Ghent University Academic Bibliography

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International registry of patients carrying TGFBR1 or TGFBR2 mutations results of the MAC (Montalcino Aortic Consortium)

Guillaume Jondeau, Jacques Ropers, Ellen Regalado, Alan Braverman, Arturo Evangelista, Guisela Teixedo, Julie De Backer (UGent) , Laura Muiño Mosquera (UGent) , Sophie Naudion, Cecile Zordan, et al.

(2016) CIRCULATION-CARDIOVASCULAR GENETICS. 9(6). p.548-558
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Intercalated discs and arrhythmogenic cardiomyopathy

Alessandra Rampazzo, Martina Calore, Jolanda van Hengel (UGent) and Frans Van Roy (UGent)

(2014) CIRCULATION-CARDIOVASCULAR GENETICS. 7(6). p.930-940
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Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

Gary F Mitchell, Germaine C Verwoert, Kirill V Tarasov, Aaron Isaacs, Albert V Smith, . Yasmin, Ernst Rietzschel (UGent) , Toshiko Tanaka, Yongmei Liu, Afshin Parsa, et al.

(2012) CIRCULATION-CARDIOVASCULAR GENETICS. 5(1). p.81-90
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Enabling computational proteomics by public and local data management systems

Kenny Helsens (UGent) and Lennart Martens (UGent)

(2012) CIRCULATION-CARDIOVASCULAR GENETICS. 5(2). p.O9-O15
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- Journal Article
- A1
A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death

Roos F Marsman, Abdenasser Bardai, Alex V Postma, Jan CJ Res, Tamara T Koopmann, Leander Beekman, Allard C van der Wal, Yigal M Pinto, Ronald H Lekanne Deprez, Arthur AM Wilde, et al.

(2011) CIRCULATION-CARDIOVASCULAR GENETICS. 4(3). p.280-287
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Chylomicronemia with low Postheparin Lipoprotein Lipase levels in the setting of GPIHBP1 defects

Remco Franssen, Stephen G Young, Frank Peelman (UGent) , Jozef Hertecant, Jeroen A Sierts, Alida WM Schimmel, Andre Bensadoun, John JP Kastelein, Loren G Fong, Geesje M Dallinga-Thie, et al.

(2010) CIRCULATION-CARDIOVASCULAR GENETICS. 3(2). p.169-178

Academic Bibliography

International registry of patients carrying TGFBR1 or TGFBR2 mutations results of the MAC (Montalcino Aortic Consortium)

Intercalated discs and arrhythmogenic cardiomyopathy

Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

Enabling computational proteomics by public and local data management systems

A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death

Chylomicronemia with low Postheparin Lipoprotein Lipase levels in the setting of GPIHBP1 defects

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