نتایج جستجو برای: combined factor v

تعداد نتایج: 1460603  

Journal: :Japanese Journal of Thrombosis and Hemostasis 1997

Journal: :reports of biochemistry and molecular biology 0
fatemeh keify pardis clinical and genetics laboratory, mashhad, iran. mohsen azimi-nezhad pardis clinical and genetics laboratory, mashhad, iran - department of medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran - université de lorraine, unité de recherche “interactions gène-environnement en physiopathologie cardio vasculaire” l’umr inserm u 1122, ige-pcv, nancy, france. narges zhiyan-abed pardis clinical and genetics laboratory, mashhad, iran - razavi’s social welfare organization, mashhad, iran. mojila nasseri pardis clinical and genetics laboratory, mashhad, iran. mohammad reza abbaszadegan tel: +98 5117112343; fax: +98 5117112343

background: thrombophilia is a main predisposition to thrombosis due to a procoagulant state. several point mutations play key roles in blood-clotting disorders, which are grouped under the term thrombophilia. these thrombophilic mutations are methylenetetrahydrofolate reductase (mthfr, c677t, and a1298c), factor v leiden (g1691a), prothrombin gene mutation (factor ii, g20210a), and plasminogen...

Journal: :Haematologica 2004
Elena M Faioni Giancarlo Castaman Daniela Asti Federico Lussana Francesco Rodeghiero

BACKGROUND AND OBJECTIVES Factor V HR2 possesses decreased co-factor activity to activated protein C and an increased ratio of factor V1 to factor V2. Factor V HR2 is associated with a mild increase in the risk of venous thromboembolism although not all studies concur on this point. DESIGN AND METHODS Inconsistencies in results of the epidemiological studies may stem from a failure to identif...

Journal: :Journal of clinical pathology 1960
A J QUICK

Human oxalated plasma stored at 4 degrees C. until the prothrombin time is increased beyond 60 sec. is a reliable medium for assaying labile factor (factor V) because its response to added labile factor corresponds quantitatively to that of plasma from patients with congenital deficiency of this factor. Such an agreement is not obtained with plasma stored at 37 degrees C. The stability of labil...

Journal: :Clinical chemistry 2008
Michael T Seipp David Pattison Jacob D Durtschi Mohamed Jama Karl V Voelkerding Carl T Wittwer

BACKGROUND Multiplexed amplicon melting is a closed-tube method for genotyping that does not require probes, real-time analysis, asymmetric PCR, or allele-specific PCR; however, correct differentiation of homozygous mutant and wild-type samples by melting temperature (T(m)) analysis requires high-resolution melting analysis and controlled reaction conditions. METHODS We designed 4 amplicons b...

Journal: :CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2002
Dena Bloomenthal Peter von Dadelszen Robert Liston Laura Magee Peter Tsang

Factor V Leiden is a common genetic mutation that predisposes its carriers to venous thromboembolism. When combined with the hypercoagulable state that is characteristic of pregnancy, there is an increased risk of severe and recurrent pregnancy complications. Factor V Leiden is the most common cause of primary and recurrent venous thromboembolism in pregnancy. Factor V Leiden carriage has consi...

Journal: :Blood 2004
Jeanet M Kemmeren Ale Algra Joost C M Meijers Guido Tans Bonno N Bouma Joyce Curvers Jan Rosing Diederick E Grobbee

A plausible mechanism to explain thrombotic risk differences associated with the use of second- and third-generation oral contraceptives (OCs), particularly in carriers of factor V(Leiden), is still lacking. In a double-blind trial, 51 women without and 35 women with factor V(Leiden) were randomized to either a second- (30 microg ethinylestradiol/150 microg levonorgestrel) or third- (30 microg ...

Journal: :acta medica iranica 0
hossein ali ghlichnia department of neurology, faculty of medicine, tehran university of medical sciences, tehran, iran. and department of neurogenetics, iranian center of neurological research, tehran, iran. abolghasem kollaee department of neurogenetics, iranian center of neurological research, tehran, iran. and department of medical genetics, faculty of medicine, tehran university of medical sciences, tehran, iran. majid gaffarpoor department of neurogenetics, iranian center of neurological research, tehran, iran. abolfazl movafagh department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. babak ghlichnia department of neurogenetics, iranian center of neurological research, tehran, iran. mahdi zamani department of neurogenetics, iranian center of neurological research, tehran, iran. and department of medical genetics, faculty of medicine, tehran university of medical sciences, tehran, iran.

multiple sclerosis (ms) is an inflammatory demyelinating disease of the central nervous system. it is a clinically heterogeneous disorder especially in terms of disease severity. current investigations suggest that genes and gene-gene interactions not only influence on susceptibility to ms but also affect the disease severity. in this study, we investigated the contribution of the hladrb1*1501 ...

2004
Muriel Giansily-Blaizot Gilbert Tchernia

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید