Search Results - "Siqueira, Lucia H"

Longitudinal sequencing of RUNX1 familial platelet disorder: new insights into genetic mechanisms of transformation to myeloid malignancies by Duarte, Bruno K. L., Yamaguti‐Hayakawa, Gabriela G., Medina, Samuel S., Siqueira, Lúcia H., Snetsinger, Brooke, Costa, Fernando F., Rauh, Michael J., Ozelo, Margareth C.

“…Summary The mechanisms by which patients with RUNX1 familial platelet disorder with propensity to myeloid malignancies (FPDMM) develop myeloid malignancies…”
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Genetic variations in sites of affinity between FVIII and LRP1 are not associated with high FVIII levels in venous thromboembolism by Bittar, Luis F., Siqueira, Lucia H., Orsi, Fernanda A., De Paula, Erich V., Annichino-Bizzacchi, Joyce M.

“…Increased factor VIII (FVIII) levels are a prevalent and independent risk factor for venous thromboembolism (VTE). The low density lipoprotein receptor-related…”
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Paraoxonase 192 Gln→Arg polymorphism: An independent risk factor for nonfatal arterial ischemic stroke among young adults by VOETSCH, Barbara, BENKE, Kelly S, DAMASCENO, Benito P, SIQUEIRA, Lucia H, LOSCALZO, Joseph

“…The etiology of arterial ischemic stroke (AIS) in the young remains unknown in one third of patients. Serum paraoxonase (PON1) is an HDL-associated esterase…”
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Polymorphisms and mutations in vWF and ADAMTS13 genes and their correlation with plasma levels of FVIII and vWF in patients with deep venous thrombosis by Bittar, Luis Fernando, de Paula, Erich Vinícius, Mello, Tayana B T, Siqueira, Lúcia H, Orsi, Fernanda L A, Annichino-Bizzacchi, Joyce M

“…Increased levels of factor VIII (FVIII) are a prevalent and independent risk factor for deep venous thrombosis (DVT) and are affected by von Willebrand factor…”
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Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B 12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children by Aléssio, Ana C.M., Höehr, Nelci F., Siqueira, Lúcia H., Bydlowski, Sérgio P., Annichino-Bizzacchi, Joyce M.

“…One of the etiologies of hyperhomocysteinemia is decreased vitamin B 12. Genetic variation in the transcobalamin II gene, the transporter of vitamin B 12 to…”
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Low density lipoprotein receptor-related protein polymorphisms are not risk factors for venous thromboembolism by Mello, Tayana B.T, Siqueira, Lúcia H, Montavão, Silmara A.L, Ozello, Margarete C, Annichino-Bizzacchi, Joyce M

“…Abstract Low-density lipoprotein receptor-related protein is a receptor involved in factor VIII catabolism. In spite of elevated factor VIII coagulant activity…”
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Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children by Aléssio, Ana C.M, Höehr, Nelci F, Siqueira, Lúcia H, Bydlowski, Sérgio P, Annichino-Bizzacchi, Joyce M

“…Abstract One of the etiologies of hyperhomocysteinemia is decreased vitamin B12 . Genetic variation in the transcobalamin II gene, the transporter of vitamin…”
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Polymorphisms in the CBS gene and homocysteine, folate and vitamin B12 levels: Association with polymorphisms in the MTHFR and MTRR genes in Brazilian children by Aléssio, Ana C.M., Siqueira, Lúcia H., Bydlowski, Sérgio P., Höehr, Nelci F., Annichino-Bizzacchi, Joyce M.

