Freja Fornander
Copenhagen, Denmark
Last Updated: 09/26/2026
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Found 14 publications
Muscle involvement in women carrying pathogenic DMD gene variants: A 6.5-year follow-up study.
Journal: Journal of neuromuscular diseases
Published: January 09, 2026
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
Three novel FHL1 variants cause a mild phenotype of Emery-Dreifuss muscular dystrophy.
Journal: Human mutation
Published: November 26, 2021
Cardiac Involvement in Women With Pathogenic Dystrophin Gene Variants.
Journal: Frontiers in neurology
Published: May 10, 2021
Quantitative Muscle MRI and Clinical Findings in Women With Pathogenic Dystrophin Gene Variants.
Journal: Frontiers in neurology
Published: May 10, 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
Evaluation of inflammatory lesions over 2 years in facioscapulohumeral muscular dystrophy.
Journal: Neurology
Published: March 21, 2019
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: September 04, 2018
Last Updated: 09/26/2026