Welcome to the UPF Digital Repository

The institutional repository collects, disseminates and preserves, in digital form, the intellectual output that results from the academic and research activity of the UPF and also the scientific magazines and the institutional publications. Its purpose is to increase the impact of research done at the UPF and its intellectual memory.

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Recently Added

  • Zimmer, Veronika Anne; Glocker, Ben; Hahner, Nadine; Eixarch, Elisenda; Sanromà, Gerard; Gratacós Solsona, Eduard; Rueckert, Daniel; González Ballester, Miguel Ángel, 1973-; Piella Fenoy, Gemma (Elsevier, 2017)
    It is challenging to characterize and classify normal and abnormal brain development during early childhood. To reduce the complexity of heterogeneous data population, manifold learning techniques are increasingly applied, ...
  • Garcia-Canadilla, Patricia; Rodriguez, Jose F.; Palazzi, Maria J.; Gonzalez-Tendero, Anna; Schönleitner, Patrick; Balicevic, Vedrana; Loncaric, Sven; Luiken, Joost J. F. P.; Ceresa, Mario; Camara, Oscar; Antoons, Gudrun; Crispi, Fatima; Gratacos, Eduard; Bijnens, Bart (Public Library of Science (PLoS), 2017)
    Experimental studies on isolated cardiomyocytes from different animal species and human hearts have demonstrated that there are regional differences in the Ca2+ release, Ca2+ decay and sarcomere deformation. Local deformation ...
  • Mas‐Stachurska, Aleksandra; Siegert, Anna‐Maria; Batlle, Monsterrat; Gorbenko del Blanco, Darya; Meirelles, Thayna; Rubies, Cira; Bonorino, Fabio; Serra‐Peinado, Carla; Bijnens, Bart; Baudin, Julio; Sitges, Marta; Mont, Lluís; Guasch, Eduard; Egea, Gustavo (Wiley, 2017)
    Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy ...
  • Loncaric, Filip; Bijnens, Bart; Sitges, Marta (Bloomsbury Qatar Foundation Journals, 2018)
    Hypertrophic cardiomyopathy is clinically defined by the presence of increased left ventricular (LV) wall thickness that is not solely explained by abnormal loading conditions. The aetiology is diverse, but in 60% of ...
  • López-Guimet, Júlia; Peña-Pérez, Lucía; Bradley, Robert S.; García-Canadilla, Patricia; Disney, Catherine; Geng, Hua; Bodey, Andrew J.; Withers, Philip J.; Bijnens, Bart; Sherratt, Michael J.; Egea, Gustavo (UNLISTED PUBLISHER, 2018)
    Aortic wall remodelling is a key feature of both ageing and genetic connective tissue diseases, which are associated with vasculopathies such as Marfan syndrome (MFS). Although the aorta is a 3D structure, little attention ...

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