Laurence A. Bindoff
Haukeland University Hospital(NO)University of Bergen(NO)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, Genetic Neurodegenerative Diseases, ATP Synthase and ATPases Research, Muscle Physiology and Disorders
Most-Cited Works
- → Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease(2001)539 cited
- → Correlation between Genetic and Geographic Structure in Europe(2008)515 cited
- → Multi-system neurological disease is common in patients with OPA1 mutations(2010)439 cited
- → FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study(2011)419 cited
- Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.(1991)
- → The epidemiology of pathogenic mitochondrial DNA mutations(2000)394 cited
- → Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin