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The First Homozygous Family for Prothrombin G20210A Polymorphism Reported in Latin America
(Sage PublicationsGenética Molecular (GENMOL)Grupo ReproducciónNueva York, Estados Unidos, 2022)
Long-term prospective study of recurrent venous thromboembolism in a Hispanic population
(Lippincott Williams & WilkinsPhiladelphiaEUA, 2010)
Prevalence of three prothrombotic polymorphisms: Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina
(Pergamon-elsevier Science LtdOxfordInglaterra, 2000)
Molecular analysis of homocystinuria in Brazilian patients
(Elsevier B.V., 2005-12-01)
Background: Cystathionine beta-synthase (CBS) deficiency is the most common cause of homocystinuria. However, no data are available concerning the molecular basis of this disease in Brazilian populations.Methods: We studied ...
Inherited Thrombophilia is Associated With Deep VeinThrombosis in a Colombian Population
(Wiley-BlackwellGenética Molecular (GENMOL)Grupo ReproducciónGrupo de Investigación en Ciencias Agrarias -GRICA-Grupo de Investigación en TrombosisNueva York, Estados Unidos, 2022)
Alterações genéticas em casais com antecedentes de aborto recorrente no primeiro trimestre da gestação
(Centro de Pesquisas Gonçalo Moniz, 2014)
Asociación de trombofilia con mutaciones en el gen que codifica para el factor V, la protrombina y la metiltetrahidrofolato reductasa: descripción de dos casos familiares
(2016-06-03)
Las trombofilias son alteraciones del equilibrio homeostático, esto predispone a la formación de pequeños trombos a nivel venoso y raramente en las arterias. Las trombofilias se han clasificado en hereditarias y adquiridas ...
Thrombophilic mutations and risk of retinal vein occlusion
(Conselho Brasileiro de Oftalmologia, 2007-12-01)
PURPOSE: The association of retinal vein occlusion and hereditary thrombophilia abnormalities is not established, with controversial results in the literature. This study investigates the association between retinal vein ...