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Results: 1-12 |
Results: 12
C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction
Authors: Annichino-Bizzacchi, JM Saad, STO Arruda, VR Ramires, JAF Siqueira, LH Chiaparini, LC Mansur, AP
Citation: Jm. Annichino-bizzacchi et al., C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction, J CARD RISK, 7(1), 2000, pp. 37-40
The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis
Authors: Torresan, M Machado, TFGS Siqueira, LH Ozelo, MC Arruda, VR Annichino-Bizzacchi, JM
Citation: M. Torresan et al., The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis, BL COAG FIB, 11(7), 2000, pp. 679-682
The human platelet alloantigen 5 polymorphism as a risk for the development of acute idiopathic thrombocytopenia purpura
Authors: Castro, V Oliveira, GB Origa, AF Annichino-Bizzacchi, JM Arruda, VR
Citation: V. Castro et al., The human platelet alloantigen 5 polymorphism as a risk for the development of acute idiopathic thrombocytopenia purpura, THROMB HAEM, 84(2), 2000, pp. 360-361
Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults
Authors: Voetsch, B Damasceno, BP Camargo, ECS Massaro, A Bacheschi, LA Scaff, M Annichino-Bizzacchi, JM Arruda, VR
Citation: B. Voetsch et al., Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults, THROMB HAEM, 83(2), 2000, pp. 229-233
Allelic frequencies of three VNTRs in intron 40 of the human von Willebrand factor gene in types 1, 2, and 3 von Willebrand disease patients and controls of a Brazilian population
Authors: Mazzini, J Hackel, C Annichino-Bizzacchi, JM
Citation: J. Mazzini et al., Allelic frequencies of three VNTRs in intron 40 of the human von Willebrand factor gene in types 1, 2, and 3 von Willebrand disease patients and controls of a Brazilian population, THROMB RES, 100(6), 2000, pp. 489-494
Determination of the frequency of the 35delG allele in Brazilian neonates
Authors: Sartorato, EL Gottardi, E de Oliveira, CA Magna, LA Annichino-Bizzacchi, JM Seixas, CA Maciel-Guerra, AT
Citation: El. Sartorato et al., Determination of the frequency of the 35delG allele in Brazilian neonates, CLIN GENET, 58(4), 2000, pp. 339-340
Frequencies of platelet-specific alloantigen systems 1-5 in three distinctethnic groups in Brazil
Authors: Castro, V Origa, AF Annichino-Bizzacchi, JM Soares, M Menezes, RC Goncalves, MS Costa, FF Arruda, VR
Citation: V. Castro et al., Frequencies of platelet-specific alloantigen systems 1-5 in three distinctethnic groups in Brazil, EUR J IMM, 26(5), 1999, pp. 355-360
Inherited risk factors for thrombophilia among children with Legg-Calve-Perthes disease
Authors: Arruda, VR Belangero, WD Ozelo, MC Oliveira, GB Pagnano, RG Volpon, JB Annichino-Bizzacchi, JM
Citation: Vr. Arruda et al., Inherited risk factors for thrombophilia among children with Legg-Calve-Perthes disease, J PED ORTH, 19(1), 1999, pp. 84-87
Hereditary hemorrhagic telangiectasia response to aminocaproic acid treatment
Authors: Annichino-Bizzacchi, JM Facchini, RM Torresan, MZ Arruda, VR
Citation: Jm. Annichino-bizzacchi et al., Hereditary hemorrhagic telangiectasia response to aminocaproic acid treatment, THROMB RES, 96(1), 1999, pp. 73-76
A novel splice site mutation in a Brazilian patient with hereditary antithrombin deficiency type I
Authors: Arnaldi, LAT Polimeno, NC Arruda, VR Annichino-Bizzacchi, JM
Citation: Lat. Arnaldi et al., A novel splice site mutation in a Brazilian patient with hereditary antithrombin deficiency type I, HUMAN HERED, 49(2), 1999, pp. 119-120
A novel nonsense mutation 6,E-X in the protein S gene causes type I deficiency
Authors: Pugliese, L Arruda, VR Annichino-Bizzacchi, JM
Citation: L. Pugliese et al., A novel nonsense mutation 6,E-X in the protein S gene causes type I deficiency, HUMAN HERED, 49(2), 1999, pp. 121-122
Determination of the allele frequencies of three polymorphisms in the promoter region of the human protein C gene in three Brazilian ethnic groups
Authors: Mendes, CPO Hackel, C Arruda, VR Annichino-Bizzacchi, JM
Citation: Cpo. Mendes et al., Determination of the allele frequencies of three polymorphisms in the promoter region of the human protein C gene in three Brazilian ethnic groups, HUMAN HERED, 49(1), 1999, pp. 27-30
Risultati: 1-12 |