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Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1993
Fatal neonatal lactic acidosis with respiratory insufficiency due to complex I and IV deficiencyU von Döbeln, R Wibom, H Ahlman, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 5, 2002
Chronic cobalt exposure affects antioxidants and ATP production in rat myocardiumN Clyne, C Hofman-Bang, Y Haga, et al.
Journal of the Neurological Sciences|December 1, 1996
Muscle morphology and mitochondrial investigations of a family with autosomal dominant cerebellar ataxia and retinal degeneration mapped to chromosome 3p12-p21.1L Forsgren, R Libelius, M Holmberg, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|April 1, 1990
The effect of cobalt on mitochondrial ATP-production in the rat myocardium and skeletal muscleN Clyne, R Wibom, N Havu, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|October 1, 1990
The intracellular distribution of cobalt in exposed and unexposed rat myocardiumN Clyne, B Persson, N Havu, et al.
Endocrinology|June 2, 1998
Glucose metabolism in Goto-Kakizaki rat isletsZ C Ling, S Efendic, R Wibom, et al.
Acta Neurologica Scandinavica|October 1, 1996
Monozygotic twins with MELAS-like syndrome lacking ragged red fibers and lactacidaemiaA Melberg, P Akerlund, R Raininko, et al.
Journal of the Neurological Sciences|December 1, 1995
Autosomal dominant cerebellar ataxia deafness and narcolepsyA Melberg, J Hetta, N Dahl, et al.
The Journal of Clinical Investigation|October 1, 1991
Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defectR G Haller, K G Henriksson, L Jorfeldt, et al.
Science Advances|April 6, 2019
Modulation of mtDNA copy number ameliorates the pathological consequences of a heteroplasmic mtDNA mutation in the mouseR Filograna, C Koolmeister, M Upadhyay, et al.
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