Sfoglia per Rivista HAEMOPHILIA
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.
Test-retest reliability of a mobile application of the patient reported outcomes burdens and experiences (PROBE) study
2024-01-01 Curtis, Randall; Wu, Joanne; Iorio, Alfonso; Frick, Neil; Nichol, Michael; Noone, Declan; O'Mahony, Brian; Page, David; Stonebraker, Jeffrey; Kucher, Alexandra; Clearfield, Elizabeth; Skinner, Mark W; Germini, Federico
The spectrum of FXI deficiency in Italy
2014-01-01 Castaman, G; Giacomelli, Sh; Caccia, S; Riccardi, F; Rossetti, G; Dragani, A; Giuffrida, Ac; Biasoli, C; Duga, S
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients
2006-01-01 Monaldini, L; Duga, S; Asselta, R; Peyvandi, F; Karimi, M; Malcovati, M; Tenchini, Ml
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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. | |
| Test-retest reliability of a mobile application of the patient reported outcomes burdens and experiences (PROBE) study | 1-gen-2024 | Curtis, Randall; Wu, Joanne; Iorio, Alfonso; Frick, Neil; Nichol, Michael; Noone, Declan; O'Mahony, Brian; Page, David; Stonebraker, Jeffrey; Kucher, Alexandra; Clearfield, Elizabeth; Skinner, Mark W; Germini, Federico | |
| The spectrum of FXI deficiency in Italy | 1-gen-2014 | Castaman, G; Giacomelli, Sh; Caccia, S; Riccardi, F; Rossetti, G; Dragani, A; Giuffrida, Ac; Biasoli, C; Duga, S | |
| Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients | 1-gen-2006 | Monaldini, L; Duga, S; Asselta, R; Peyvandi, F; Karimi, M; Malcovati, M; Tenchini, Ml |
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