1. Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1. (9th February 2017) Authors: Darin, N.; Hedberg‐Oldfors, C.; Kroksmark, A.‐K.; Moslemi, A.‐R.; Kollberg, G.; Oldfors, A. Journal: European journal of neurology Issue: Volume 24:Number 4(2017:Apr.) Page Start: 587 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cerebrospinal fluid neurofilament light protein as a diagnostic and prognostic biomarker in mitochondrial diseases with CNS involvement. (June 2017) Authors: Sofou, K.; Shahim, P.; Tulinius, M.; Blennow, K.; Zetterberg, H.; Mattsson, N.; Darin, N. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Drug-induced hyperthermia with rhabdomyolysis in CLN3 disease. (July 2022) Authors: Savvidou, A.; Jennions, E.; Wikström, S.; Olsson-Engman, M.; Sofou, K.; Darin, N. Journal: European journal of paediatric neurology Issue: Volume 39(2022) Page Start: 74 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