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Prothrombin C20209T mutation in deep vein thrombosis: A case report
(E-Century Publishing Corporation, 2015)
Down-Syndrome associated with MBL-deficiency, IgG-deficiency, vasculitis and mutated prothrombin
(Sociedad Médica de Santiago, 2009)
Impact of screening on thrombophilia for patients with venous thrombosis
(Edizioni Minerva MedicaTurinItália, 2006)
The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis
(Lippincott Williams & WilkinsPhiladelphiaEUA, 2000)
Factor V Leiden y mutación de la protrombina G20210A en pacientes con trombosis venosa y arterial
(Sociedad Médica de Santiago, 2005)
Factor V Leiden y mutación de la protrombina G20210A en pacientes con trombosis venosa y arterialFactor V Leiden and prothrombin G20210A among Chilean patients with venous and arterial thrombosis
(Publicación del Sociedad Médica de Santiago, 2008)
Prevalence of the prothrombin gene variant 20210 G -> A among patients with myocardial infarction
(Elsevier Science BvAmsterdamHolanda, 1998)
Inherited risk factors for thrombophilia in children with nephrotic syndrome
(Springer VerlagNew YorkEUA, 1998)
Label-free oligonucleotide-based SPR biosensor for the detection of the gene mutation causing prothrombin-related thrombophilia
(MDPI, 2020)
Prothrombin-related thrombophilia is a genetic disorder produced by a substitution of a single DNA base pair, replacing guanine with adenine, and is detected mainly by polymerase chain reaction (PCR). A suitable alternative ...