Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy Ausência de associação entre o polimorfismo G20210A (rs1799963) da protrombina e epilepsia mioclônica juvenil

نویسندگان

  • João Paulo Lopes Born
  • Bruna Priscila dos Santos
  • Rodrigo Secolin
  • Fernando Tenório
  • Lívia Leite Góes Gitaí
  • Daniel Leite Góes Gitaí
چکیده

Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy Ausência de associação entre o polimorfismo G20210A (rs1799963) da protrombina e epilepsia mioclônica juvenil João Paulo Lopes Born1, Bruna Priscila dos Santos1, Rodrigo Secolin2, Fernando Tenório Gameleira3, Tiago Gomes de Andrade3, Luciana Cláudia Herculano Machado4, Lívia Leite Góes Gitaí5, Daniel Leite Góes Gitaí6

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Juvenile myoclonic epilepsy mimicking focal epilepsy Epilepsia mioclônica juvenil imitando epilepsia focal

1Neurology Resident at Santa Marcelina Hospital, São Paulo SP, Brazil; 2Neurologist at Santa Marcelina Hospital, São Paulo SP, Brazil. Correspondence: Valmir Passarelli; Rua Oscar Freire 1.380 / apto. 51; 05409-010 São Paulo SP Brasil; E-mail: [email protected] Conflict of interest: There is no conflict of interest to declare. Received 15 January 2012; Received in final form 27 April 2012; Ac...

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Multilocus Genetic Risk Scores for Venous Thromboembolism Risk Assessment

BACKGROUND Genetics plays an important role in venous thromboembolism (VTE). Factor V Leiden (FVL or rs6025) and prothrombin gene G20210A (PT or rs1799963) are the genetic variants currently tested for VTE risk assessment. We hypothesized that primary VTE risk assessment can be improved by using genetic risk scores with more genetic markers than just FVL-rs6025 and prothrombin gene PT-rs1799963...

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Schizophrenia is a severe psychotic disorder with recurrent relapse and functional impairment. It results from a poorly understood geneenvironment interaction. The Taq1A polymorphism (located in the gene cluster NTAD) is a likely candidate for schizophrenia. Its rs1800497 polymorphism was shown to be associated with DRD2 gene expression. Therefore the present work aims to investigate a possible...

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تاریخ انتشار 2015