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Acta Neuropathologica|July 27, 2000
Multiple mitochondrial DNA deletions in hereditary inclusion body myopathyM Jansson, N Darin, M Kyllerman, et al.
Metabolism: Clinical and Experimental|August 1, 1992
Cortisol secretion in relation to body fat distribution in obese premenopausal womenP Mårin, N Darin, T Amemiya, et al.
Neurology|October 15, 2003
SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiencyA-R Moslemi, M Tulinius, N Darin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 18, 2022
Drug-induced hyperthermia with rhabdomyolysis in CLN3 diseaseA Savvidou, E Jennions, S Wikström, et al.
Lakartidningen|February 1, 1995
[Gene amplification in viral CNS infections. Rapid diagnostic identification of herpesviruses]T Bergström, S Olofsson, M Studahl, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa geneT Martinsson, A Oldfors, N Darin, et al.
Neuropediatrics|May 28, 2008
Progressive encephalopathy and complex I deficiency associated with mutations in MTND1A-R Moslemi, N Darin, M Tulinius, et al.
Neuropediatrics|December 19, 2003
Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiencyN Darin, A-R Moslemi, S Lebon, et al.
European Journal of Neurology|February 10, 2017
Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1N Darin, C Hedberg-Oldfors, A-K Kroksmark, et al.
Neurology|March 13, 2002
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with ageH Tajsharghi, L-E Thornell, N Darin, et al.
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