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82篇 您的检索式：作者名="Peyvandi F"

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	题名	作者	年代	出处	被引量
1	CYP2C9 genotypes and does requirements during the induction phase of oral anticogulant therapy显示文摘	PEYVANDI F SPREAFICO M SIBONI S M	2004	Clin Pharmacol Ther2004，75，3：	1
2	Pathogenesis and treatment of ac- quired idiopathic thrombotic thrombocytopenic purpura 显示文摘	Peyvandi F Palla R Lotta LA	2010	Hae- matologica2010，95，9：	1
3	The thrombospondin- N700S polymorphism is associated with early myocardial in显示文摘	Zwicker JI Peyvandi F Palla R	2006	Blood2006，108，4：	1
4	Rare bleeding disorders:diagnosis and treatment显示文摘	Palla R Peyvandi F Shapiro AD	2015	Blood2015，125，13：	1
5	Dosing anticoagulant therapy with coumarin drugs: is genotypingclinically useful? No显示文摘	MANNUCCI PM SPREAFICO M PEYVANDI F	2008	J Thromb Haemost2008，9，1：	1
6	ADAMTS-13 assays in thrombotic thrombocytopenic purpura 显示文摘	Peyvandi F Palla R Lotta LA et aI	2010	J Thromb Haemost2010，8，4：	1
7	Dosing anticoagulant therapy with eoumarin drugs: is genotyping elinicaiIy useful? No 显示文摘	Mannucei PM Spreafieo M Peyvandi F	2008	J Thromh Haemost2008，6，9：	1
8	Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia显示文摘	Peyvandi F Haertel S Knaub S	2006	J Thromb Haemost2006，4，7：	1
9	Fibrinogen replacement therapy for congenital fibrinogen deficiency显示文摘	Bomikova L Peyvandi F Allen G	2011	J Thromb Haemost2011，9，：	1
10	Pathogenesis and treatment of acquired idiopathic thrombotic thrombocytopenic purpura显示文摘	Peyvandi F Palla R Lotta LA	2010	Haematologica2010，95，9：	1
11	Hemostasis and menstruation:appropriate investigation for underlying disorders of hemostasis in women with excessive menstrual bleeding显示文摘	Kouides PA Conard J Peyvandi F	2005	Fertil Steril2005，84，：	1
12	ADAMTS-13 assays in thrombotic thrombocytopenic purpura显示文摘	Peyvandi F Palla R Lotta LA	2010	J Thromb Haemost2010，8，4：	1
13	Recessively inherited coagulation disorders显示文摘	DUGA M PEYVANDI F	2004	Blood2004，104，：	1
14	Recessively inherited coagulation disorders显示文摘	MANNUCCI P M DUGA S PEYVANDI F	2004	Blood2004，104，：	1
15	Molecular characterisation and three-dimensional structural analysis of mutations in 21unrealted families with inherited factor Ⅶ deficiency显示文摘	Peyvandi F Jenkins PV Marmueci PM	2000	Thromb Haemost2000，84，2：	1
16	Role of yon Willebrand factor in the haemostasis显示文摘	Peyvandi F Garagiola I Baronciani L	2011	Blood Transfus2011，9，2：	1
17	CYP2C9 genotypes and dose requirements during the induction phase of oral anticoagulant therapy显示文摘	Peyvandi F Spreafico M Siboni SM	2004	Clin Pharmacol Ther2004，75，3：	1
18	Pathogenesis and treat- ment of acquired idiopathic thrombotic thrombocytopenic purpura显示文摘	Peyvandi F Palla R Lotta L A	2010	Haematologica2010，95，9：	1
19	Incidence of bleed- ing symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia显示文摘	Peyvandi F Haertel S Knaub S	2006	Thromb Haemost2006，4，7：	1
20	Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor Ⅶ deficiency 显示文摘	Peyvandi F Jenkins PV Mannucci PM	2000	Thromb Haemost2000，84，2：	1

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