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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
Factor V Leiden is associated with premature myocardial infarction
2008-01-01 Peyvandi, F.; Spreafico, M.; Foco, L.; Bernardinelli, L.; Duga, S.; Asselta, R.; Ardissino, D.; Kathiresan, S.; Merlini, P. A.; Mannucci, P. M.
Factor V Leiden, but not prothrombin G20120A, is associated with premature myocardial infarction
2008-01-01 Spreafico, M.; Peyvandi, F.; Foco, L.; Bernardinelli, L.; Duga, S.; Asselta, R.; Ardissino, D.; Kathiresan, S.; Merlini, P. A.; Mannucci, P. 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
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
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
Five new point mutations in fibrinogen alpha-chain gene causing afibrinogenemia
2000-01-01 Asselta, R; Duga, S; Malcovati, M; Simonic, T; Santagostino, E; Mannucci, Pm; 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
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
Genetic defects in congenital afibrinogenemia
2002-01-01 Asselta, R; Spena, S; Duga, S; Tenchini, Ml
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
Factor V Leiden is associated with premature myocardial infarction | 1-gen-2008 | Peyvandi, F.; Spreafico, M.; Foco, L.; Bernardinelli, L.; Duga, S.; Asselta, R.; Ardissino, D.; Kathiresan, S.; Merlini, P. A.; Mannucci, P. M. | |
Factor V Leiden, but not prothrombin G20120A, is associated with premature myocardial infarction | 1-gen-2008 | Spreafico, M.; Peyvandi, F.; Foco, L.; Bernardinelli, L.; Duga, S.; Asselta, R.; Ardissino, D.; Kathiresan, S.; Merlini, P. A.; Mannucci, P. 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 | |
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 | |
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 | |
Five new point mutations in fibrinogen alpha-chain gene causing afibrinogenemia | 1-gen-2000 | Asselta, R; Duga, S; Malcovati, M; Simonic, T; Santagostino, E; Mannucci, Pm; 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 | |
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 | |
Genetic defects in congenital afibrinogenemia | 1-gen-2002 | Asselta, R; Spena, S; Duga, S; Tenchini, Ml |
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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