dc.creator | Andrade F.L. | |
dc.creator | Annichino-Bizzacchi J.M. | |
dc.creator | Saad S.T.O. | |
dc.creator | Costa F.F. | |
dc.creator | Arruda V.R. | |
dc.date | 1998 | |
dc.date | 2015-06-30T15:05:32Z | |
dc.date | 2015-11-26T15:13:28Z | |
dc.date | 2015-06-30T15:05:32Z | |
dc.date | 2015-11-26T15:13:28Z | |
dc.date.accessioned | 2018-03-28T22:23:35Z | |
dc.date.available | 2018-03-28T22:23:35Z | |
dc.identifier | | |
dc.identifier | American Journal Of Hematology. , v. 59, n. 1, p. 46 - 50, 1998. | |
dc.identifier | 3618609 | |
dc.identifier | 10.1002/(SICI)1096-8652(199809)59:1<46::AID-AJH9>3.0.CO;2-# | |
dc.identifier | http://www.scopus.com/inward/record.url?eid=2-s2.0-0031825212&partnerID=40&md5=b5c48463bd90a9b79bb93c3aaa8bc15e | |
dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/100567 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/100567 | |
dc.identifier | 2-s2.0-0031825212 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1258648 | |
dc.description | The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homozygosity for transition 677C→T in the methylenetetrahydrofolate reductase (MTHFR) gene was determined among patients with sickle cell disease (SCD). The group included 73 patients with median age of 32,3 years with a diagnosis of sickle cell anemia in 53 patients, hemoglobinopathy SC in 16 patients, and four with S/β°thalassemia. Vascular complications such as ischemic stroke or deep vein thrombosis were diagnosed in nine patients. Heterozygosity for the prothrombin gene variant or factor V Leiden mutation was identified in four patients. However, only one patient, who developed ischemic stroke, was identified as a carrier of factor V Leiden mutation. None of the patients presented homozygosity for the thermolabile variant of the MTHFR. These data suggest a low clinical impact of inherited hypercoagulability risk factors in developing thrombosis, occlusive stroke, or mortality data among patients with SCD in Brazil. | |
dc.description | 59 | |
dc.description | 1 | |
dc.description | 46 | |
dc.description | 50 | |
dc.description | Sergeant, G.R., The painful crisis (1992) Sickle Cell Disease, p. 245. , Sergeant GR (ed): New York: Oxford University Press | |
dc.description | Francis, R.B., Platelet coagulation and fibrinolysis in sickle cell disease: Their possible role in vascular occlusion (1992) Blood Coagul Fibrinolysis, 2, p. 341 | |
dc.description | Francis, R.B., Hebbel, R.P., Hemostasis (1994) Sickle Cell Disease, p. 299. , Embury SH, Hebbel RP, Mohandas N, Steinberg MH (eds): New York: Raven Press, Ltd | |
dc.description | Hagger, D., Wolff, S., Owen, J., Samson, D., Changes in coagulation and fibrinolysis in patients with sickle cell disease compared with healthy black controls (1995) Blood Coagul Fibrinolysis, 2, p. 93 | |
dc.description | Nsiri, B., Gritli, N., Bayoudh, F., Messaoud, T., Fattoum, S., Machghoudl, Abnormalities of coagulation and fibrinolysis in homozygous sickle cell disease (1996) Hematol Cell Ther, 38, p. 279 | |
dc.description | Wright, J.G., Cooper, P., Malia, R.G., Kulozik, A.E., Vetter, B., Thomaz, P., Preston, F.E., Serjeant, G.R., Activated protein C resistance in homozygous sickle cell disease (1997) Br J Haematol, 96, p. 854 | |
dc.description | Wright, J.G., Malia, R., Cooper, P., Thomas, P., Preston, F.E., Serjeant, G.R., Protein C and protein S in homozygous sickle cell disease: Does hepatic dysfunction contribute to low levels? (1997) Br J Haematol, 98, p. 627 | |
dc.description | Tam, D.A., Protein C and protein S activity in sickle cell disease and stroke (1997) J Child Neurol, 12, p. 19 | |
dc.description | Thomaz, A.N., Pattison, C., Serjeant, G.R., Causes of death in sickle cell disease in Jamaica (1982) Br Med J, 285, p. 633 | |
