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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.
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.
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.
Neurology|December 3, 2008
New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutationsM Ohlsson, S Quijano-Roy, N Darin, 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.
Genes and Immunity|March 24, 2017
The immunogenetics of narcolepsy associated with A(H1N1)pdm09 vaccination (Pandemrix) supports a potent gene-environment interactionI L Bomfim, F Lamb, K Fink, et al.
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