“…Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR) and cystathionine β‐synthase (CBS) genes, involved in…”
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The protective effect of the T(−107)C promoter polymorphism of the paraoxonase gene in arterial thrombotic disease by Voetsch, Barbara, Benke, Kelly S., Damasceno, Benito P., Siqueira, Lucia H., Loscalzo, Josepho

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Acquired Hemophilia a Relapse Is Related to Th2 Response, and Increased Expression of B-Cell Activating Factor (BAFF) by Frade-Guanaes, Jessica O, Racanelli, Ana P, Siqueira, Lucia H, Costa-Lima, Carolina, Medina, Samuel S, Foschi, Nivia M, Colella, Marina P, Montalvão, Silmara A L, Yamaguti-Hayakawa, Gabriela G, Ozelo, Margareth C

“…Acquired hemophilia A (AHA) is a rare autoimmune disorder caused by the development of autoantibodies against the factor (F)VIII of coagulation with higher…”
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Genetic variability of platelet glycoprotein Ibα gene by Ozelo, Margareth C., Costa, Devanira S.P., Siqueira, Lucia H., Machado, Tania M.F., Castro, Vagner, Gonçalves, Marilda S., Menezes, Raimundo C., Soares, Manoel, Annichino‐Bizzacchi, Joyce M., Costa, Fernando F., Arruda, Valder R.

“…Platelet membrane glycoprotein (GP) Ibα is a critical component of platelet adhesion complex to subendothelium structures following tissue injury or…”
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Prevalence of factor VII deficiency and molecular characterization of the F7 gene in Brazilian patients by Rodrigues, Dalva N, Siqueira, Lucia H, Galizoni, Andréa M, Arruda, Valder R, Annichino-Bizzacchi, Joyce M

“…The prevalence of factor VII (FVII) deficiency in 267 Brazilian patients was estimated to be 4.1%, including one patient with significant bleeding, five with…”
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Longitudinal sequencing of RUNX 1 familial platelet disorder: new insights into genetic mechanisms of transformation to myeloid malignancies by Duarte, Bruno K. L., Yamaguti‐Hayakawa, Gabriela G., Medina, Samuel S., Siqueira, Lúcia H., Snetsinger, Brooke, Costa, Fernando F., Rauh, Michael J., Ozelo, Margareth C.

“…Summary The mechanisms by which patients with RUNX 1 familial platelet disorder with propensity to myeloid malignancies ( FPDMM ) develop myeloid malignancies…”
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Genetic variability of platelet glycoprotein Ibalpha gene by Ozelo, Margareth C, Costa, Devanira S P, Siqueira, Lucia H, Machado, Tania M F, Castro, Vagner, Gonçalves, Marilda S, Menezes, Raimundo C, Soares, Manoel, Annichino-Bizzacchi, Joyce M, Costa, Fernando F, Arruda, Valder R

“…Platelet membrane glycoprotein (GP) Ibalpha is a critical component of platelet adhesion complex to subendothelium structures following tissue injury or…”
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Polymorphisms in the CBS gene and homocysteine, folate and vitamin B 12 levels: Association with polymorphisms in the MTHFR and MTRR genes in Brazilian children by Aléssio, Ana C.M., Siqueira, Lúcia H., Bydlowski, Sérgio P., Höehr, Nelci F., Annichino‐Bizzacchi, Joyce M.

“…Abstract Polymorphisms in the methylenetetrahydrofolate reductase ( MTHFR ), methionine synthase reductase ( MTRR ) and cystathionine β‐synthase ( CBS ) genes,…”
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Prevalence of the mutation C677 → T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil by Arruda, Valder R., Siqueira, Lucia H., Gonçalves, Marilda S., von Zuben, Paula M., Soares, Manoel C.P., Menezes, Raimundo, Annichino-Bizzacchi, Joyce M., Costa, Fernando F.

“…Vascular disease is a serious public health problem in the industrialized world, and is a frequent cause of death among the adult population of Brazil. Mild…”
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C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction by Annichino-Bizzacchi, J M, Saad, S T, Arruda, V R, Ramires, J A, Siqueira, L H, Chiaparini, L C, Mansur, A P

“…Iron is suspected to play a role in the development of atherosclerosis and in the progression of the disease, and consequently in myocardial infarction…”
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