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F Peyvandi

Showing results (61-70 of 166) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|June 6, 2018
Choices of factor VIII products in previously untreated patients with haemophilia A: A global surveyF Peyvandi, R Palla, C Franchi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 14, 2013
A two-centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigenF Stufano, A S Lawrie, S La Marca, et al.
International Journal of Laboratory Hematology|August 3, 2017
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratoriesI Jennings, S Kitchen, M Menegatti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 26, 2018
Differential diagnosis between type 2A and 2B von Willebrand disease in a child with a previously undescribed de novo mutationM T Pagliari, L Baronciani, F Stufano, et al.
Journal of Thrombosis and Haemostasis : JTH|October 29, 2017
Timing and severity of inhibitor development in recombinant versus plasma-derived factor VIII concentrates: a SIPPET analysisF Peyvandi, A Cannavò, I Garagiola, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 20, 2016
New findings on inhibitor development: from registries to clinical studiesF Peyvandi, C E Ettingshausen, J Goudemand, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiencyF Peyvandi, P M Mannucci, D Asti, et al.
Thrombosis and Haemostasis|November 13, 2002
Allele frequency of CYP2C9 gene polymorphisms in IranF Peyvandi, M Spreafico, M Karimi, et al.
International Journal of Laboratory Hematology|April 14, 2017
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratoriesI Jennings, S Kitchen, M Menegatti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 29, 2014
Management of pregnancy in type 2B von Willebrand disease: case report and literature reviewE Biguzzi, S M Siboni, M W Ossola, et al.
Pageof 17

Showing results (61-70 of 166) with videos related to

Sort By:
Pageof 17
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 6, 2018
Choices of factor VIII products in previously untreated patients with haemophilia A: A global surveyF Peyvandi, R Palla, C Franchi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 14, 2013
A two-centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigenF Stufano, A S Lawrie, S La Marca, et al.
International Journal of Laboratory Hematology|August 3, 2017
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratoriesI Jennings, S Kitchen, M Menegatti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 26, 2018
Differential diagnosis between type 2A and 2B von Willebrand disease in a child with a previously undescribed de novo mutationM T Pagliari, L Baronciani, F Stufano, et al.
Journal of Thrombosis and Haemostasis : JTH|October 29, 2017
Timing and severity of inhibitor development in recombinant versus plasma-derived factor VIII concentrates: a SIPPET analysisF Peyvandi, A Cannavò, I Garagiola, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 20, 2016
New findings on inhibitor development: from registries to clinical studiesF Peyvandi, C E Ettingshausen, J Goudemand, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiencyF Peyvandi, P M Mannucci, D Asti, et al.
Thrombosis and Haemostasis|November 13, 2002
Allele frequency of CYP2C9 gene polymorphisms in IranF Peyvandi, M Spreafico, M Karimi, et al.
International Journal of Laboratory Hematology|April 14, 2017
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratoriesI Jennings, S Kitchen, M Menegatti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 29, 2014
Management of pregnancy in type 2B von Willebrand disease: case report and literature reviewE Biguzzi, S M Siboni, M W Ossola, et al.
Pageof 17