Jeanette Koht

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

Mathieu Anheim, B. Monga, Marie‐Céline Fleury et al. · Brain · 2009 · 242 citations · Full text

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

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene

Domitille Gras, Laurence Jonard, Emmanuel Roze et al. · Journal of Neurology Neurosurgery & Psychiatry · 2012 · 124 citations

Prevalence and etiology of epilepsy in a <scp>N</scp>orwegian county—A population based study

Marte Syvertsen, Karl O. Nakken, Astrid Edland et al. · Epilepsia · 2015 · 95 citations · Full text

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