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Neuromuscular Disorders : NMD|June 24, 2014
Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutationsS Roos, U Lindgren, C Ehrstedt, 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.
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.
Clinical and Experimental Rheumatology|June 16, 2001
Estrogen receptor alpha in giant cell arteritis: a molecular genetic studyV Petursdottir, A R Moslemi, M Persson, et al.
Scandinavian Journal of Immunology|January 1, 1996
Limited T-cell receptor V gene usage in inclusion body myositisI M Fyhr, A R Moslemi, A Tarkowski, et al.
Neuromuscular Disorders : NMD|December 9, 2003
A novel mutation in the mitochondrial tRNA(Phe) gene associated with mitochondrial myopathyA-R Moslemi, C Lindberg, J Toft, et al.
Neurology|January 25, 2006
Mitochondrial abnormalities in inclusion-body myositisA Oldfors, A R Moslemi, L Jonasson, 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.
Neuropediatrics|May 28, 2008
Progressive encephalopathy and complex I deficiency associated with mutations in MTND1A-R Moslemi, N Darin, M Tulinius, 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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