T. Torbergsen
Oslo University Hospital(NO)University Hospital of North Norway(NO)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Ion channel regulation and function, Cardiomyopathy and Myosin Studies, Peripheral Neuropathies and Disorders
Most-Cited Works
- → Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease(2001)210 cited
- → Andrology: Mitochondrial disease and reduced sperm motility(1993)195 cited
- → Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia(2001)102 cited
- → Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy(2014)100 cited
- → A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene(2013)94 cited
- → Pre‐Eclampsia‐A Mitochondrial Disease?(1989)86 cited
- → Homozygous mutations in caveolin‐3 cause a severe form of rippling muscle disease