Flora Peyvandi Selected Research

Afibrinogenemia (Fibrinogen Deficiency)

10/2003	Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene.
12/2002	Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites.
08/2002	Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.

3	Afibrinogenemia (Fibrinogen Deficiency) 10/2003 - 08/2002
2	Thrombotic Thrombocytopenic Purpura 02/2008 - 11/2004
1	Thrombosis (Thrombus) 08/2007
1	Conjunctivitis 01/2007
1	Myocardial Infarction 08/2006
1	Thrombophilia 07/2005
1	Factor VII Deficiency (Hypoproconvertinemia) 03/2005
1	Uniparental Disomy 11/2004
1	Inherited Blood Coagulation Disorders 09/2004
1	Factor X Deficiency 09/2004
1	Neoplasms (Cancer) 04/2003
1	Factor V Deficiency 01/2003

3	von Willebrand FactorIBA 08/2006 - 04/2003
3	BBeta fibrinogenIBA 10/2003 - 08/2002
2	Factor VII (Proconvertin)IBA 03/2005 - 09/2004
1	AntibodiesIBA 02/2008
1	AntigensIBA 08/2007
1	PlasminogenIBA 01/2007
1	DNA (Deoxyribonucleic Acid)IBA 07/2005
1	fibrinogen AalphaIBA 11/2004
1	AutoantibodiesIBA 11/2004
1	Fibrinogen (Factor I)IBA 10/2003
1	Factor V (Coagulation Factor V)IBA 01/2003
1	RNA Splice SitesIBA 12/2002