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Human Mutation
|
October 23, 2009
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura
Luca A Lotta, Isabella Garagiola, Roberta Palla, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 12, 2025
The genetic spectrum of rare bleeding disorders
Samin Mohsenian, Omid Seidizadeh, Andrea Cairo, et al.
Blood
|
August 4, 2017
Genetic risk stratification to reduce inhibitor development in the early treatment of hemophilia A: a SIPPET analysis
Frits R Rosendaal, Roberta Palla, Isabella Garagiola, et al.
Thrombosis Research
|
November 18, 2016
Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders
Roberta Palla, Simona M Siboni, Marzia Menegatti, et al.
Thrombosis and Haemostasis
|
November 25, 2010
Evaluation of assay methods to measure plasma ADAMTS13 activity in thrombotic microangiopathies
Roberta Palla, Carla Valsecchi, Mariateresa Bajetta, et al.
Blood Transfusion = Trasfusione Del Sangue
|
July 8, 2017
High-titre inhibitors in previously untreated patients with severe haemophilia A receiving recombinant or plasma-derived factor VIII: a budget-impact analysis
Andrea Messori, Flora Peyvandi, Sabrina Trippoli, et al.
Pediatric Blood & Cancer
|
October 12, 2013
Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish children
Ayse Metin, Sule Unal, Fatma Gümrük, et al.
Blood Transfusion = Trasfusione Del Sangue
|
January 13, 2018
Further comments on "High-titre inhibitors in previously untreated patients with severe haemophilia A receiving recombinant or plasma-derived factor VIII: a budget-impact analysis"
Andrea Messori, Flora Peyvandi, Sabrina Trippoli, et al.
Biophysical Journal
|
May 27, 2008
Mechanistic studies on ADAMTS13 catalysis
Enrico Di Stasio, Stefano Lancellotti, Flora Peyvandi, et al.
Blood
|
December 31, 2016
Nonneutralizing antibodies against factor VIII and risk of inhibitor development in severe hemophilia A
Antonino Cannavò, Carla Valsecchi, Isabella Garagiola, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
Human Mutation
|
October 23, 2009
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura
Luca A Lotta, Isabella Garagiola, Roberta Palla, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 12, 2025
The genetic spectrum of rare bleeding disorders
Samin Mohsenian, Omid Seidizadeh, Andrea Cairo, et al.
Blood
|
August 4, 2017
Genetic risk stratification to reduce inhibitor development in the early treatment of hemophilia A: a SIPPET analysis
Frits R Rosendaal, Roberta Palla, Isabella Garagiola, et al.
Thrombosis Research
|
November 18, 2016
Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders
Roberta Palla, Simona M Siboni, Marzia Menegatti, et al.
Thrombosis and Haemostasis
|
November 25, 2010
Evaluation of assay methods to measure plasma ADAMTS13 activity in thrombotic microangiopathies
Roberta Palla, Carla Valsecchi, Mariateresa Bajetta, et al.
Blood Transfusion = Trasfusione Del Sangue
|
July 8, 2017
High-titre inhibitors in previously untreated patients with severe haemophilia A receiving recombinant or plasma-derived factor VIII: a budget-impact analysis
Andrea Messori, Flora Peyvandi, Sabrina Trippoli, et al.
Pediatric Blood & Cancer
|
October 12, 2013
Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish children
Ayse Metin, Sule Unal, Fatma Gümrük, et al.
Blood Transfusion = Trasfusione Del Sangue
|
January 13, 2018
Further comments on "High-titre inhibitors in previously untreated patients with severe haemophilia A receiving recombinant or plasma-derived factor VIII: a budget-impact analysis"
Andrea Messori, Flora Peyvandi, Sabrina Trippoli, et al.
Biophysical Journal
|
May 27, 2008
Mechanistic studies on ADAMTS13 catalysis
Enrico Di Stasio, Stefano Lancellotti, Flora Peyvandi, et al.
Blood
|
December 31, 2016
Nonneutralizing antibodies against factor VIII and risk of inhibitor development in severe hemophilia A
Antonino Cannavò, Carla Valsecchi, Isabella Garagiola, et al.
Page
of 5