Magnhild Rasmussen

Oslo, Norway

Last Updated: 09/26/2026

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Found 44 publications

Liver Involvement in POLG Disease-a Multicentre Cohort Study of 202 Patients.

Liver Involvement in POLG Disease-a Multicentre Cohort Study of 202 Patients.

Journal: Journal of inherited metabolic disease
Published: June 02, 2025

Type 1 spinal muscular atrophy treated with nusinersen in Norway, a five-year follow-up.

Type 1 spinal muscular atrophy treated with nusinersen in Norway, a five-year follow-up.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: July 04, 2024

Correction: Myotonic dystrophy type 1 – a multiorgan disorder

Correction: Myotonic dystrophy type 1 – a multiorgan disorder

Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: May 13, 2024

Myotonic dystrophy type 1 - a multiorgan disorder.

Myotonic dystrophy type 1 - a multiorgan disorder.

Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: April 23, 2024

Status epilepticus in POLG disease: a large multinational study.

Status epilepticus in POLG disease: a large multinational study.

Journal: Journal of neurology
Published: March 27, 2024

Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study.

Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study.

Journal: Annals of clinical and translational neurology
Published: February 06, 2024

Start and stop criteria for very costly medicines – the example of spinal muscular atrophy

Start and stop criteria for very costly medicines – the example of spinal muscular atrophy

Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: October 13, 2023

Cognitive function, behaviour and quality of life in children with myotonic dystrophy type 1 in South - Eastern Norway.

Cognitive function, behaviour and quality of life in children with myotonic dystrophy type 1 in South - Eastern Norway.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: December 22, 2022

Epidemiology and natural history in 101 subjects with FKRP-related limb-girdle muscular dystrophy R9. The Norwegian LGMDR9 cohort study (2020).

Epidemiology and natural history in 101 subjects with FKRP-related limb-girdle muscular dystrophy R9. The Norwegian LGMDR9 cohort study (2020).

Journal: Neuromuscular disorders : NMD
Published: February 22, 2022

Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency.

Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency.

Journal: JIMD reports
Published: December 19, 2021

Priority setting at the clinical level: the case of nusinersen and the Norwegian national expert group.

Priority setting at the clinical level: the case of nusinersen and the Norwegian national expert group.

Journal: BMC medical ethics
Published: March 09, 2021

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
Showing 1-12 of 44

Last Updated: 09/26/2026