Chantal E. Tallaksen

Oslo, Norway

Last Updated: 09/26/2026

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Found 48 publications

Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult-Onset Degenerative Ataxia.

Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult-Onset Degenerative Ataxia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 12, 2022

The impact of gender, puberty, and pregnancy in patients with POLG disease.

The impact of gender, puberty, and pregnancy in patients with POLG disease.

Journal: Annals of clinical and translational neurology

Published: July 16, 2020

Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5.

Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5.

Journal: Journal of the neurological sciences

Published: June 23, 2020

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis.

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis.

Journal: Brain : a journal of neurology

Published: March 09, 2019

Fever-related ataxia: a case report of CAPOS syndrome.

Fever-related ataxia: a case report of CAPOS syndrome.

Journal: Cerebellum & ataxias

Published: October 23, 2018

Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex.

Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex.

Journal: Brain : a journal of neurology

Published: August 06, 2018

Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy.

Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy.

Journal: Muscle & nerve

Published: May 29, 2018

Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications.

Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications.

Journal: Epilepsia

Published: May 24, 2018

Homocarnosinosis: A historical update and findings in the SPG11 gene.

Homocarnosinosis: A historical update and findings in the SPG11 gene.

Journal: Acta neurologica Scandinavica

Published: April 10, 2018

Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.

Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.

Journal: JAMA neurology

Published: February 27, 2018

Charcot-Marie-Tooth disease type 4C in Norway: Clinical characteristics, mutation spectrum and minimum prevalence.

Charcot-Marie-Tooth disease type 4C in Norway: Clinical characteristics, mutation spectrum and minimum prevalence.

Journal: Neuromuscular disorders : NMD

Published: January 12, 2018

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.

Journal: PloS one

Published: October 13, 2017

Showing 1-12 of 48

Last Updated: 09/26/2026