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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 1 |
2021 | 2 |
2022 | 1 |
2023 | 3 |
2024 | 0 |
Search Results
7 results
Results by year
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Page 1
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.
Orphanet J Rare Dis. 2023 Jan 31;18(1):23. doi: 10.1186/s13023-023-02618-4.
Orphanet J Rare Dis. 2023.
PMID: 36721196
Free PMC article.
Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping.
Sieliwonczyk E, Vandendriessche B, Claes C, Mayeur E, Alaerts M, Holmgren P, Canter Cremers T, Snyders D, Loeys B, Schepers D.
Sieliwonczyk E, et al.
Sci Rep. 2023 Jan 27;13(1):1491. doi: 10.1038/s41598-023-27503-9.
Sci Rep. 2023.
PMID: 36707549
Free PMC article.
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Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes.
Nijak A, Simons E, Vandendriessche B, Van de Sande D, Fransen E, Sieliwończyk E, Van Gucht I, Van Craenenbroeck E, Saenen J, Heidbuchel H, Ponsaerts P, Labro AJ, Snyders D, De Vos W, Schepers D, Alaerts M, Loeys BL.
Nijak A, et al. Among authors: sieliwonczyk e.
Biol Open. 2022 Feb 15;11(2):bio059016. doi: 10.1242/bio.059016. Epub 2022 Feb 23.
Biol Open. 2022.
PMID: 35195246
Free PMC article.
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Inherited Ventricular Arrhythmia in Zebrafish: Genetic Models and Phenotyping Tools.
Sieliwonczyk E, Matchkov VV, Vandendriessche B, Alaerts M, Bakkers J, Loeys B, Schepers D.
Sieliwonczyk E, et al.
Rev Physiol Biochem Pharmacol. 2023;184:33-68. doi: 10.1007/112_2021_65.
Rev Physiol Biochem Pharmacol. 2023.
PMID: 34533615
Review.
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Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death.
Simons E, Labro A, Saenen J, Nijak A, Sieliwonczyk E, Vandendriessche B, Dąbrowska M, Van Craenenbroeck EM, Schepers D, Van Laer L, Loeys BL, Alaerts M.
Simons E, et al. Among authors: sieliwonczyk e.
Eur J Med Genet. 2021 Nov;64(11):104322. doi: 10.1016/j.ejmg.2021.104322. Epub 2021 Aug 23.
Eur J Med Genet. 2021.
PMID: 34438094
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Clinical characterization of the first Belgian SCN5A founder mutation cohort.
Sieliwonczyk E, Alaerts M, Robyns T, Schepers D, Claes C, Corveleyn A, Willems R, Van Craenenbroeck EM, Simons E, Nijak A, Vandendriessche B, Mortier G, Vrints C, Koopman P, Heidbuchel H, Van Laer L, Saenen J, Loeys B.
Sieliwonczyk E, et al.
Europace. 2021 Jun 7;23(6):918-927. doi: 10.1093/europace/euaa305.
Europace. 2021.
PMID: 33221854
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Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report.
Nijak A, Labro AJ, De Wilde H, Dewals W, Peigneur S, Tytgat J, Snyders D, Sieliwonczyk E, Simons E, Van Craenenbroeck E, Schepers D, Van Laer L, Saenen J, Loeys B, Alaerts M.
Nijak A, et al. Among authors: sieliwonczyk e.
Front Cardiovasc Med. 2020 Jul 24;7:117. doi: 10.3389/fcvm.2020.00117. eCollection 2020.
Front Cardiovasc Med. 2020.
PMID: 32850980
Free PMC article.
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