Lindal S - Search Results

1

Clinical and muscle biopsy findings in Norwegian paediatric patients with limb girdle muscular dystrophy 2I.

Rasmussen M, Scheie D, Breivik N, Mork M, Lindal S. Rasmussen M, et al. Among authors: lindal s. Acta Paediatr. 2014 May;103(5):553-8. doi: 10.1111/apa.12561. Epub 2014 Feb 10. Acta Paediatr. 2014. PMID: 24447024

2

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

3

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

4

Muscle biopsies in children--an evaluation of histopathology and clinical value during a 5-year period.

Skram MK, Gulati S, Larsson E, Lindal S, Torp SH. Skram MK, et al. Among authors: lindal s. Ups J Med Sci. 2009;114(1):41-5. doi: 10.1080/03009730802604949. Ups J Med Sci. 2009. PMID: 19242871 Free PMC article.

5

Statin-associated myopathy with normal creatine kinase levels. Case report from a Norwegian family.

Trøseid M, Henriksen OA, Lindal S. Trøseid M, et al. Among authors: lindal s. APMIS. 2005 Sep;113(9):635-7. doi: 10.1111/j.1600-0463.2005.apm_270.x. APMIS. 2005. PMID: 16218940

Troseid M, Henriksen OA, Lindal S. Statin-associated myopathy with normal creatine kinase levels - case report from a Norwegian family. ...

Troseid M, Henriksen OA, Lindal S. Statin-associated myopathy with normal creatine kinase levels - case report from a Norwegia …

6

A new congenital myopathy in a Norwegian family.

Aurivillius M, Lindal S. Aurivillius M, et al. Among authors: lindal s. Acta Paediatr. 2001 Dec;90(12):1478-80. doi: 10.1080/08035250152708923. Acta Paediatr. 2001. PMID: 11853349

7

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

8

Early mitochondrial changes in chronic progressive ocular myopathy.

Aasly J, Lindal S, Torbergsen T, Borud O, Mellgren SI. Aasly J, et al. Among authors: lindal s. Eur Neurol. 1990;30(6):314-8. doi: 10.1159/000117363. Eur Neurol. 1990. PMID: 1963142

9

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

10

Focal myositis--neurogenic phenomenon?

Lunde HM, Skeie GO, Bertelsen AK, Karlsen B, Miletic H, Lindal S, Brautaset NJ, Bindoff LA. Lunde HM, et al. Among authors: lindal s. Neuromuscul Disord. 2012 Apr;22(4):350-4. doi: 10.1016/j.nmd.2011.10.023. Epub 2011 Dec 9. Neuromuscul Disord. 2012. PMID: 22153989

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