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Heredity|October 3, 1999
Sequence-tagged-site (STS) markers of arbitrary genes: the amount and nature of variation revealed in Norway spruceD J Perry, N Isabel, J Bousquet
Thrombosis and Haemostasis|May 1, 1996
Factor V (Arg 506-->Gln) mutation in young survivors of myocardial infarctionD Ardissino, F Peyvandi, P A Merlini, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 6, 2007
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in IndiaG Jayandharan, M Spreafico, A Viswabandya, et al.
Journal of Thrombosis and Haemostasis : JTH|June 30, 2011
Fibrinogen replacement therapy for congenital fibrinogen deficiencyL Bornikova, F Peyvandi, G Allen, et al.
American Journal of Hematology|September 25, 2004
Presentation and pattern of symptoms in 382 patients with Glanzmann thrombasthenia in IranG Toogeh, R Sharifian, M Lak, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 5, 2016
Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand diseaseS M Siboni, E Biguzzi, V Caiani, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 3, 2004
Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and ItalyM Karimi, F Peyvandi, S Siboni, et al.
Blood|February 9, 1999
Characterization of two naturally occurring mutations in the second epidermal growth factor-like domain of factor VIIM Hunault, A A Arbini, J A Carew, et al.
British Journal of Haematology|April 8, 1998
Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIIIF Peyvandi, E G Tuddenham, A M Akhtari, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 24, 2017
A comparative evaluation of a new fully automated assay for von Willebrand factor collagen binding activity to an established methodF Stufano, L Baronciani, D Mane-Padros, et al.
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