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Journal of Musculoskeletal & Neuronal Interactions|March 1, 2013
Whole body vibration therapy in patients with Duchenne muscular dystrophy--a prospective observational studyA-C Söderpalm, A-K Kroksmark, P Magnusson, 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.
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.
Pediatric Research|December 1, 1992
Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduriaE Holme, J Greter, C E Jacobson, 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.
Human Genetics|March 10, 1999
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiencyA B Van Kuilenburg, P Vreken, N G Abeling, et al.
Scientific Reports|December 22, 2017
Evaluation of serum MMP-9 as predictive biomarker for antisense therapy in DuchenneA Lourbakos, N Yau, P de Bruijn, et al.
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