Browsing by Author "28c22c8f-9bbe-493d-a383-fbf900904038"
Now showing items 1-6 of 6
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Torres, Mauricio; Cartier Rovirosa, Luis; Matamala, José Manuel; Hernández, Nancy; Woehlbier, Ute; Hetz Flores, Claudio (2012)Creutzfeldt-Jakob disease (CJD) is the most frequent human Prion-related disorder (PrD). The detection of 14-3-3 protein in the cerebrospinal fluid (CSF) is used as a molecular diagnostic criterion for patients clinically ...
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Moreno, Jenny; Lara, Alejandro; Torres, Mauricio (Elsevier Ltd, 2019)This paper examines the role of community resilience during the emergency response after the 2010 Chile earthquake and tsunami. El Morro – a fishing community that managed to survive the tsunami in the Talcahuano region – ...
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Torres, Mauricio; Matamala, José Manuel; Durán Aniotz, Claudia; Cornejo, Víctor Hugo; Foley, Andrew; Hetz Flores, Claudio (Elsevier, 2015)© 2014 Elsevier B.V. Alzheimer's and Prion diseases are two neurodegenerative conditions sharing different pathophysiological characteristics. Disease symptoms are associated with the abnormal accumulation of protein ...
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Burgos, Pablo I.; Lara, Oriana; Lavado, Alejandro; Rojas Sepúlveda, Ignacia; Delgado D., Carolina; Bravo, Eusebio; Kamisato, Cristian; Torres Elgueta, Julio; Castañeda, Víctor; Cerda, Mauricio (MDPI, 2020)Stroke is currently the world's second cause of disability. It can cause deficits such as postural control, and telerehabilitation could improve the therapeutic dose as well as functional results. The aim of this work is ...
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Lévican, Jorge; Torres, Mauricio; Gaggero, Nicolás; Corvalán, Rosa; Gaggero Brillouet, Aldo (2011)Background: Parvovirus B19 (B19) is associated with a wide range of diseases in humans, whose severity depends on the immunological and hematological status of the host. It is transmitted mainly through the airway but also ...
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Torres, Mauricio; Castillo, Karen; Armisen Yáñez, Ricardo; Stutzin Schottlander, Andrés; Soto, Claudio; Hetz Flores, Claudio (2010)Prion-related disorders (PrDs) are fatal neurodegenerative disorders characterized by progressive neuronal impairment as well as the accumulation of an abnormally folded and protease resistant form of the cellular prion ...