Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sissel, Løseth"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Creatine kinase (CK) has been associated with neuropathy, but the mechanisms are uncertain. We hypothesized that peripheral nerve function is impaired in subjects with persistent CK elevation (hyperCKemia) compared to age- and sex matched co
Externí odkaz:
https://doaj.org/article/9917a7e6317a432fb6ef6fc4293bbeef
Autor:
Trond Sand, Kristian Bernhard Nilsen, Øystein Dunker, Martin Uglem, Marie Bu Kvaløy, Sissel Løseth, Ina Elen Hjelland, Sara Maria Allen, Maria Dehli Vigeland, Inge Petter Kleggetveit
Publikováno v:
BMJ Open Diabetes Research & Care, Vol 11, Iss 6 (2023)
Introduction There is a need for simple and cheap diagnostic tools for diabetic polyneuropathy (DPN). We aimed to assess the diagnostic accuracy of the 5.07/10 g monofilament test in patients referred to polyneuropathy assessments, as well as to exam
Externí odkaz:
https://doaj.org/article/6224d648da5342968d5ff91f05cf91ac
Autor:
Gro Solbakken, Sissel Løseth, Anne Froholdt, Torunn D. Eikeland, Terje Nærland, Jan C. Frich, Espen Dietrichs, Kristin Ørstavik
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Background Pain is prevalent in myotonic dystrophy 1 (DM1). This study investigated whether CTG repeat size, disease duration, BMI and motor and psychological function were related to pain in adult patients with DM1, and if there were gender
Externí odkaz:
https://doaj.org/article/9c6347f5061e471284afb98867651984
Autor:
Sissel Løseth, Helle Høyer, Kim-Mai Le, Eric Delpire, Einar Kinge, Asgeir Lande, Hilde Tveitan Hilmarsen, Toril Fagerheim, Øivind Nilssen, Geir Julius Braathen
Publikováno v:
Brain. 146:912-922
We describe five families from different regions in Norway with a late-onset autosomal-dominant hereditary polyneuropathy sharing a heterozygous variant in the SLC12A6 gene. Mutations in the same gene have previously been described in infants with au
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 136(12-13)
Around 700 people in Norway have myasthenia gravis, an autoimmune disease that affects neuromuscular transmission and results in fluctuating weakness in some muscles as its sole symptom. The diagnosis is based on typical symptoms and findings, detect
Publikováno v:
Tidsskrift for Den norske legeforening. 136
Autor:
Torberg, Torbergsen, Karin, Jurkat-Rott, Erik V, Stålberg, Sissel, Løseth, Anne, Hødneø, Frank, Lehmann-Horn
Publikováno v:
Musclenerve. 52(4)
Two previously reported Norwegian patients with painful muscle cramps and giant myotonic discharges were genotyped and compared with those of members of 21 families harboring the same mutation.Using primers specific for SCN4A and CLCN1, the DNA of th
Autor:
Sissel, Løseth, Erik V, Stålberg, Sigurd, Lindal, Edel, Olsen, Rolf, Jorde, Svein I, Mellgren
Publikováno v:
Journal of the peripheral nervous system : JPNS. 21(1)
The purpose of this study was to evaluate progression of diabetic polyneuropathy and differences in the spectrum and evolution of large- and small-fiber involvement in patients with diabetes type 1 and 2 over 5 years. Fifty-nine patients (35 type 1 a
Autor:
Sissel, Løseth, Torberg, Torbergsen
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 133(2)
Many neuromuscular diseases are potentially severe, and EMG and neurography are methods used in the assessment of these conditions.The article is based on the authors' knowledge and experience, with special emphasis on the use of these methods in the