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Gabor Matyas

Showing results (11-20 of 22) with videos related to

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Circulation|March 16, 2013
Acute aortic dissection determines the fate of initially untreated aortic segments in Marfan syndromeFlorian S Schoenhoff, Silvan Jungi, Martin Czerny, et al.
Current Cardiology Reviews|February 18, 2014
Medical treatment of aortic aneurysms in Marfan syndrome and other heritable conditionsChristine H Attenhofer Jost, Matthias Greutmann, Heidi M Connolly, et al.
Circulation|September 2, 2009
Proteomic analysis in aortic media of patients with Marfan syndrome reveals increased activity of calpain 2 in aortic aneurysmsChristiane Pilop, Fabienne Aregger, Robert C Gorman, et al.
Respiratory Research|January 16, 2007
Glutathione S-transferase genotypes modify lung function decline in the general population: SAPALDIA cohort studyMedea Imboden, Sara H Downs, Oliver Senn, et al.
Swiss Medical Weekly|April 4, 2020
Marfan syndrome and related connective tissue disorders in the current era in Switzerland in 103 patients: medical and surgical management and impact of genetic testingElisa Bombardieri, Marianne Rohrbach, Matthias Greutmann, et al.
Nucleic Acids Research|March 31, 2015
New insights into the performance of human whole-exome capture platformsJanine Meienberg, Katja Zerjavic, Irene Keller, et al.
Molecular Genetics and Metabolism|March 14, 2012
Barth syndrome in a female patientLaure Cosson, Annick Toutain, Gilles Simard, et al.
Orphanet Journal of Rare Diseases|October 16, 2020
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvementRoland Stengl, András Bors, Bence Ágg, et al.
Thrombosis and Haemostasis|July 1, 2024
Novel Insights into the Aortic Mechanical Properties of Mice Modeling Hereditary Aortic DiseasesNicolo Dubacher, Kaori Sugiyama, Jeffrey D Smith, et al.
Cardiovascular Research|May 7, 2019
Celiprolol but not losartan improves the biomechanical integrity of the aorta in a mouse model of vascular Ehlers-Danlos syndromeNicolo Dubacher, Justyna Münger, Maria C Gorosabel, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Circulation|March 16, 2013
Acute aortic dissection determines the fate of initially untreated aortic segments in Marfan syndromeFlorian S Schoenhoff, Silvan Jungi, Martin Czerny, et al.
Current Cardiology Reviews|February 18, 2014
Medical treatment of aortic aneurysms in Marfan syndrome and other heritable conditionsChristine H Attenhofer Jost, Matthias Greutmann, Heidi M Connolly, et al.
Circulation|September 2, 2009
Proteomic analysis in aortic media of patients with Marfan syndrome reveals increased activity of calpain 2 in aortic aneurysmsChristiane Pilop, Fabienne Aregger, Robert C Gorman, et al.
Respiratory Research|January 16, 2007
Glutathione S-transferase genotypes modify lung function decline in the general population: SAPALDIA cohort studyMedea Imboden, Sara H Downs, Oliver Senn, et al.
Swiss Medical Weekly|April 4, 2020
Marfan syndrome and related connective tissue disorders in the current era in Switzerland in 103 patients: medical and surgical management and impact of genetic testingElisa Bombardieri, Marianne Rohrbach, Matthias Greutmann, et al.
Nucleic Acids Research|March 31, 2015
New insights into the performance of human whole-exome capture platformsJanine Meienberg, Katja Zerjavic, Irene Keller, et al.
Molecular Genetics and Metabolism|March 14, 2012
Barth syndrome in a female patientLaure Cosson, Annick Toutain, Gilles Simard, et al.
Orphanet Journal of Rare Diseases|October 16, 2020
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvementRoland Stengl, András Bors, Bence Ágg, et al.
Thrombosis and Haemostasis|July 1, 2024
Novel Insights into the Aortic Mechanical Properties of Mice Modeling Hereditary Aortic DiseasesNicolo Dubacher, Kaori Sugiyama, Jeffrey D Smith, et al.
Cardiovascular Research|May 7, 2019
Celiprolol but not losartan improves the biomechanical integrity of the aorta in a mouse model of vascular Ehlers-Danlos syndromeNicolo Dubacher, Justyna Münger, Maria C Gorosabel, et al.
Pageof 3