1. Characterization of CoQ10 biosynthesis in fibroblasts of patients with primary and secondary CoQ10 deficiency. Issue 1 (18th June 2013) Authors: Buján, Nuria; Arias, Angela; Montero, Raquel; García‐Villoria, Judit; Lissens, Willy; Seneca, Sara; Espinós, Carmen; Navas, Plácido; De Meirleir, Linda; Artuch, Rafael; Briones, Paz; Ribes, Antonia Journal: Journal of inherited metabolic disease Issue: Volume 37:Issue 1(2014) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical implementation of gene panel testing for lysosomal storage diseases. Issue 2 (11th December 2018) Authors: Gheldof, Alexander; Seneca, Sara; Stouffs, Katrien; Lissens, Willy; Jansen, Anna; Laeremans, Hilde; Verloo, Patrick; Schoonjans, An‐Sofie; Meuwissen, Marije; Barca, Diana; Martens, Geert; De Meirleir, Linda Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 2(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Effect of Resveratrol on Cultured Skin Fibroblasts from Patients with Oxidative Phosphorylation Defects. (26th April 2013) Authors: De Paepe, Boel; Vandemeulebroecke, Katrien; Smet, Joél; Vanlander, Arnaud; Seneca, Sara; Lissens, Willy; Van Hove, Johan LK; Deschepper, Ellen; Briones, Paz; Van Coster, Rudy Journal: Phytotherapy research Issue: Volume 28:Number 2(2014:Feb.) Page Start: 312 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells. Issue 16 (27th June 2018) Authors: Dastidar, Sumitava; Ardui, Simon; Singh, Kshitiz; Majumdar, Debanjana; Nair, Nisha; Fu, Yanfang; Reyon, Deepak; Samara, Ermira; Gerli, Mattia F M; Klein, Arnaud F; De Schrijver, Wito; Tipanee, Jaitip; Seneca, Sara; Tulalamba, Warut; Wang, Hui; Chai, Yoke Chin; In't Veld, Peter... Journal: Nucleic acids research Issue: Volume 46:Issue 16(2018) Page Start: 8275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the MT-ND6 gene. (4th July 2021) Authors: Vandeputte, Justine; Van Heetvelde, Mattias; Van Cauwenbergh, Caroline; Seneca, Sara; De Baere, Elfride; Leroy, Bart P; De Zaeytijd, Julie Journal: Ophthalmic genetics Issue: Volume 42:Number 4(2021) Page Start: 440 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mutation of the iron‐sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy. Issue 6 (14th May 2015) Authors: Debray, François‐Guillaume; Stümpfig, Claudia; Vanlander, Arnaud V.; Dideberg, Vinciane; Josse, Claire; Caberg, Jean‐Hubert; Boemer, François; Bours, Vincent; Stevens, René; Seneca, Sara; Smet, Joél; Lill, Roland; van Coster, Rudy Journal: Journal of inherited metabolic disease Issue: Volume 38:Issue 6(2015) Page Start: 1147 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Near-Infrared Spectroscopy Screening to Allow Detection of Pathogenic Mitochondrial DNA Variants in Individuals with Unexplained Abnormal Fatigue: A Preliminary Study. Issue 5 (May 2018) Authors: Celie, Bert M.; Mariman, An; Boone, Jan; Delesie, Liesbeth; Tobback, Els; Seneca, Sara; De Paepe, Boel; Vogelaers, Dirk; Van Coster, Rudy N.; Bourgois, Jan G. Journal: Applied spectroscopy Issue: Volume 72:Issue 5(2018) Page Start: 715 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 gene. (February 2016) Authors: de Filette, Jeroen; Hasaerts, Danielle; Seneca, Sara; Gheldof, Alexander; Stouffs, Katrien; Keymolen, Kathelijn; Velkeniers, Brigitte Journal: Neurology Issue: Volume 2:Number 1(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Sertoli Cell-Only Syndrome: Behind the Genetic Scenes. (26th January 2016) Authors: Stouffs, Katrien; Gheldof, Alexander; Tournaye, Herman; Vandermaelen, Deborah; Bonduelle, Maryse; Lissens, Willy; Seneca, Sara Other Names: Suneeta Mittal Academic Editor. Journal: BioMed research international Issue: Volume 2016(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Severe biventricular hypertrophy in MELAS mitochondrial disease. (1st September 2016) Authors: Rosseel, Liesbeth; Breckpot, Jeroen; Debrauwere, Jan; Seneca, Sara; Buysschaert, Ian Journal: European heart journal Issue: Volume 18:Number 1(2017:Jan.) Page Start: 112 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