S. Ravanbod

Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient

M. Jazebi, F. Ala, R. Schneppenheim, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of 123 previously unreported mutations in the F8 gene of Iranian patients with Haemophilia A

M. Jazebi, F. Ala, S. Ravanbod, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Extensive genetic screening of Iranian Factor FVII-deficient individuals unraveled several novel mutations and postulated founder effects in some cases

Hassan Rokni-Zadeh, S. Ravanbod, T. Shahani, 2022, Research and practice in thrombosis and haemostasis.

Seven novel point mutations in the F11 gene in Iranian FXI‐deficient patients

G. R. Lari, F. Ala, S. Ravanbod, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease

J. Emsley, M. Jazebi, M. Othman, 2012, Thrombosis and Haemostasis.

Identification of ten large deletions and one duplication in the F8 gene of eleven unrelated Iranian severe haemophilia A families using the multiplex ligation‐dependent probe amplification technique

M. Jazebi, S. Ghaffari, M. Rafati, 2011, Haemophilia.

How to deal with medical and social aspects of bleeding disorders – preparing women and the family in developing countries

F. Ala, S. Ravanbod, N. Cohan, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.