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Suhair S Eid

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Clinical Laboratory Science : Journal of the American Society for Medical Technology|June 5, 2003
Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patientsSuhair S Eid
Clinical Laboratory Science : Journal of the American Society for Medical Technology|November 24, 2004
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy JordaniansSuhair S Eid, Ghada Rihani
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 12, 2005
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patientsSuhair S Eid, Taisir Shubeilat
Clinical Laboratory Science : Journal of the American Society for Medical Technology|January 30, 2009
Inherited bleeding disorders: a 14-year retrospective studySuhair S Eid, Nazmi R Kamal, Taisir S Shubeilat, et al.
Human Reproduction (Oxford, England)|July 13, 2006
Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failureHussein S Qublan, Suhair S Eid, Hani A Ababneh, et al.
European Journal of Haematology|January 17, 2016
Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individualsMing Y Lim, Allison M Deal, Steven Kim, et al.
Human Mutation|October 8, 2009
Widening the mutation spectrum of EVC and EVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts Hedgehog signalingMaria Valencia, Pablo Lapunzina, Derek Lim, et al.
European Journal of Epidemiology|August 1, 2013
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controlsBenedetto Simone, Valerio De Stefano, Emanuele Leoncini, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Clinical Laboratory Science : Journal of the American Society for Medical Technology|June 5, 2003
Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patientsSuhair S Eid
Clinical Laboratory Science : Journal of the American Society for Medical Technology|November 24, 2004
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy JordaniansSuhair S Eid, Ghada Rihani
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 12, 2005
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patientsSuhair S Eid, Taisir Shubeilat
Clinical Laboratory Science : Journal of the American Society for Medical Technology|January 30, 2009
Inherited bleeding disorders: a 14-year retrospective studySuhair S Eid, Nazmi R Kamal, Taisir S Shubeilat, et al.
Human Reproduction (Oxford, England)|July 13, 2006
Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failureHussein S Qublan, Suhair S Eid, Hani A Ababneh, et al.
European Journal of Haematology|January 17, 2016
Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individualsMing Y Lim, Allison M Deal, Steven Kim, et al.
Human Mutation|October 8, 2009
Widening the mutation spectrum of EVC and EVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts Hedgehog signalingMaria Valencia, Pablo Lapunzina, Derek Lim, et al.
European Journal of Epidemiology|August 1, 2013
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controlsBenedetto Simone, Valerio De Stefano, Emanuele Leoncini, et al.
Pageof 1