G.T.SucakandZ.AkiSDOSCanadian Journal of Ophthalmology / Journal Canadien d'OphtalmologieSucak GT, Aki Z, Or M. Protein S deficiency with homozygous factor V Leiden mutation in central retinal vein occlusion. Can J Ophthalmol 2007;42:632-3.
Factor V Leiden易栓症是一种儿科疾病。佳学基因对Factor V Leiden易栓症的发生进行了基因解码,并将之收入《人的基因序列变化与人体疾病表征》中,便于医生选择和使用,进行Factor V Leiden易栓症遗传阻断,也便于患者更好地进行治疗和健康管理。 Factor V Leiden易栓症疾病介绍: Factor V Leiden易栓症是一种遗传性...
All mutations are believed to interfere with protein S binding to C4b-binding protein resulting in reduced free protein S levels. Of the five individuals studied who had experienced thrombotic events, three had combined protein S deficiency and FV Leiden reemphasising the importance of FV Leiden as...
Browse Nearby Words factor VIII factor V Leiden factor X See all Nearby Words Cite this Entry Style “Factor V Leiden.” Merriam-Webster.com Medical Dictionary, Merriam-Webster, https://www.merriam-webster.com/medical/factor%20V%20Leiden. Accessed 14 May. 2025. Copy Citation ...
FactorVLeiden易栓症是英文factor V Leiden thrombophilia的中文翻译。这一疾病又叫做facio-scapulo-humeral dystrophy facioscapulohumeral atrophy facioscapulohumeral type progressive muscular dystrophy facioscapuloperoneal muscular dystrophy FSH muscular dystrophy FSHD muscular dystrophy, facioscapulohumeral;。该病是...
The clinical expression of Factor V Leiden is influenced by the number of Factor V Leiden alleles, coexisting genetic and acquired thrombophilic disorders, and circum- stantial risk factors. Diagnosis requires the activated Protein C resis- tance assay (a coagulation screening test) or DNA analysis ...
newborn screening, or individuals taking an oral contraceptive [2]. A negative result of this test does not rule out inherited thrombophilia. Other than factor V Leiden, variants in the genes that encode coagulation factor II, protein C, protein S, and antithrombin can also cause inherited thro...
Analytic validity of genetic tests to identify Factor V Leiden and prothrombin G20210A. Am J Hematol 2010; 85:264 -270.Emadi A, Crim M, Brotman D, et al. Analytic validity of genetic tests to identify factor V leiden and prothrombin G20210A. Am J Hematol, in press....
protein C or protein S deficiency, homozygous factor V Leiden or prothrombin G20210A mutation, antiphospholipid antibodies and combined abnormalities (good prac... K Einh?Upl,MG Bousser,SFTMD Bruijn,... - 《European Journal of Neurology》 被引量: 1198发表: 2010年 Co-inheritance of the 2021...
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