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Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.
Majamaa K, Moilanen JS, Uimonen S, Remes AM, Salmela PI, Kärppä M, Majamaa-Voltti KA, Rusanen H, Sorri M, Peuhkurinen KJ, Hassinen IE. Majamaa K, et al. Among authors: moilanen js. Am J Hum Genet. 1998 Aug;63(2):447-54. doi: 10.1086/301959. Am J Hum Genet. 1998. PMID: 9683591 Free PMC article.
Familial aggregation of Parkinson's disease in a Finnish population.
Autere JM, Moilanen JS, Myllylä VV, Majamaa K. Autere JM, et al. Among authors: moilanen js. J Neurol Neurosurg Psychiatry. 2000 Jul;69(1):107-9. doi: 10.1136/jnnp.69.1.107. J Neurol Neurosurg Psychiatry. 2000. PMID: 10864614 Free PMC article.
Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome.
Remes AM, Kärppä M, Moilanen JS, Rusanen H, Hassinen IE, Majamaa K, Uimonen S, Sorri M, Salmela PI, Karvonen SL, Karvonen SL. Remes AM, et al. Among authors: moilanen js. J Neurol Neurosurg Psychiatry. 2003 Aug;74(8):1158-9. doi: 10.1136/jnnp.74.8.1158. J Neurol Neurosurg Psychiatry. 2003. PMID: 12876264 Free PMC article. No abstract available.
80 results