Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3Nahid Khan, Anu Suomalainen, Mari Auranen et al.|EMBO Molecular Medicine|2014Cited by 386
Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA DeletionsSaara Forsström, Anu Suomalainen, Christopher B. Jackson et al.|Cell Metabolism|2019Cited by 262
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiencySarah J. Brockmann, Jochen H. Weishaupt, Axel Freischmidt et al.|Human Molecular Genetics|2017Cited by 38
Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1CMari Auranen, Emil Ylikallio, Jussi Toppila et al.|Molecular Case Studies|2017Cited by 34
Screening for late-onset Pompe disease in FinlandJohanna Palmio, Bjarne Udd, Mari Auranen et al.|Neuromuscular Disorders|2014Cited by 29