CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy
Van Ghelue, M, Wahl, C, Arntzen, K, Loseth, S, Bindoff, L, Sveberg, L, Rosby, O, Popperud, T, Rasmussen, M, Halvorsen, H, Lindal, S, Jonsrud, C, Orstavik, K
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Quantitative sensory testing in patients with polyneuropathy and healthy individuals
Nebuchennykh, M., Løseth, S., Stålberg, E., Mellgren, S. I.
Published in Acta neurologica Scandinavica (01.05.2008)
Published in Acta neurologica Scandinavica (01.05.2008)
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Conference Proceeding
Peripheral neuropathy caused by severe hypothermia
Løseth, S, Bågenholm, A, Torbergsen, T, Stålberg, E
Published in Clinical neurophysiology (01.05.2013)
Published in Clinical neurophysiology (01.05.2013)
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Aspects of peripheral nerve involvement in patients with treated hypothyroidism
Nebuchennykh, M., Løseth, S., Mellgren, S. I.
Published in European journal of neurology (01.01.2010)
Published in European journal of neurology (01.01.2010)
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Intraepidermal nerve fibre density, quantitative sensory testing and nerve conduction studies in a patient material with symptoms and signs of sensory polyneuropathy
Løseth, S., Lindal, S., Stålberg, E., Mellgren, S. I.
Published in European journal of neurology (01.02.2006)
Published in European journal of neurology (01.02.2006)
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P612: Small and large fibre neuropathy in patients with diabetes type 1 compared with type 2: a follow-up study
Løseth, S, Stålberg, E, Lindal, S, Jorde, R, Mellgren, S.I
Published in Clinical neurophysiology (01.06.2014)
Published in Clinical neurophysiology (01.06.2014)
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Idiopathic polyneuropathy and impaired glucose metabolism in a Norwegian patient series
Nebuchennykh, M., Løseth, S., Jorde, R., Mellgren, S. I.
Published in European journal of neurology (01.08.2008)
Published in European journal of neurology (01.08.2008)
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MYOFIBRILLAR AND DISTAL MYOPATHIES
Orstavik, K., Almaas, V., Rasmussen, M., Jonsrud, C., Jensen, S., Loseth, S., Leren, T.
Published in Neuromuscular disorders : NMD (01.10.2018)
Published in Neuromuscular disorders : NMD (01.10.2018)
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MYOFIBRILLAR AND DISTAL MYOPATHIES: P.249A novel mutation in MYH7 giving rise to different phenotypes in a mother and her daughter
Orstavik, K., Almaas, V., Rasmussen, M., Jonsrud, C., Jensen, S., Loseth, S., Leren, T.
Published in Neuromuscular disorders : NMD (01.10.2018)
Published in Neuromuscular disorders : NMD (01.10.2018)
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P.8.1 Muscle biopsy findings in Limb Girdle muscle Dystrophy 2I (LGMD2I)
Lindal, S, Myreng, K, Løseth, S, Jonsrud, C, Alhamidi, M, Stensland, E, Nilssen, Ø
Published in Neuromuscular disorders : NMD (01.10.2013)
Published in Neuromuscular disorders : NMD (01.10.2013)
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Reference values for jitter recorded by concentric needle electrodes in healthy controls: A multicenter study
Stålberg, Erik, Sanders, Donald B., Ali, Sajjad, Cooray, Gerald, Leonardis, Lea, Löseth, Sissel, Machado, Flavia, Maldonado, Antonio, Martinez-Aparicio, Carmen, Sandberg, Arne, Smith, Benn, Widenfalk, Johan, Aris Kouyoumdjian, João
Published in Muscle & nerve (01.03.2016)
Published in Muscle & nerve (01.03.2016)
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Mutations in anoctamin 5 in limb girdle muscular dystrophy in Norway: Phenotypic variability and mutation spectrum
Van Ghelue, M, Arntzen, K.A, Halvorsen, H, Ingebrigtsen, M, Skogstad, A, Hestholm, B, Løseth, S, Mellgren, S.I, Rasmussen, F, Lindahl, S, Jonsrud, C
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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