Aleksandra Nijak
Antwerpen, VLG, Belgium
Last Updated: 09/26/2026
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Found 11 publications
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.
Journal: Orphanet journal of rare diseases
Published: July 19, 2022
Correction to: Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen-glucose Deprivation.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: June 21, 2022
Correction to: Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen-glucose Deprivation.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: June 21, 2022
Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen-glucose Deprivation.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: February 14, 2022
Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutation.
Journal: Stem cell research
Published: February 09, 2022
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes.
Journal: Biology open
Published: September 02, 2021
Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death.
Journal: European journal of medical genetics
Published: February 15, 2021
iPSC-Cardiomyocyte Models of Brugada Syndrome-Achievements, Challenges and Future Perspectives.
Journal: International journal of molecular sciences
Published: January 17, 2021
Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report.
Journal: Frontiers in cardiovascular medicine
Published: April 03, 2020
Clinical characterization of the first Belgian SCN5A founder mutation cohort.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: March 20, 2020
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation.
Journal: European journal of medical genetics
Published: July 19, 2017
Showing 1-11 of 11
Last Updated: 09/26/2026