1. Genetic aetiology of ophthalmological manifestations in children – a focus on mitochondrial disease‐related symptoms. (8th October 2015) Authors: Widgren, Paula; Hurme, Anri; Falck, Aura; Keski‐Filppula, Riikka; Remes, Anne M; Moilanen, Jukka; Majamaa, Kari; Kervinen, Marko; Uusimaa, Johanna Journal: Acta ophthalmologica Issue: Volume 94:Number 1(2016) Page Start: 83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Leber hereditary optic neuropathy mutations and toxic‐genetic optic neuropathy — Authors' response. (25th February 2013) Authors: Kervinen, Marko; Widgren, Paula; Saarela, Ville; Uusimaa, Johanna; Remes, Anne Journal: Acta ophthalmologica Issue: Volume 92:Number 1(2014) Page Start: e78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco‐alcohol amblyopia. (12th September 2012) Authors: Korkiamäki, Paula; Kervinen, Marko; Karjalainen, Karoliina; Majamaa, Kari; Uusimaa, Johanna; Remes, Anne M. Journal: Acta ophthalmologica Issue: Volume 91:Number 7(2013) Page Start: 630 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