Anna H. Hakonen

FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study

Anu Suomalainen, Jenni M. Elo, Kirsi H. Pietiläinen et al. · The Lancet Neurology · 2011 · 414 citations · Full text

Diagnostic Study, Fibrosis, Mitochondrial Function +3

Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin

Anna H. Hakonen, Silja Heiskanen, Vesa Juvonen et al. · The American Journal of Human Genetics · 2005 · 305 citations · Full text

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +10

Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion

Anna H. Hakonen, Pirjo Isohanni, Anders Paetau et al. · Brain · 2007 · 197 citations · Full text

Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease

Petri Luoma, Johanna Eerola, Sofia Ahola et al. · Neurology · 2007 · 154 citations

Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion

Anna H. Hakonen, Steffi Goffart, Sanna Marjavaara et al. · Human Molecular Genetics · 2008 · 135 citations · Full text

Mitochondrial Dysfunction, Neurological Disorder, Genetics +22