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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|January 25, 2013
[Electromyography (EMG) and neurography in patients with severe neuromuscular diseases]Sissel Løseth, Torberg TorbergsenTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|September 14, 2010
[Intravenous IgG for treatment of neuromuscular diseases]Christian A Vedeler, Svein Ivar Mellgren, Roald Omdal, et al.Muscle & Nerve|June 17, 2015
Painful cramps and giant myotonic discharges in a family with the Nav1.4-G1306A mutationTorberg Torbergsen, Karin Jurkat-Rott, Erik V Stålberg, et al.Journal of Neuromuscular Diseases|November 19, 2016
A de novo Mutation in the SCN4A Gene Causing Sodium Channel MyotoniaKristin Ørstavik, Sean Ciaran Wallace, Torberg Torbergsen, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 28, 2002
The myotonia congenita mutation A331T confers a novel hyperpolarization-activated gate to the muscle chloride channel ClC-1Maike Warnstedt, Chen Sun, Barbara Poser, et al.Neuromuscular Disorders : NMD|October 22, 2010
Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2IEva Stensland, Sigurd Lindal, Christoffer Jonsrud, et al.Journal of Neurology|January 19, 2013
A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) geneSissel Løseth, Nicol C Voermans, Torberg Torbergsen, et al.Annals of Neurology|April 1, 2003
Homozygous mutations in caveolin-3 cause a severe form of rippling muscle diseaseChristian Kubisch, Benedikt G H Schoser, Monika von Düring, et al.Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.Pageof 1