Anne-sofie V. Eisum
Copenhagen, Denmark
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Structural changes and contractility in muscle assessed by magnetic resonance imaging in individuals with ryanodine receptor 1-related rhabdomyolysis or myalgia.
Journal: Muscle & nerve
Published: March 15, 2024
Hypokalemic periodic paralysis: a 3-year follow-up study.
Journal: Journal of neurology
Published: May 22, 2023
Quantitative Muscle MRI and Clinical Findings in Women With Pathogenic Dystrophin Gene Variants.
Journal: Frontiers in neurology
Published: May 10, 2021
Energy metabolism during exercise in patients with β-enolase deficiency (GSDXIII).
Journal: JIMD reports
Published: February 09, 2021
Prolonged fasting-induced hyperketosis, hypoglycaemia and impaired fat oxidation in child and adult patients with spinal muscular atrophy type II.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: January 08, 2021
Contractile properties are impaired in congenital myopathies.
Journal: Neuromuscular disorders : NMD
Published: February 13, 2020
Growth and differentiation factor 15 as a biomarker for mitochondrial myopathy.
Journal: Mitochondrion
Published: June 02, 2019
Permanent muscle weakness in hypokalemic periodic paralysis.
Journal: Neurology
Published: April 12, 2019
Fat oxidation is impaired during exercise in lipin-1 deficiency.
Journal: Neurology
Published: February 13, 2019
Expanding the phenotype of filamin-C-related myofibrillar myopathy.
Journal: Clinical neurology and neurosurgery
Published: September 12, 2018
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: September 04, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026