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        Enfermedad de Huntington infantil: reporte del primer caso en Costa Rica confirmado por análisis molecular 

        Vásquez Cerdas, Melissa; Sevilla Acosta, Fabricio José; Gutiérrez Mata, Alfonso; Morales Montero, Fernando; Cuenca Berger, Patricia (2016)
        La enfermedad de Huntington (HD, por sus siglas en inglés) es una enfermedad neurodegenerativa progresiva, con una prevalencia en la población caucásica de 10.6-13.7 casos por 100 000 habitantes. La prevalencia de la ...

        Aav-mediated delivery of the transcription factor xbp1s into the striatum reduces mutant huntingtin aggregation in a mouse model of huntington?S Disease 

        Unknown author (ACADEMIC PRESS INC ELSEVIER SCIENCE, 2012)

        Aav-mediated delivery of the transcription factor xbp1s into the striatum reduces mutant huntingtin aggregation in a mouse model of huntington?S Disease 

        Unknown author (ACADEMIC PRESS INC ELSEVIER SCIENCE, 2012)

        Use of the frontal assessment battery in evaluating executive dysfunction in patients with Huntington`s disease 

        RODRIGUES, Guilherme Riccioppo; SOUZA, Carolina Pinto; CETLIN, Roberto Satler; OLIVEIRA, Daniel Sabino de; PENA-PEREIRA, Marcio; UJIKAWA, Liliana Tiemi; MARQUES JR., Wilson; TUMAS, Vitor (DR DIETRICH STEINKOPFF VERLAG, 2009)
        The frontal assessment battery (FAB) is a bedside cognitive scale designed to measure executive functions. Huntington`s disease (HD) is a neurodegenerative disorder characterized by motor, behavioral, and cognitive ...

        Clinical and genetic characteristics in patients with Huntington's Disease from Argentina 

        Gatto, Emilia Mabel; Parisi, Virginia; Persi, Gabriel; Converso, Daniela Paola; Etcheverry, José Luis; Varela, Viviana; Alba, Liliana; Fretchel, Gustavo (Elsevier, 2012-02)
        Huntington's Disease (HD) is a neurodegenerative disease, caused by the expansion of an unstable (CAG) n in the HTT gene. There is scarce data about the disease in Argentina. Objective: To describe the demographic, clinical ...

        Mv-mediated delivery of the transcription factor xbp1s into the striatum reduces mutant huntingtin aggregation in a mouse model of huntingtons disease 

        Unknown author (ACADEMIC PRESS INC ELSEVIER SCIENCE, 2012)

        Mv-mediated delivery of the transcription factor xbp1s into the striatum reduces mutant huntingtin aggregation in a mouse model of huntingtons disease 

        Unknown author (ACADEMIC PRESS INC ELSEVIER SCIENCE, 2012)

        Converging pathways in the occurrence of endoplasmic reticulum (er) stress in huntington?S Disease 

        Unknown author (BENTHAM SCIENCE PUBLISHERS, 2011)

        Increase in bax expression and apoptosis are associated in Huntington's disease progression 

        Teles, A. V. F. F. [UNIFESP]; Rosenstock, T. R. [UNIFESP]; Okuno, C. S. [UNIFESP]; Lopes, G. S. [UNIFESP]; Bertoncini, C. R. A. [UNIFESP]; Smaili, Soraya Soubhi [UNIFESP] (Elsevier B.V., 2008-06-13)
        Huntington's disease (HD) is a hereditary dominant neurodegenerative disorder and the progression of the disease may be associated with apoptosis and altered expression of apoptotic proteins. the aim of this study was to ...

        Your misery is no longer my pleasure: reduced schadenfreude in Huntington's disease families. 

        Ibáñez, Agustín
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        Red de Repositorios Latinoamericanos
        + of 4.000.000
        Available publications
        163 Participating institutions
        Dirección de Servicios de Información y Bibliotecas (SISIB)
        Universidad de Chile
        Membership Login
        Featured collections
        • Latin American Theses
        • Argentinean Theses
        • Chilean Theses
        • Peruvian Theses
        Latest collections added
        • Argentina
        • Brazil
        • Colombia
        • México
        Dirección de Servicios de Información y Bibliotecas (SISIB)
        Universidad de Chile
        Red de Repositorios Latinoamericanos | 2006-2018