A-R Moslemi - JoVE Visualize

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Journal of Neuroimmunology|December 12, 1997

Oligoclonal expansion of muscle infiltrating T cells in inclusion body myositisI M Fyhr, A R Moslemi, A A Mosavi, 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.

Journal of Neuropathology and Experimental Neurology|July 1, 1995

Mitochondrial DNA deletions in muscle fibers in inclusion body myositisA Oldfors, A R Moslemi, I M Fyhr, 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.

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.

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Showing results (21-30 of 27) with videos related to

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You have reached the last page of results.This site can display upto 27 results.

Journal of Neuroimmunology|December 12, 1997

Oligoclonal expansion of muscle infiltrating T cells in inclusion body myositisI M Fyhr, A R Moslemi, A A Mosavi, 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.

Journal of Neuropathology and Experimental Neurology|July 1, 1995

Mitochondrial DNA deletions in muscle fibers in inclusion body myositisA Oldfors, A R Moslemi, I M Fyhr, 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.

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.

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