Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population
Sieliwonczyk, Ewa, Alaerts, Maaike, Simons, Eline, Snyders, Dirk, Nijak, Aleksandra, Vandendriessche, Bert, Schepers, Dorien, Akdeniz, Dogan, Van Craenenbroeck, Emeline, Knaepen, Katleen, Rabaut, Laura, Heidbuchel, Hein, Van Laer, Lut, Saenen, Johan, Labro, Alain J, Loeys, Bart
Published in Orphanet journal of rare diseases (31.01.2023)
Published in Orphanet journal of rare diseases (31.01.2023)
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Journal Article
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes
Nijak, Aleksandra, Simons, Eline, Vandendriessche, Bert, Van de Sande, Dieter, Fransen, Erik, Sieliwończyk, Ewa, Van Gucht, Ilse, Van Craenenbroeck, Emeline, Saenen, Johan, Heidbuchel, Hein, Ponsaerts, Peter, Labro, Alain J, Snyders, Dirk, De Vos, Winnok, Schepers, Dorien, Alaerts, Maaike, Loeys, Bart L
Published in Biology open (15.02.2022)
Published in Biology open (15.02.2022)
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Journal Article
Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin
Boen, Hanne M., Vandendriessche, Bert, Schippers, Jolien, Rabaut, Laura, Nijak-Paeske, Aleksandra, Ponsaerts, Peter, Van Craenenbroeck, Emeline M., Loeys, Bart, Alaerts, Maaike
Published in Stem cell research (01.12.2024)
Published in Stem cell research (01.12.2024)
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Journal Article
Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report
Nijak, Aleksandra, Labro, Alain J., De Wilde, Hans, Dewals, Wendy, Peigneur, Steve, Tytgat, Jan, Snyders, Dirk, Sieliwonczyk, Ewa, Simons, Eline, Van Craenenbroeck, Emeline, Schepers, Dorien, Van Laer, Lut, Saenen, Johan, Loeys, Bart, Alaerts, Maaike
Published in Frontiers in cardiovascular medicine (24.07.2020)
Published in Frontiers in cardiovascular medicine (24.07.2020)
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Journal Article
Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen–glucose Deprivation
Van Breedam, Elise, Nijak, Aleksandra, Buyle-Huybrecht, Tamariche, Di Stefano, Julia, Boeren, Marlies, Govaerts, Jonas, Quarta, Alessandra, Swartenbroekx, Tine, Jacobs, Eva Z., Menten, Björn, Gijsbers, Rik, Delputte, Peter, Alaerts, Maaike, Hassannia, Behrouz, Loeys, Bart, Berneman, Zwi, Timmermans, Jean-Pierre, Jorens, Philippe G., Vanden Berghe, Tom, Fransen, Erik, Wouters, An, De Vos, Winnok H., Ponsaerts, Peter
Published in Neurotherapeutics (01.03.2022)
Published in Neurotherapeutics (01.03.2022)
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Journal Article
Correction to: Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen–glucose Deprivation
Van Breedam, Elise, Nijak, Aleksandra, Buyle-Huybrecht, Tamariche, Di Stefano, Julia, Boeren, Marlies, Govaerts, Jonas, Quarta, Alessandra, Swartenbroekx, Tine, Z. Jacobs, Eva, Menten, Björn, Gijsbers, Rik, Delputte, Peter, Alaerts, Maaike, Hassannia, Behrouz, Loeys, Bart, Berneman, Zwi, Timmermans, Jean-Pierre, G. Jorens, Philippe, Vanden Berghe, Tom, Fransen, Erik, Wouters, An, H. De Vos, Winnok, Ponsaerts, Peter
Published in Neurotherapeutics (01.07.2022)
Published in Neurotherapeutics (01.07.2022)
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Journal Article
Clinical characterization of the first Belgian SCN5A founder mutation cohort
Sieliwonczyk, Ewa, Alaerts, Maaike, Robyns, Tomas, Schepers, Dorien, Claes, Charlotte, Corveleyn, Anniek, Willems, Rik, Van Craenenbroeck, Emeline M, Simons, Eline, Nijak, Aleksandra, Vandendriessche, Bert, Mortier, Geert, Vrints, Christiaan, Koopman, Pieter, Heidbuchel, Hein, Van Laer, Lut, Saenen, Johan, Loeys, Bart
Published in Europace (London, England) (07.06.2021)
Published in Europace (London, England) (07.06.2021)
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Journal Article
Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death
Simons, Eline, Labro, Alain, Saenen, Johan, Nijak, Aleksandra, Sieliwonczyk, Ewa, Vandendriessche, Bert, Dąbrowska, Małgorzata, Van Craenenbroeck, Emeline M., Schepers, Dorien, Van Laer, Lut, Loeys, Bart L., Alaerts, Maaike
Published in European journal of medical genetics (01.11.2021)
Published in European journal of medical genetics (01.11.2021)
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Journal Article
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation
Nijak, Aleksandra, Alaerts, Maaike, Kuiperi, Cuno, Corveleyn, Anniek, Suys, Bert, Paelinck, Bernard, Saenen, Johan, Van Craenenbroeck, Emeline, Van Laer, Lut, Loeys, Bart, Verstraeten, Aline
Published in European journal of medical genetics (01.01.2018)
Published in European journal of medical genetics (01.01.2018)
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Journal Article
Epigenetics: the guardian of pluripotency and differentiation
GŁADYCH, Marta, NIJAK, Aleksandra, LOTA, Paula, OLEKSIEWICZ, Urszula
Published in Turkish journal of biology (2016)
Published in Turkish journal of biology (2016)
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Journal Article
Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report
Nijak, Aleksandra, Labro, Alain J, De Wilde, Hans, Dewals, Wendy, Peigneur, Steve, Tytgat, Jan, Snyders, Dirk, Sieliwonczyk, Ewa, Simons, Eline, Van Craenenbroeck, Emeline, Schepers, Dorien, Van Laer, Lut, Saenen, Johan, Loeys, Bart, Alaerts, Maaike
Published in Frontiers in cardiovascular medicine (01.01.2020)
Published in Frontiers in cardiovascular medicine (01.01.2020)
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