Vitenskapelige artikler i 2011

 Lunde Hanne Marie Bøe, Skeie Geir Olve, Bertelsen Anne K, Karlsen Bjørn, Miletic Hrvoje, Lindal Sigurd, Brautaset Nils J, Bindoff Laurence A
Focal myositis - A neurogenic phenomenon?
Neuromuscul Disord 2011 Dec. Epub 2011 des 8
PMID: 22153989

 Sun C, Van Ghelue M, Tranebjærg L, Thyssen F, Nilssen Ø, Torbergsen T
Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
Clin Genet 2011 Dec;80(6):574-80. Epub 2011 jan 19
PMID: 21204798

 Lilleng Hallvard, Johnsen Stein Harald, Wilsgaard Tom, Bekkelund Svein Ivar
Are the currently used reference intervals for creatine kinase (CK) reflecting the general population? The Troms? Study.
Clin Chem Lab Med 2011 Nov. Epub 2011 nov 10
PMID: 22070220

Johnsen Stein H, Lilleng Hallvard, Wilsgaard Tom, Bekkelund Svein I
Creatine kinase activity and blood pressure in a normal population: the Tromsø study.
J Hypertens 2011 Jan;29(1):36-42.
PMID: 21063205

Lilleng Hallvard, Abeler Karin, Johnsen Stein H, Stensland Eva, Løseth Sissel, Jorde Rolf, Figenschau Yngve, Lindal Sigurd, Wilsgaard Tom, Bekkelund Svein I
Variation of serum creatine kinase (CK) levels and prevalence of persistent hyperCKemia in a Norwegian normal population. The Tromsø Study.
Neuromuscul Disord 2011 Jul;21(7):494-500. Epub 2011 mai 17
PMID: 21592795

Alhamidi Maisoon, Kjeldsen Buvang Elisabeth, Fagerheim Toril, Brox Vigdis, Lindal Sigurd, Van Ghelue Marijke, Nilssen Øivind
Fukutin-related protein resides in the Golgi cisternae of skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction.
PLoS One 2011;6(8):e22968. Epub 2011 aug 23
PMID: 21886772

Stensland Eva, Lindal Sigurd, Jonsrud Christoffer, Torbergsen Torberg, Bindoff Laurence A, Rasmussen Magnhild, Dahl Arve, Thyssen Frances, Nilssen Øivind
Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2I.
Neuromuscul Disord 2011 Jan;21(1):41-6. Epub 2010 okt 18
PMID: 20961759

 Mellgren S I, Lindal S
Nerve biopsy--some comments on procedures and indications.
Acta Neurol Scand Suppl 2011.
PMID: 21711259
 

Marijke Van Ghelue
Hva skjer innen nyere forskning i Duchenne/Becker muskeldystrofi?
Habiliteringstjenestens 20 års jubileum. September 2011, Tromsø (foredrag)

Marijke Van Ghelue
Hva skjer innen nyere forskning?
Muskelseminar for foreldre og lokale hjelpeapparat, Januar 2011, Tromsø (foredrag)

Wahl CM, Arntzen KA, Løseth S, Glad R, Fagerheim T, Van Ghelue M, Jonsrud C, Lindal S
ANO5-relatert LGMD: hyppig årsak til LGMD i Norge?
Fagkonferanse om nevromuskulære sykdommer, Oktober 2011 Tromsø (foredrag)

Wahl CM, Fagerheim T, Van Ghelue M, Jonsrud C, Lindal S
Myopati med nemaline legemer og hørselstap hos to søstre
Fagkonferanse om nevromuskulære sykdommer, Oktober 2011 Tromsø (foredrag)

Lindal S, Stensland E, Jonsrud C, Torbergsen T, Myreng K, Bindoff LA, Rasmussen M, Thyssen F, Nilssen Ø
Norwegian patiens with LGMD 2I structural changes and immunhistochemistry related to clinical findings and genotype-fenotype
World Muscle society Meeting September 2011 Almancil Portugal (poster)

Løseth S, Lillis S, Torbergsen T, Jonsrud C, Lindal S, Madisson P, Muntoni F, Sewry C, Abbs S, Straub V, Jungbluth H
An adult-onset, slowly progressive axial myopathy with cataracts due to mutations in the skeletar muscle ryanodine receptor gene
World Muscle society Meeting September 2011 Almancil Portugal (poster)
 

Løseth S, Lillis S, Torbergsen T, Jonsrud C, Lindal S, Madisson P, Muntoni F, Sewry C, Abbs S, Straub V, Jungbluth H
An adult-onset, slowly progressive axial myopathy with cataracts due to mutations in the skeletar muscle ryanodine receptor gene
Neuromuscular Disorders, Volume 21, Issues 9-10, October 2011, Page 695

Lindal S, Stensland E, Jonsrud C, Torbergsen T, Myreng K, Bindoff LA, Rasmussen M, Thyssen F, Nilssen Ø
Norwegian patiens with LGMD 2I structural changes and immunhistochemistry related to clinical findings and genotype-fenotype
Neuromuscular Disorders, Volume 21, Issues 9-10, October 2011, Page 666

Alhamidi Maisoon, Buvang Elisabeth Kjeldsen, Fagerheim Toril, Brox Vigdis, Lindal Sigurd, Van Ghelue Marijke, Nilssen Øivind
Fukutin-related protein resides in the Golgi cisternae of human skeletal muscle forms homodimers via an N-terminal interaction
World Muscle society Meeting September 2011 Almancil Portugal (poster)

Van Ghelue Marijke, Alhamidi Maisoon, Buvang Elisabeth Kjeldsen, Fagerheim Toril, Brox Vigdis, Lindal Sigurd, Nilssen Øivind
Fukutin-related protein localized in the Golgi cisternae of human skeletal muscle forms homodimers via an N-terminal interaction
NSHG (Norsk Selskap for Human Genetikk) November 2011 Bergen (poster)

Van Ghelue Marijke, Alhamidi Maisoon, Buvang Elisabeth Kjeldsen, Fagerheim Toril, Brox Vigdis, Lindal Sigurd, Nilssen Øivind
Fukutin-related protein localized in the Golgi cisternae of human skeletal muscle forms homodimers via an N-terminal interaction
Functional genomics and system biology. November 2011 Cambridge, UK (poster)