall’Osso, C; Anelli, G; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S; Asselta, R
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population
2009-01-01 Asselta, R; Paraboschi, E; Solda, G; Dall’Osso, C; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population
2008-01-01 Dall’Osso, C; Rizzo, G; Solda', G; Gemmati, D; Zamboni, P; Benedetti, Md; Salviati, A; Invernizzi, P; Bonissoni, S; Bolognesi, E; Bergamaschi, L; D’Alfonso, S; Duga, S; Tenchini, Ml; Asselta, R.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| The double-faced association of the PRKCA gene with multiple sclerosis | 1-gen-2010 | Paraboschi, E; Solda', G; Rimoldi, V; Dall’Osso, C; Anelli, G; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S; Asselta, R | |
| The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population | 1-gen-2009 | Asselta, R; Paraboschi, E; Solda, G; Dall’Osso, C; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S | |
| The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population | 1-gen-2008 | Dall’Osso, C; Rizzo, G; Solda', G; Gemmati, D; Zamboni, P; Benedetti, Md; Salviati, A; Invernizzi, P; Bonissoni, S; Bolognesi, E; Bergamaschi, L; D’Alfonso, S; Duga, S; Tenchini, Ml; Asselta, R. |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile
Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 63
- 1 Contributo su Rivista::1.5 Abst... 63
Data di pubblicazione
- 2010 - 2018 7
- 2000 - 2009 53
- 1998 - 1999 3
Editore
- Nature Publishing Group 4
- Blackwell 1
Rivista
- JOURNAL OF THROMBOSIS AND HAEMOST... 14
- EUROPEAN JOURNAL OF HUMAN GENETICS 11
- HAEMATOLOGICA 8
- BLOOD 7
- HAEMOPHILIA 7
- BLOOD TRANSFUSION 3
- THROMBOSIS AND HAEMOSTASIS 3
- AMERICAN JOURNAL OF HUMAN GENETICS 2
- EUROPEAN JOURNAL OF CELL BIOLOGY 2
- THE JOURNAL OF UROLOGY 2
Lingua
- eng 60
Accesso al fulltext
- no fulltext 63