Flora Peyvandi
TitleCited byYear
Executive summary: heart disease and stroke statistics—2013 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, WB Borden, ...
Circulation 127 (1), 143-152, 2013
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ...
Nature genetics 43 (4), 333, 2011
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
S Kathiresan, BF Voight, S Purcell, K Musunuru, D Ardissino, ...
Nature genetics 41 (3), 334-341, 2009
Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies
M Scully, BJ Hunt, S Benjamin, R Liesner, P Rose, F Peyvandi, B Cheung, ...
British journal of haematology 158 (3), 323-335, 2012
New susceptibility locus for coronary artery disease on chromosome 3q22. 3
J Erdmann, A Großhennig, PS Braund, IR König, C Hengstenberg, ...
Nature genetics 41 (3), 280, 2009
Recessively inherited coagulation disorders
PM Mannucci, S Duga, F Peyvandi
Blood 104 (5), 1243-1252, 2004
The thrombogram in rare inherited coagulation disorders: its relation to clinical bleeding
R Al Dieri, F Peyvandi, E Santagostino, M Giansily, PM Mannucci, ...
Thrombosis and haemostasis 88 (10), 576-582, 2002
ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases
M Rieger, PM Mannucci, JAK Hovinga, A Herzog, G Gerstenbauer, ...
Blood 106 (4), 1262-1267, 2005
Rare coagulation deficiencies
F Peyvandi, S Duga, S Akhavan, PM Mannucci
Haemophilia 8 (3), 308-321, 2002
A randomized trial of factor VIII and neutralizing antibodies in hemophilia A
F Peyvandi, PM Mannucci, I Garagiola, A El-Beshlawy, M Elalfy, ...
New England Journal of Medicine 374 (21), 2054-2064, 2016
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders
F Peyvandi, R Palla, M Menegatti, SM Siboni, S Halimeh, B Faeser, ...
Journal of Thrombosis and Haemostasis 10 (4), 615-621, 2012
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia.
M Lak, M Keihani, F Elahi, F Peyvandi, PM Mannucci
British journal of haematology 107 (1), 204-206, 1999
ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission
F Peyvandi, S Lavoretano, R Palla, HB Feys, K Vanhoorelbeke, ...
haematologica 93 (2), 232-239, 2008
Rare coagulation disorders
F Peyvandi, PM Mannucci
Thrombosis and haemostasis 82 (10), 1207-1214, 1999
Caplacizumab for acquired thrombotic thrombocytopenic purpura
F Peyvandi, M Scully, JA Kremer Hovinga, S Cataland, P Knöbl, H Wu, ...
New England Journal of Medicine 374 (6), 511-522, 2016
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
M Lak, F Peyvandi, PM Mannucci
British journal of haematology 111 (4), 1236-1239, 2000
Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
G Mariani, FH Herrmann, A Dolce, A Batorova, D Etro, F Peyvandi, K Wulff, ...
Thrombosis and haemostasis 93 (03), 481-487, 2005
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group
Circulation 107 (8), 1117-1122, 2003
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium
Nature genetics 41 (3), 334, 2009
Evaluation and management of postpartum hemorrhage: consensus from an international expert panel
R Abdul‐Kadir, C McLintock, AS Ducloy, H El‐Refaey, A England, ...
Transfusion 54 (7), 1756-1768, 2014
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