dc.description | Platt, O.S., Brambilla, D.J., Rosse, W.F., Milner, P.F., Castro, O., Steinberg, M.H., Klug, P.P., Mortality in sickle cell disease (1994) N Engl J Med, 330, p. 1639 | |
dc.description | Vichinsky, E.P., Styles, L.A., Colangelo, L.H., Wright, E.C., Castro, O., Nickerson, B., Acute chest syndrome in sickle cell disease: Clinical presentation and course (1997) Blood, 89, p. 1787 | |
dc.description | Powards, D., Wilson, B., Imbus, C., Pagalow, C., Allen, J., The natural history of stroke in sickle cell anemia (1978) Am J Med, 65, p. 461 | |
dc.description | Rottman, S.M., Fulling, K.H., Nelson, J.S., Sickle cell anemia and central nervous system infarction: A neuropathological study (1986) Ann Neurol, 20, p. 684 | |
dc.description | Chaplin, H., Monroe, M.C., Malecek, A.C., Morgan, L.K., Michael, J., Murphy, W.A., Preliminary trial of minidose heparin prophylaxis for painful sickle cell crises (1989) East Afr Med J, 66, p. 574 | |
dc.description | Wolters, H.J., Ten Cate, H., Thomas, L.L.M., Brandjes, D.P.M., Van Der Ende, A., Van Der Heiden, Y., Statius Van Eps, L.W., Low intensity oral anticoagulation in sickle cell disease reverses the prethrombotic state: Promises for treatment? (1995) Br J Haematol, 90, p. 715 | |
dc.description | Dahlbäck, B., Carlsson, M., Svensson, P.J., Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C (1993) Proc Natl Acad Sci USA, 90, p. 1004 | |
dc.description | Bertina, R.M., Koeleman, B.P.C., Koster, T., Rosendaal, F.R., Dirven, R.J., Ronde, H., Van Der Velden, P.A., Reitsma, P.H., Mutation in blood coagulation factor V associated with resistance to activated protein C (1994) Nature, 369, p. 64 | |
dc.description | De Stefano, V., Finazzi, G., Mannucci, P.M., Inherited thrombophilia: Pathogenesis, clinical syndromes, and management (1996) Blood, 87, p. 3531 | |
dc.description | Lane, D.A., Mannucci, P.M., Bauer, K.A., Bertina, R.M., Bochkov, N.P., Boulyjenkov, V., Chandy, M., Selingsohn, U., Inherited thrombophilia: Part I (1996) Thromb Haemostasis, 76, p. 651 | |
dc.description | Poort, S.R., Rosendaal, F.R., Reitsma, P.H., Bertina, R.M., A common genetic variant in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis (1996) Blood, 88, p. 3698 | |
dc.description | Ross, R., Pathogenesis of atherosclerosis (1994) Hemostasis and Thrombosis: Basic Principles and Clinical Practice, p. 861. , Colman RW, Hirsh J, Marder VJ, Salzman EW, (eds): Philadelphia: J.B. Lippincott Company | |
dc.description | Simioni, P., Zanardi, S., Saracino, A., Girolami, A., Occurrence of arterial thrombosis in a cohort of patients with hereditary deficiency of clotting inhibitors (1992) J Med, 23, p. 61 | |
dc.description | Boers, G.H.J., Smals, A.G.H., Trijbels, F.J.M., Fowler, B., Bakkeren, J.A.J.M., Schoonderwaldt, H.C., Kleijer, W.J., Kloppenborg, P.W.C., Heterozygosity for homocystinuria in peripheral and cerebral occlusive arterial disease (1985) N Engl J Med, 313, p. 709 | |
dc.description | Clarke, R., Daly, L., Robinson, K., Naughten, E., Cahalane, S., Fowler, B., Graham, I., Hyperhomocysteinemia: An independent risk factor for vascular disease (1991) N Engl J Med, 324, p. 1149 | |
dc.description | Kang, S.S., Wong, P.W.K., Zhou, J., Sora, J., Lessick, M., Ruggie, N., Thermolabile methylenetetrahydrofolate reductase in patients with coronary artery disease (1988) Metabolism, 37, p. 611 | |
dc.description | Froost, P., Blom, H.J., Milos, R., Goyette, P., Sheppard, C.A., Matthews, R.G., Boers, G.H.J., Rozen, R., A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase (1995) Nat Genet, 10, p. 111 | |
dc.description | Arruda, V.R., Von Zuben, P.M., Chiaparini, L.C., Annichino-Bizzacchi, J.M., Costa, F.F., The mutation Ala677→Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis (1997) Thromb Haemost, 77, p. 818 | |
