Lindal S - Search Results

1

Variation of serum creatine kinase (CK) levels and prevalence of persistent hyperCKemia in a Norwegian normal population. The Tromsø Study.

Lilleng H, Abeler K, Johnsen SH, Stensland E, Løseth S, Jorde R, Figenschau Y, Lindal S, Wilsgaard T, Bekkelund SI. Lilleng H, et al. Among authors: lindal s. Neuromuscul Disord. 2011 Jul;21(7):494-500. doi: 10.1016/j.nmd.2011.04.007. Epub 2011 May 17. Neuromuscul Disord. 2011. PMID: 21592795

2

Clinical impact of persistent hyperCKemia in a Norwegian general population: a case-control study.

Lilleng H, Abeler K, Johnsen SH, Stensland E, Løseth S, Lindal S, Wilsgaard T, Bekkelund SI. Lilleng H, et al. Among authors: lindal s. Neuromuscul Disord. 2013 Jan;23(1):29-35. doi: 10.1016/j.nmd.2012.07.008. Epub 2012 Sep 8. Neuromuscul Disord. 2013. PMID: 22967790

3

Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2I.

Stensland E, Lindal S, Jonsrud C, Torbergsen T, Bindoff LA, Rasmussen M, Dahl A, Thyssen F, Nilssen Ø. Stensland E, et al. Among authors: lindal s. Neuromuscul Disord. 2011 Jan;21(1):41-6. doi: 10.1016/j.nmd.2010.08.008. Epub 2010 Oct 18. Neuromuscul Disord. 2011. PMID: 20961759

4

Polyneuropathy in type 1 and type 2 diabetes: comparison of nerve conduction studies, thermal perception thresholds and intraepidermal nerve fibre densities.

Løseth S, Mellgren SI, Jorde R, Lindal S, Stålberg E. Løseth S, et al. Among authors: lindal s. Diabetes Metab Res Rev. 2010 Feb;26(2):100-6. doi: 10.1002/dmrr.1049. Diabetes Metab Res Rev. 2010. PMID: 19943330

5

Limb girdle muscular dystrophy type 2I: No correlation between clinical severity, histopathology and glycosylated α-dystroglycan levels in patients homozygous for common FKRP mutation.

Alhamidi M, Brox V, Stensland E, Liset M, Lindal S, Nilssen Ø. Alhamidi M, et al. Among authors: lindal s. Neuromuscul Disord. 2017 Jul;27(7):619-626. doi: 10.1016/j.nmd.2017.02.015. Epub 2017 Mar 4. Neuromuscul Disord. 2017. PMID: 28479227

6

Small and large fiber neuropathy in those with type 1 and type 2 diabetes: a 5-year follow-up study.

Løseth S, Stålberg EV, Lindal S, Olsen E, Jorde R, Mellgren SI. Løseth S, et al. Among authors: lindal s. J Peripher Nerv Syst. 2016 Mar;21(1):15-21. doi: 10.1111/jns.12154. J Peripher Nerv Syst. 2016. PMID: 26663481

7

The value of skin biopsy with recording of intraepidermal nerve fiber density and quantitative sensory testing in the assessment of small fiber involvement in patients with different causes of polyneuropathy.

Nebuchennykh M, Løseth S, Lindal S, Mellgren SI. Nebuchennykh M, et al. Among authors: lindal s. J Neurol. 2009 Jul;256(7):1067-75. doi: 10.1007/s00415-009-5065-y. Epub 2009 Mar 1. J Neurol. 2009. PMID: 19252773

8

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 SI. Løseth S, et al. Among authors: lindal s. Eur J Neurol. 2006 Feb;13(2):105-11. doi: 10.1111/j.1468-1331.2006.01232.x. Eur J Neurol. 2006. PMID: 16490039

9

Human leukocyte antigen class I in polymyositis: leukocyte infiltrates, regeneration, and impulse block.

Fladby T, Kampman MT, Løseth S, Lindal S, Mellgren SI. Fladby T, et al. Among authors: lindal s. Muscle Nerve. 1997 Dec;20(12):1534-40. doi: 10.1002/(sici)1097-4598(199712)20:12<1534::aid-mus8>3.0.co;2-9. Muscle Nerve. 1997. PMID: 9390666

10

A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene.

Løseth S, Voermans NC, Torbergsen T, Lillis S, Jonsrud C, Lindal S, Kamsteeg EJ, Lammens M, Broman M, Dekomien G, Maddison P, Muntoni F, Sewry C, Radunovic A, de Visser M, Straub V, van Engelen B, Jungbluth H. Løseth S, et al. Among authors: lindal s. J Neurol. 2013 Jun;260(6):1504-10. doi: 10.1007/s00415-012-6817-7. Epub 2013 Jan 18. J Neurol. 2013. PMID: 23329375

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