| Broad phenotypic variability in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1 K Björkman, K Sofou, N Darin, E Holme, G Kollberg, J Asin-Cayuela, ... Mitochondrion 21, 33-40, 2015 | 37 | 2015 |
| Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study K Björkman, J Vissing, E Østergaard, LA Bindoff, IFM de Coo, M Engvall, ... Journal of Medical Genetics 60 (1), 65-73, 2023 | 9 | 2023 |
| Genotype-phenotype correlations in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1 K Björkman, K Sofou, N Darin, E Holme, G Kollberg, J Asin-Cayuela, ... Euromit 2014, 15-19 juni, Tampere, Finland, 2014 | | 2014 |
| PP6. 6–1797 Isolated complex I deficiency and atypical clinical courses in three patients due to novel mutations in NDUFS1 and NDUFV1 K Björkman, K Sofou, N Darin, G Kollberg, E Holme, M Tulinius, A Oldfors, ... European Journal of Paediatric Neurology, S46, 2013 | | 2013 |
| Traditional medicine in Rwanda K Björkman, E Carlsson, J Falkenström, A Levin | | |
| Personal and professional development effects of involving interns as responsible for improvement processes K Björkman, E Almquist, U Strandman, P Andréll, C Finizia | | |
