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Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study
2018-01-01 Rossi, M; Meggendorfer, M; Zampini, M; Tettamanti, M; Riva, E; Saba, E; Manes, N; Milanesi, C; Marta, U; Morabito, L; Travaglino, E; Peano, C; Giulia, S; Asselta, R; Duga, S; Malik, K; Selmi, C; Civilini, E; Mandelli, S; Bolli, N; Vassiliou, Gs; Kern, W; Santoro, A; Lucca, U; Haferlach, T; Della Porta, M
Congenital afibrinogenemia caused by uniparental isodisomy of chromosome 4 containing a 15-kb deletion involving fibrinogen Aalpha-chain gene
2004-01-01 Spena, S; Duga, S; Asselta, R; Malcovati, M; Tenchini, Ml
Congenital afibrinogenemia, identification of four novel homozygous mutations in the fibrinogen gene cluster: three point mutations and a 15-kb deletion
2003-01-01 Duga, S; Asselta, R; Spena, S; Peyvandi, F; 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
Congenital afibrinogenemia: In Vitro Expression of Two Novel Missense Mutations in the Fibrinogen Bbeta-Chain Gene Demonstrates That One of Them Acts as a Splicing Mutation
2002-01-01 Asselta, R; Spena, S; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml
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
Congenital afibrinogenemia: two novel fibrinogen gene mutations identified in two patients from Iran
2006-01-01 Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml
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
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients
2009-01-01 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
Eight novel mutations in FXI gene
2005-01-01 G., Castaman; R., Ghiotto; G., Rossetti; D., Habart; A., Tagliaferri; Duga, S
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study | 1-gen-2018 | Rossi, M; Meggendorfer, M; Zampini, M; Tettamanti, M; Riva, E; Saba, E; Manes, N; Milanesi, C; Marta, U; Morabito, L; Travaglino, E; Peano, C; Giulia, S; Asselta, R; Duga, S; Malik, K; Selmi, C; Civilini, E; Mandelli, S; Bolli, N; Vassiliou, Gs; Kern, W; Santoro, A; Lucca, U; Haferlach, T; Della Porta, M | |
| Congenital afibrinogenemia caused by uniparental isodisomy of chromosome 4 containing a 15-kb deletion involving fibrinogen Aalpha-chain gene | 1-gen-2004 | Spena, S; Duga, S; Asselta, R; Malcovati, M; Tenchini, Ml | |
| Congenital afibrinogenemia, identification of four novel homozygous mutations in the fibrinogen gene cluster: three point mutations and a 15-kb deletion | 1-gen-2003 | Duga, S; Asselta, R; Spena, S; Peyvandi, F; 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 | |
| Congenital afibrinogenemia: In Vitro Expression of Two Novel Missense Mutations in the Fibrinogen Bbeta-Chain Gene Demonstrates That One of Them Acts as a Splicing Mutation | 1-gen-2002 | Asselta, R; Spena, S; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml | |
| 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 | |
| Congenital afibrinogenemia: two novel fibrinogen gene mutations identified in two patients from Iran | 1-gen-2006 | Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml | |
| 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 | |
| Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients | 1-gen-2009 | Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R | |
| Eight novel mutations in FXI gene | 1-gen-2005 | G., Castaman; R., Ghiotto; G., Rossetti; D., Habart; A., Tagliaferri; Duga, S |
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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