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Journal of Thrombosis and Haemostasis : JTH
|
July 2, 2013
Future of coagulation factor replacement therapy
F Peyvandi, I Garagiola, S Seregni
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 22, 2017
Molecular diagnosis of von Willebrand disease
L Baronciani, A Goodeve, F Peyvandi
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 9, 2014
Does the orphan medicinal product regulation assist or hinder access to innovative haemophilia treatment in Europe?
B O'Mahony, F Peyvandi, A Bok
Reviews in Clinical and Experimental Hematology
|
February 15, 2002
Autosomal recessive deficiencies of coagulation factors
F Peyvandi, R Asselta, P M Mannucci
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
December 15, 2017
Acquired Von Willebrand syndrome and response to desmopressin
E Biguzzi, S M Siboni, F Peyvandi
British Journal of Haematology
|
February 13, 2001
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
M Lak, F Peyvandi, P M Mannucci
Journal of Thrombosis and Haemostasis : JTH
|
December 15, 2015
A critical appraisal of one-stage and chromogenic assays of factor VIII activity
F Peyvandi, J Oldenburg, K D Friedman
Journal of Thrombosis and Haemostasis : JTH
|
July 17, 2008
Dosing anticoagulant therapy with coumarin drugs: is genotyping clinically useful? No
P M Mannucci, M Spreafico, F Peyvandi
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 22, 2017
Reply to the letter by Iorio
P M Mannucci, F Peyvandi, F R Rosendaal
International Journal of Laboratory Hematology
|
October 14, 2017
Factor XIII deficiency diagnosis: Challenges and tools
M Karimi, F Peyvandi, M Naderi, et al.
Page
of 17
Search research articles
Search
Showing results (11-20 of 166) with videos related to
Sort By:
Page
of 17
Journal of Thrombosis and Haemostasis : JTH
|
July 2, 2013
Future of coagulation factor replacement therapy
F Peyvandi, I Garagiola, S Seregni
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 22, 2017
Molecular diagnosis of von Willebrand disease
L Baronciani, A Goodeve, F Peyvandi
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 9, 2014
Does the orphan medicinal product regulation assist or hinder access to innovative haemophilia treatment in Europe?
B O'Mahony, F Peyvandi, A Bok
Reviews in Clinical and Experimental Hematology
|
February 15, 2002
Autosomal recessive deficiencies of coagulation factors
F Peyvandi, R Asselta, P M Mannucci
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
December 15, 2017
Acquired Von Willebrand syndrome and response to desmopressin
E Biguzzi, S M Siboni, F Peyvandi
British Journal of Haematology
|
February 13, 2001
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
M Lak, F Peyvandi, P M Mannucci
Journal of Thrombosis and Haemostasis : JTH
|
December 15, 2015
A critical appraisal of one-stage and chromogenic assays of factor VIII activity
F Peyvandi, J Oldenburg, K D Friedman
Journal of Thrombosis and Haemostasis : JTH
|
July 17, 2008
Dosing anticoagulant therapy with coumarin drugs: is genotyping clinically useful? No
P M Mannucci, M Spreafico, F Peyvandi
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 22, 2017
Reply to the letter by Iorio
P M Mannucci, F Peyvandi, F R Rosendaal
International Journal of Laboratory Hematology
|
October 14, 2017
Factor XIII deficiency diagnosis: Challenges and tools
M Karimi, F Peyvandi, M Naderi, et al.
Page
of 17