Ghent University Academic Bibliography

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iPSC-cardiomyocyte models of Brugada syndrome : achievements, challenges and future perspectives

Aleksandra Nijak, Johan Saenen, Alain J Labro (UGent) , Dorien Schepers, Bart L. Loeys and Maaike Alaerts

(2021) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 22(6).
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Compound heterozygous SCN5A mutations in severe sodium channelopathy with Brugada syndrome : a case report

Aleksandra Nijak, Alain J Labro (UGent) , Hans De Wilde (UGent) , Wendy Dewals, Steve Peigneur, Jan Tytgat, Dirk Snyders, Ewa Sieliwonczyk, Eline Simons, Emeline Van Craenenbroeck, et al.

(2020) FRONTIERS IN CARDIOVASCULAR MEDICINE. 7.
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Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia

Nikhita Ajit Bolar, Christelle Golzio, Martina Živná, Gaëlle Hayot, CHRISTINE VAN HEMELRIJK (UGent) , Dorien Schepers, Geert Vandeweyer, Alexander Hoischen, Jeroen R Huyghe, Ann Raes (UGent) , et al.

(2016) AMERICAN JOURNAL OF HUMAN GENETICS. 99(1). p.174-187
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Lessons learned from the intersection of two frequent monogenic disorders : the Marfan syndrome and autosomal dominant polycystic kidney disease

Dorien Schepers, Stéphanie Dautricourt, Lauranne De Decker, Ann Raes (UGent) , Lut Van Laer and Bart Loeys (UGent)

(2013) PROCEEDINGS OF THE BELGIAN ROYAL ACADEMIES OF MEDICINE. 2. p.179-197

Academic Bibliography

iPSC-cardiomyocyte models of Brugada syndrome : achievements, challenges and future perspectives

Compound heterozygous SCN5A mutations in severe sodium channelopathy with Brugada syndrome : a case report

Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia

Lessons learned from the intersection of two frequent monogenic disorders : the Marfan syndrome and autosomal dominant polycystic kidney disease

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