Vitenskapelige artikler

2015

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.
J Peripher Nerv Syst. 2015 Dec 13. doi: 10.1111/jns.12154. [Epub ahead of print]

PMID: 26663481

Stålberg E, Sanders DB, Ali S, Cooray G, Leonardis L, Löseth S, Machado F, Maldonado A, Martinez-Aparicio C, Sandberg A, Smith B, Widenfalk J, Kouyoumdjian JA.
Muscle Nerve. 2015 Jun 25. doi: 10.1002/mus.24750. [Epub ahead of print]

PMID:26112058

Torbergsen T, Jurkat-Rott K, Stålberg EV, Løseth S, Hødneø A, Lehmann-Horn F.
Muscle Nerve. 2015 Oct;52(4):680-3. doi: 10.1002/mus.24672. Epub 2015 Jun 30.

PMID: 26080010

Zaharieva IT, Thor MG, Oates EC, van Karnebeek C, Hendson G, Blom E, Witting N, Rasmussen M, Gabbett MT, Ravenscroft G, Sframeli M, Suetterlin K, Sarkozy A, D'Argenzio L, Hartley L, Matthews E, Pitt M, Vissing J, Ballegaard M, Krarup C, Slørdahl A, Halvorsen H, Ye XC, Zhang LH, Løkken N, Werlauff U, Abdelsayed M, Davis MR, Feng L, Phadke R, Sewry CA, Morgan JE, Laing NG, Vallance H, Ruben P, Hanna MG, Lewis S, Kamsteeg EJ, Männikkö R, Muntoni F.
Brain. 2015 Dec 22. pii: awv352. [Epub ahead of print]

PMID: 26700687 Free Article

Johnsen SH, Lilleng H, Bekkelund SI.
J Clin Hypertens (Greenwich). 2015 Apr;17(4):323. doi: 10.1111/jch.12488. Epub 2015 Jan 27. No abstract available.

PMID: 25625689


 2014

Segregation analysis in families with Charcot-Marie-Tooth disease allows reclassification of putative disease causing mutations.

Østern R, Fagerheim T, Hjellnes H, Nygård B, Mellgren SI, Nilssen Ø.
BMC Med Genet.
2014 Jan 21;15:12. doi: 10.1186/1471-2350-15-12.PMID: 24444136

Small nerve fiber involvement is frequent in X-linked adrenoleukodystrophy.

Horn MA, Nilsen KB, Jørum E, Mellgren SI, Tallaksen CM.
Neurology. 2014 May 13;82(19):1678-83. doi: 10.1212/WNL.0000000000000415. Epub 2014 Apr 9.PMID: 4719486

Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy.

Nicole S, Chaouch A, Torbergsen T, Bauché S, de Bruyckere E, Fontenille MJ, Horn MA, van Ghelue M, Løseth S, Issop Y, Cox D, Müller JS, Evangelista T, Stålberg E, Ioos C, Barois A, Brochier G, Sternberg D, Fournier E, Hantaï D, Abicht A, Dusl M, Laval SH, Griffin H, Eymard B, Lochmüller H.
Brain. 2014 Sep;137(Pt 9):2429-43. doi: 10.1093/brain/awu160. Epub 2014 Jun 20. PMID: 24951643

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.
Acta Paediatr.
2014 May;103(5):553-8. doi: 10.1111/apa.12561. Epub 2014 Feb 10. PMID:24447024

 


2013

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.
Neuromuscul Disord. 2013 Jan;23(1):29-35. doi: 10.1016/j.nmd.2012.07.008. Epub 2012 Sep 8.PMID:22967790

Cardiac resynchronization therapy improves minute ventilation/carbon dioxide production slope and skeletal muscle capillary density without reversal of skeletal muscle pathology or inflammation.

Larsen AI, Lindal S, Myreng K, Ogne C, Kvaløy JT, Munk PS, Aukrust P, Yndestad A, Dickstein K, Nilsen DW.
Europace. 2013 Jun;15(6):857-64. doi: 10.1093/europace/eus428. Epub 2013 Jan 15.PMID:23322010

Electromyography (EMG) and neurography in patients with severe neuromuscular diseases].

Løseth S, Torbergsen T.
Tidsskr Nor Laegeforen.
2013 Jan 22;133(2):174-8. doi: 10.4045/tidsskr.12.0184. Review. Norwegian. PMID:23344603

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.
J Neurol. 2013 Jun;260(6):1504-10. doi: 10.1007/s00415-012-6817-7. Epub 2013 Jan 18.PMID:23329375

A man in his 60s with chest pain and pareses.

Müller KI, Devik K, Vorren T, Johnsen SH.
Tidsskr Nor Laegeforen. 2013 Jun 25;133(12-13):1320-4. doi: 10.4045/tidsskr.12.0979.
English, Norwegian. No abstract available. PMID:23817263

Diagnostic laboratory testing for Charcot Marie Tooth disease (CMT): the spectrum of gene defects in Norwegian patients with CMT and its implications for future genetic test strategies.

Ostern R, Fagerheim T, Hjellnes H, Nygård B, Mellgren SI, Nilssen O.
BMC Med Genet.
2013 Sep 21;14:94. doi: 10.1186/1471-2350-14-94. PMID:24053775

Small- and large-fiber neuropathy after 40 years of type 1 diabetes: associations with glycemic control and advanced protein glycation: the Oslo Study.

Sveen KA, Karimé B, Jørum E, Mellgren SI, Fagerland MW, Monnier VM, Dahl-Jørgensen K, Hanssen KF.
Diabetes Care. 2013 Nov;36(11):3712-7. doi: 10.2337/dc13-0788. Epub 2013 Sep 11. PMID:24026557

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The cutaneous nerve biopsy: technical aspects, indications, and contribution.

Mellgren SI, Nolano M, Sommer C.
Handb Clin Neurol.
2013;115:171-88. doi: 10.1016/B978-0-444-52902-2.00010-2. PMID:23931780

[Electromyography (EMG) and neurography in patients with severe neuromuscular diseases].

Løseth S, Torbergsen T.
Tidsskr Nor Laegeforen.
2013 Jan 22;133(2):174-8. doi: 10.4045/tidsskr.12.0184. Review. Norwegian. PMID:23344603