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Volumn 122, Issue 14, 2004, Pages 556-557

Prevalence of thrombotic polymorphisms in the healthy population in Southern Spain [2];Prevalencia de los polimorfismos genéticos asociados a trombofilia en población sana del Sur de España

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN;

EID: 3343012321     PISSN: 00257753     EISSN: None     Source Type: Journal    
DOI: 10.1157/13060476     Document Type: Letter
Times cited : (2)

References (11)
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    • Genetic approach to thrombophilia
    • Bertina RM. Genetic approach to thrombophilia. Thromb Haemost 2001;86:92-103.
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    • Reducción de concentraciones elevadas de homocisteína con ácido fólico y vitaminas B en pacientes con tromboembolia venosa: Relación entre respuesta y genotipo C677T de la metilén tetrahidrofólico reductasa (MTHFR)
    • González Ordóñez AJ, Medina Rodríguez JM, Fernández Alvarez C, Sánchez García J, Fernández Carreira JM, Álvarez Martínez MV, et al. Reducción de concentraciones elevadas de homocisteína con ácido fólico y vitaminas B en pacientes con tromboembolia venosa: relación entre respuesta y genotipo C677T de la metilén tetrahidrofólico reductasa (MTHFR). Med Clin (Barc) 2000;114:7-12.
    • (2000) Med Clin (Barc) , vol.114 , pp. 7-12
    • González Ordóñez, A.J.1    Medina Rodríguez, J.M.2    Fernández Alvarez, C.3    Sánchez García, J.4    Fernández Carreira, J.M.5    Álvarez Martínez, M.V.6
  • 5
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    • Genetic heterogeneity in hereditary thrombophilia
    • Reitsma PH. Genetic heterogeneity in hereditary thrombophilia. Haemostasis 2000;30(Suppl 2): 1-10.
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    • Reitsma, P.H.1
  • 7
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    • Screening for inherited thrombophilia: Indications and therapeutic implications
    • Stefano V, Rossi E, Pacaroni K, Leone G. Screening for inherited thrombophilia: Indications and therapeutic implications. Haematologica 2002;87:1095-108.
    • (2002) Haematologica , vol.87 , pp. 1095-1108
    • Stefano, V.1    Rossi, E.2    Pacaroni, K.3    Leone, G.4
  • 8
    • 0034798859 scopus 로고    scopus 로고
    • Prevalence of the methylenetetrahydrofolate reductase 677C> T mutation in the Mediterranean Spanish population. Association with cardiovascular risk factor
    • Guillén M, Corella D, Portoles O, González JI, Mulet F, Saiz C. Prevalence of the methylenetetrahydrofolate reductase 677C> T mutation in the Mediterranean Spanish population. Association with cardiovascular risk factor. Eur J Epidemiol 2001;17:255-61.
    • (2001) Eur J Epidemiol , vol.17 , pp. 255-261
    • Guillén, M.1    Corella, D.2    Portoles, O.3    González, J.I.4    Mulet, F.5    Saiz, C.6
  • 9
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    • MTHFR gene polymorphism, homocysteine and cardiovascular disease
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  • 10
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    • Hyperhomocysteinemia and other inherited prothrombotic conditions in young adults with a history of ischemic stroke
    • Madonna P, De Stefano V, Coppola A, Cirillo F, Cerbone AM, Orefice G, et al. Hyperhomocysteinemia and other inherited prothrombotic conditions in young adults with a history of ischemic stroke. Stroke 2002;33:51-6.
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    • Mutations in the genes regulating methylene tetrahydrofolate reductase (MTHFR c → T677) and cystathione beta-synthase (CBS G → A919, CBS T ↑ c833) are not associated with myocradial infarction in African Americans
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.