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Neuropediatrics|May 28, 2008
Progressive encephalopathy and complex I deficiency associated with mutations in MTND1A-R Moslemi, N Darin, M Tulinius, et al.
Neuropediatrics|May 31, 2003
Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp geneM Tulinius, A-R Moslemi, N Darin, et al.
Annals of Neurology|March 23, 2001
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalitiesN Darin, A Oldfors, A R Moslemi, et al.
Neuropediatrics|October 12, 2005
Two new mutations in the MTATP6 gene associated with Leigh syndromeA-R Moslemi, N Darin, M Tulinius, 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.
Neuromuscular Disorders : NMD|July 23, 1998
Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibresA R Moslemi, M Tulinius, E Holme, 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.
Neuromuscular Disorders : NMD|June 30, 2006
Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) geneN Darin, G Kollberg, A-R Moslemi, et al.
The British Journal of Ophthalmology|April 14, 2010
Ophthalmological findings in children and young adults with genetically verified mitochondrial diseaseM A Grönlund, A K Seyedi Honarvar, S Andersson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 21, 2007
Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2IN Darin, A-K Kroksmark, A-C Ahlander, et al.
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