Genes in thoracic aortic aneurysms/dissections - do they matter?

Por De Backer, Julie, Campens, Laurence, De Paepe, Anne
Publicado em 2013

Type B aortic dissection triggered by heart transplantation in a patient with Marfan syndrome

Por Audenaert, Tjorven, De Pauw, Michel, François, Katrien, De Backer, Julie
Publicado no BMJ Case Rep (2015)

FBN1: The Disease-Causing Gene for Marfan Syndrome and Other Genetic Disorders

Por Sakai, Lynn Y., Keene, Douglas R., Renard, Marjolijn, De Backer, Julie
Publicado no Gene (2016)

Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review

Por Demolder, Anthony, von Kodolitsch, Yskert, Muiño-Mosquera, Laura, De Backer, Julie
Publicado no Diagnostics (Basel) (2020)

Genes in Thoracic Aortic Aneurysms and Dissections – Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice

Por De Backer, Julie, Renard, Marjolijn, Campens, Laurence, François, Katrien, Callewaert, Bert, Coucke, Paul, De Paepe, Anne
Publicado no Aorta (Stamford) (2013)

Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients

Por Campens, Laurence, Callewaert, Bert, Muiño Mosquera, Laura, Renard, Marjolijn, Symoens, Sofie, De Paepe, Anne, Coucke, Paul, De Backer, Julie
Publicado no Orphanet J Rare Dis (2015)

Propagation-based phase-contrast synchrotron imaging of aortic dissection in mice: from individual elastic lamella to 3D analysis

Por Logghe, Gerlinde, Trachet, Bram, Aslanidou, Lydia, Villaneuva-Perez, Pablo, De Backer, Julie, Stergiopulos, Nikolaos, Stampanoni, Marco, Aoki, Hiroki, Segers, Patrick
Publicado no Sci Rep (2018)

Sex, pregnancy and aortic disease in Marfan syndrome

Por Renard, Marjolijn, Muiño-Mosquera, Laura, Manalo, Elise C., Tufa, Sara, Carlson, Eric J., Keene, Douglas R., De Backer, Julie, Sakai, Lynn Y.
Publicado no PLoS One (2017)

MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking Water

Por Steijns, Felke, Bracke, Nathalie, Renard, Marjolijn, De Backer, Julie, Sips, Patrick, Debunne, Nathan, Wynendaele, Evelien, Verbeke, Frederick, De Spiegeleer, Bart, Campens, Laurence
Publicado no Front Pharmacol (2020)

Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome

Por Muiño‐Mosquera, Laura, Bauters, Fré, Dhondt, Karlien, De Wilde, Hans, Jordaens, Luc, De Groote, Katya, De Wolf, Daniel, Hertegonne, Katrien, De Backer, Julie
Publicado no Mol Genet Genomic Med (2019)

Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious Mice

Por Steijns, Felke, Tóth, Máté I., Demolder, Anthony, Larsen, Lars E., Desloovere, Jana, Renard, Marjolijn, Raedt, Robrecht, Segers, Patrick, De Backer, Julie, Sips, Patrick
Publicado no Sensors (Basel) (2020)

Effects of fibrillin mutations on the behavior of heart muscle cells in Marfan syndrome

Por Aalders, Jeffrey, Léger, Laurens, Van der Meeren, Louis, Van den Vreken, Natasja, Skirtach, Andre G., Sinha, Sanjay, De Backer, Julie, van Hengel, Jolanda
Publicado no Sci Rep (2020)

Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome

Por Steijns, Felke, Renard, Marjolijn, Vanhomwegen, Marine, Vermassen, Petra, Desloovere, Jana, Raedt, Robrecht, Larsen, Lars E., Tóth, Máté I., De Backer, Julie, Sips, Patrick
Publicado no Int J Mol Sci (2020)

Myocardial disease and ventricular arrhythmia in Marfan syndrome: a prospective study

Por Muiño-Mosquera, Laura, De Wilde, Hans, Devos, Daniel, Babin, Danilo, Jordaens, Luc, Demolder, Anthony, De Groote, Katya, De Wolf, Daniel, De Backer, Julie
Publicado no Orphanet J Rare Dis (2020)

A Genotype-First Approach to Exploring Mendelian Cardiovascular Traits with Clear External Manifestations

Por Wenger, Brittany M., Patel, Nihir, Lui, Madeline, Moscati, Arden, Do, Ron, Stewart, Douglas R., Tartaglia, Marco, Muiño-Mosquera, Laura, De Backer, Julie, Kontorovich, Amy R., Gelb, Bruce D.
Publicado no Genet Med (2020)

Aneurysm-osteoarthritis syndrome with visceral and iliac artery aneurysms

Por van der Linde, Denise, Verhagen, Hence J. M., Moelker, Adriaan, van de Laar, Ingrid M. B. H., Van Herzeele, Isabelle, De Backer, Julie, Dietz, Harry C., Roos-Hesselink, Jolien W.
Publicado em 2012

Hungarian Marfan family with large FBN1 deletion calls attention to copy number variation detection in the current NGS era

Por Benke, Kálmán, Ágg, Bence, Meienberg, Janine, Kopps, Anna M., Fattorini, Nathalie, Stengl, Roland, Daradics, Noémi, Pólos, Miklós, Bors, András, Radovits, Tamás, Merkely, Béla, De Backer, Julie, Szabolcs, Zoltán, Mátyás, Gábor
Publicado no J Thorac Dis (2018)

Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome

Por von Kodolitsch, Yskert, De Backer, Julie, Schüler, Helke, Bannas, Peter, Behzadi, Cyrus, Bernhardt, Alexander M, Hillebrand, Mathias, Fuisting, Bettina, Sheikhzadeh, Sara, Rybczynski, Meike, Kölbel, Tilo, Püschel, Klaus, Blankenberg, Stefan, Robinson, Peter N
Publicado no Appl Clin Genet (2015)

Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse()

Por Rippe, Moritz, De Backer, Julie, Kutsche, Kerstin, Mosquera, Laura Muiño, Schüler, Helke, Rybczynski, Meike, Bernhardt, Alexander M., Keyser, Britta, Hillebrand, Mathias, Mir, Thomas S., Berger, Jürgen, Blankenberg, Stefan, Koschyk, Dietmar, von Kodolitsch, Yskert
Publicado no Int J Cardiol Heart Vasc (2016)

SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections

Por Duan, Xue-Yan, Guo, Dong-chuan, Regalado, Ellen S., Shen, Hong, Coselli, Joseph S., Estrera, Anthony L., Safi, Hazim J., Bamshad, Michael J., Nickerson, Deborah A., LeMaire, Scott A., De Backer, Julie, Milewicz, Dianna M.
Publicado no Eur J Hum Genet (2019)