Anne Kjersti Erichsen

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

Giovanni Stévanin, Hamid Azzedine, Paola S. Denora et al. · Brain · 2007 · 246 citations

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study

Anne Kjersti Erichsen, Jeanette Koht, Asbjørg Stray‐Pedersen et al. · Brain · 2009 · 207 citations

Family Medicine, Rare Diseases, Mendelian Disorder +15

STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity

Ketil Heimdal, Mònica Sánchez-Guixé, Ingvild Aukrust et al. · Orphanet Journal of Rare Diseases · 2014 · 70 citations · Full text

Hereditary Spastic Paraplegia 3A Associated With Axonal Neuropathy

Neviana Ivanova, Kristl G. Claeys, Tine Deconinck et al. · Archives of Neurology · 2007 · 51 citations

Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia

Anne Kjersti Erichsen, Elin Inderhaug, Morten Mattingsdal et al. · European Journal of Neurology · 2007 · 31 citations