Seija Uimonen

Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

Kari Majamaa, Jukka S. Moilanen, Seija Uimonen et al. · The American Journal of Human Genetics · 1998 · 383 citations · Full text

Strokelike Episodes, Lactic Acidosis, Mendelian Disorder +11

A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA

Kirsi Majamaa‐Voltti, Satu Winqvist, Anne M. Remes et al. · Neurology · 2006 · 67 citations

Hearing impairment in patients with 3243A→G mtDNA mutation: phenotype and rate of progression

Seija Uimonen, Jukka S. Moilanen, Martti Sorri et al. · Human Genetics · 2001 · 60 citations

Mendelian Disorder, Genetic Disorder, Genetics +11

Do We Know the Real Need for Hearing Rehabilitation at the Population Level? Hearing Impairments in the 5- to 75-Year-Old Cross-Sectional Finnish Population

Seija Uimonen, Kerttu Huttunen, Katariina Jounio‐Ervasti et al. · British Journal of Audiology · 1999 · 55 citations

Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population

Anne M. Remes, Kirsi Majamaa‐Voltti, Mikko Kärppä et al. · Neurology · 2005 · 51 citations

Genetic Testing, Genetics, Genetic Epidemiology +17