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Mitochondrion|March 23, 2007
Molecular genetic and clinical aspects of mitochondrial disorders in childhoodAli-Reza Moslemi, Niklas DarinPlos One|September 17, 2013
Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue culturesSaba Abdul-Hussein, Karin Rahl, Ali-Reza Moslemi, et al.Neuromuscular Disorders : NMD|November 22, 2011
Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutationCarola Hedberg, Christopher Lindberg, Gyöngyvér Máthé, et al.Journal of Neuropathology and Experimental Neurology|March 9, 2005
Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit IGittan Kollberg, Ali-Reza Moslemi, Christopher Lindberg, et al.Neuromuscular Disorders : NMD|May 24, 2005
Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletionMár Tulinius, Ali-Reza Moslemi, Niklas Darin, et al.European Journal of Medical Genetics|November 19, 2008
A patient with two mitochondrial DNA mutations causing PEO and LHONAtle Melberg, Ali-Reza Moslemi, Oscar Palm, et al.The New England Journal of Medicine|April 2, 2010
Glycogenin-1 deficiency and inactivated priming of glycogen synthesisAli-Reza Moslemi, Christopher Lindberg, Johanna Nilsson, et al.Brain : a Journal of Neurology|April 29, 2005
Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNAMikko Kärppä, Riitta Herva, Ali-Reza Moslemi, et al.BMC Genetics|June 2, 2016
Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndromeAriana Kariminejad, Navid Almadani, Atefeh Khoshaeen, et al.Neuromuscular Disorders : NMD|February 2, 2015
Mitochondrial pathology in inclusion body myositisUlrika Lindgren, Sara Roos, Carola Hedberg Oldfors, et al.Pageof 4