Thrombophilia
Mostrando 13-24 de 37 artigos, teses e dissertações.
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13. AlteraÃÃo bioquÃmica em fator de coagulaÃÃo como causa de trombose venosa profunda â relato de caso clÃnico
Deep venous thrombosis (DVT) in the pediatric population (0-18 year old) has been reported as lower than in adults. In almost half of the children, three or four risk factors for thrombosis are present simultaneously. Even in children with thromboembolic disturbance, thrombosis did not occur spontaneously; the hemostatic defect became apparent because thromb
Publicado em: 2006
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14. Impact of the laboratory screening on thrombophilia for the secondary prevention and management of the patients with venous thromboembolism / Impacto da pesquisa laboratorial de trombofilia na prevençao secundaria e orientação dos doentes com troboembolismo venoso
O tromboembolismo venoso (TEV) afeta de 1 a 3 indivíduos por mil habitantes/ano. O conhecimento atual das trombofilias permite a associação com cerca de 40% dos casos de TEV. Há controvérsias quanto ao valor da pesquisa laboratorial de trombofilia para o benefício dos doentes com tromboembolismo venoso. Procuraram-se as variáveis preditivas para a pes
Publicado em: 2006
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15. Prevalence of hereditary risk factors for thrombophilia in Belém, Brazilian Amazon
Different risk factors for venous thromboembolism (VTE) have been identified, including hereditary abnormalities in the mechanisms of coagulation and fibrinolysis. We investigated five genetic polymorphisms (FVL G1691A, FII G20210A, MTHFR C677T, TAFI A152G and TAFI T1053C) associated with VTE in individuals from the city of Belém in the Brazilian Amazon who
Genetics and Molecular Biology. Publicado em: 2006
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16. DetecÃÃo do fator V Leiden em pacientes trombofÃlicos no Estado do CearÃ. / Detection of factor V Leiden in patients with thrombophilia in CearÃ, Brazil
As doenÃas trombÃticas constituem um sÃrio problema na saÃde mundial. Diversas desordens hereditÃrias, que afetam o sistema fisiolÃgico anticoagulante, estÃo atualmente estabelecidas como fatores de risco para a ocorrÃncia do evento trombÃtico. Dentre estes o fator V Leiden à o mais freqÃente. A associaÃÃo entre alteraÃÃes no gene do fator V e
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 06/08/2004
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17. Defeito bioquÃmico em fator V, fator V de Leiden, em paciente jovem com trombose venosa profunda: estudo de caso
Inherited disturbances of the coagulation and fibrinolysis have been associated with thrombophilia. Trauma can be a precipitant of the deep vein thrombosis (DVT) in Factor V Leiden (FVL) carriers, the most common polymorphism cause of hereditary thrombophilia. The objective of this study was to analyze the case of a 15 years old boy, his parents and a contro
Publicado em: 2001
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18. Thrombophilia and pregnancy
Pregnancy is hypercoagulable state. The field of thrombophilia; the tendency to thrombosis, has been developed rapidly and has been linked to many aspects of pregnancy. It is recently that severe pregnancy complications such as severe preeclampsia intrauterine growth retardation abruptio placentae and stillbirth has been shown to be associated with thromboph
BioMed Central.
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19. Case Reports: Heritable Thrombophilia Associated with Deep Venous Thrombosis after Shoulder Arthroscopy
Thromboembolic complications after shoulder arthroscopy are rare and their cause has not been well determined. Heritable thrombophilia has been studied in relation to numerous clinical conditions, and it has been associated with thromboembolic complications after some orthopaedic surgeries, especially after total hip or knee arthroplasty. We report three pat
Springer-Verlag.
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20. The role of d-dimer as first marker of thrombophilia in women affected by sterility: implications in pathophysiology and diagnosis of thrombophilia induced sterility
BioMed Central.
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21. An assessment of the comparative utility of functional and molecular level analyses in the investigation of patients with thrombophilia
Aim—To determine the relation of the low anticoagulant response phenotype with the Factor V Q506 (Leiden) mutation in a cohort of patients with thrombophilia.
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22. Markers of thrombin and plasmin generation in patients with inherited thrombophilia.
AIM--To determine the prevalence of a biochemically detectable hypercoagulable state, defined in terms of increased thrombin or plasmin generation, in patients with phenotypically characterised thrombophilia. METHODS--Plasma concentrations of the prothrombin activation peptide F1.2 and fibrin degradation (FbDP) and fibrinogen degradation products (FgDP) were
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23. Celiac artery embolism due to thrombophilia – a case report
A case of celiac artery embolism in a patient with factor V Leiden thrombophilia is reported. The embolism was likely due to an undetected cardiac thrombus, causing an abdominal aortic embolism. The patient underwent emergency surgery for the abdominal embolism. The celiac artery embolism was treated nonsurgically due to the presence of collateral circulatio
Pulsus Group Inc.
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24. Inherited thrombophilia and pregnancy associated venous thromboembolism
BMJ Publishing Group Ltd..