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Number of items: 8.

Meienberg, J; Rohrbach, M; Neuenschwander, S; Spanaus, K; Giunta, C; Alonso, S; Arnold, E; Henggeler, C; Regenass, S; Patrignani, A; Azzarello-Burri, S; Steiner, B; Nygren, A; Carrel, T; Steinmann, B; Matyas, G (2010). Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency. European Journal of Human Genetics, 18(12):1315-1321.

Vida, V L; Padalino, M A; Boccuzzo, G; Tarja, E; Berggren, H; Carrel, T; Ciçek, S; Crupi, G; Di Carlo, D; Di Donato, R; Fragata, J; Hazekamp, M; Hraska, V; Maruszewski, B; Metras, D; Pozzi, M; Prêtre, René; Rubay, J; Sairanen, H; Sarris, G; Schreiber, C; Meyns, B; Tlaskal, T; Urban, A; Thiene, G; Stellin, G (2010). Scimitar syndrome: a European Congenital Heart Surgeons Association (ECHSA) multicentric study. Circulation, 122(12):1159-1166.

Pilop, C; Aregger, F; Gromann, R C; Brunisholz, R; Gerrits, B; Schaffner, T; Gromann, J H; Mátyás, G; Carrel, T; Frey, Brigitte M (2009). Proteomic analysis in aortic media of patients with Marfan syndrome reveals increased activity of calpain 2 in aortic aneurysms. Circulation, 120(11):983-991.

Magyar, I; Colman, D; Arnold, E; Baumgartner, D; Bottani, A; Fokstuen, S; Addor, M C; Berger, W; Carrel, T; Steinmann, B; Mátyás, G (2009). Quantitative sequence analysis of FBN1 premature termination codons provides evidence for incomplete NMD in leukocytes. Human Mutation, 30(9):1355-1364.

Immer, F; Marti, P; Steinmann, B; Carrel, T (2008). Lebensqualität herzoperierter und nicht herzoperierter Marfan-Patienten in der Schweiz. In: Hagmann, A. Herzsache : Gesundheitskompetenz und Empowerment bei chronischen körperlichen Beeinträchtigungen am Beispiel des Marfan-Syndroms. Bern: Marfan Stiftung Schweiz, 33-41.

Mátyás, G; Alonso, S; Patrignani, A; Marti, M; Arnold, E; Magyar, I; Henggeler, C; Carrel, T; Steinmann, B; Berger, W (2007). Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome. Human Genetics, 122(1):23-32.

Matyas, G; Arnold, E; Carrel, T; Baumgartner, D; Boileau, C; Berger, W; Steinmann, B (2006). Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders. Human Mutation, 27(8):760-769.

Vogt, P R; Brunner-La Rocca, H P; Carrel, T; von Segesser, L K; Ruef, C; Debatin, J; Seifert, Burkhardt; Kiowski, W; Turina, M I (1998). Cryopreserved arterial allografts in the treatment of major vascular infection: a comparison with conventional surgical techniques. Journal of Thoracic and Cardiovascular Surgery, 116(6):965-972.

This list was generated on Tue Jul 25 01:47:27 2017 CEST.