dc.description | Arruda, V.R., Annichino-Bizzacchi, J.M., Costa, F.F., Reitsma, P.H., Factor V Leiden (FVQ506) is common in Brazilian population (1995) Am J Hematol, 39, p. 242 | |
dc.description | Arruda, V.R., Annichino-Bizzachi, J.M., Gonçalves, M.S., Costa, F.F., Prevalence of the prothrombin gene variant (20210A) in venous thrombosis and arterial disease (1997) Thromb Haemost, 78, pp. 1430-1433 | |
dc.description | Figueiredo, M.S., Kerbauy, J., Gonçalves, M.S., Arruda, V.R., Saad, S.T.O., Sonati, M.F., Stoming, T., Costa, F.F., Effect of α-thalassemia and β-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in Brazil (1996) Am J Hematol, 53, p. 72 | |
dc.description | Millar, S.A., Dykes, D.D., Polesky, H.F., A simple salting out procedure for extracting DNA from nucleated cell (1988) Nucleic Acids Res, 16, p. 1215 | |
dc.description | Olivieri, O., Friso, S., Manzato, F., Guella, A., Bernardi, F., Lunghi, B., Girelli, D., Corrocher, R., Resistance to activated protein C in healthy women taking oral contraceptives (1995) Br J Haematol, 91, p. 465 | |
dc.description | Bokarewa, M.I., Bremme, K., Blombäck, M., Arg506→Gln mutation in factor V and risk of thrombosis during pregnancy (1996) Br J Haematol, 92, p. 473 | |
dc.description | Rees, D.S., Cox, M., Clegg, J.B., World distribution of factor V Leiden (1995) Lancet, 346, p. 1133 | |
dc.description | Motulsky, A.G., Nutritional ecogenetics: Homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid (1996) Am J Hum Genet, 58, p. 17 | |
dc.description | Arruda, V.R., Von Zuben, P.M., Soares, M.C.P., Menezes, R., Annichino-Bizzacchi, J.M., Costa, F.F., Very low incidence of Arg506→Gln mutation in the factor V gene among the Amazonian Indians and the Brazilian black population (1996) Thromb Haemost, 75, p. 860 | |
dc.description | Kahn, M.J., Scher, C., Rozans, M., Michaelis, R.K., Leissinger, C., Krause, J., Factor V Leiden is not responsible for stroke in patients with sickling disorders and is uncommon in African Americans with sickle cell disease (1997) Am J Hematol, 54, p. 12 | |
dc.description | Kontula, K., Ylikorkala, A., Miettinen, H., Vuorio, A., Kauppinen-Mäkelin, R., Hämäläinen, L., Palomäki, H., Kaste, M., Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction (1995) Thromb Haemost, 73, p. 558 | |
dc.description | Ridker, P.M., Hennekens, C.H., Lindpaintner, K., Stampfer, M.J., Eisenberg, P.R., Miletich, J.P., Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men (1995) N Engl J Med, 332, p. 912 | |
dc.description | Fisher, M., Fernández, J.A., Ameriso, S.F., Xie, D., Gruber, A., Paganini-Hill, A., Griffin, J.H., Activated protein C resistence in ischemic stroke not due to factor V argininé→glutamine mutation (1996) Stroke, 27, p. 1163 | |
dc.description | Houston, P.E., Rana, S., Sekhsaria, S., Perlin, E., Kim, K.S., Castro, O.L., Homocysteine in sickle cell disease: Relationship to stroke (1997) Am J Med, 103, p. 192 | |
dc.description | Glueck, C.J., Crawford, A., Roy, D., Freiberg, R., Glueck, H., Stroop, D., Association of antithrombotic factor deficiencies and hypofibrinolysis with Legg-Perthes disease (1996) J Bone Jt Surg, 78 A, p. 3 | |
dc.description | Glueck, C.J., Freiberg, R., Glueck, H.I., Henderson, C., Welch, M., Tracy, T., Stroop, D., Levy, M., Hypofibrinolysis: A common major cause of osteonecrosis (1994) Am J Hematol, 45, p. 156 | |
dc.language | en | |
dc.publisher | | |
dc.relation | American Journal of Hematology | |
dc.rights | fechado | |
dc.source | Scopus | |
dc.title | Prothrombin Mutant, Factor V Leiden, And Thermolabile Variant Of Methylenetetrahidrofolate Reductase Among Patients With Sickle Cell Disease In Brazil | |
dc.type | Artículos de revistas | |