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The effect of age and gender on epidermal nerve fiber density

Neurology, 2004-03, Vol.62 (5), p.774

2004

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ID 390 – Association between intraepidermal nerve fiber density and quantitative sensory testing in the patients with possible small fiber neuropathy

Clinical neurophysiology, 2016-03, Vol.127 (3), p.e58-e58

2016

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P612: Small and large fibre neuropathy in patients with diabetes type 1 compared with type 2: a follow-up study

Clinical neurophysiology, 2014-06, Vol.125, p.S215-S215

2014

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Intraepidermal nerve fibre density, quantitative sensory testing and nerve conduction studies in a patient material with symptoms and signs of sensory polyneuropathy

European journal of neurology, 2006-02, Vol.13 (2), p.105-111

2006

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Nerve biopsy - some comments on procedures and indications

Acta neurologica Scandinavica, 2011-08, Vol.124 (s191), p.64-70

2011

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G.P.277

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.900-900

2014

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P.8.1 Muscle biopsy findings in Limb Girdle muscle Dystrophy 2I (LGMD2I)

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.779-780

2013

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CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S232-S233

2015

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Pregnancy protects against antiangiogenic and fibrogenic effects of angiotensin II in rat hearts

Acta Physiologica, 2011-04, Vol.201 (4), p.445-456

2011

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Good outcome in a patient treated for cerebral amyloid angiopathy presenting as an expansive process with inflammation and contrast enhancement

American journal of neuroradiology : AJNR, 2011-04, Vol.32 (4), p.E75-E75

2011

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P2.17 Fukutin-related protein resides in the Golgi cisternae of human skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction interface

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.665-666

2011

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P3.43 An adult-onset, slowly progressive axial myopathy with cataracts due to mutations in the skeletal muscle ryanodine receptor (RYR1) gene

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.695-695

2011

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P2.19 Norwegian patients with Limb Girdle Muscular Dystrophy 2I structural changes and immunhistochemistry related to clinical findings and genotype–fenotype

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.666-666

2011

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Morphologic changes in tubular cells from in situ kidneys following experimental hypothermia and rewarming

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2005-01, Vol.113 (1), p.13-20

2005

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Gene Expression, Function and Ischemia Tolerance in Male and Female Rat Hearts After Sub-Toxic Levels of Angiotensin II

Cardiovascular toxicology, 2011-03, Vol.11 (1), p.38-47

2011

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G.P.17.05 Creatine kinase (CK) in a normal population: Towards new referent values?

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.656-656

2009

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EM.P.2.09 Spectrum of mutations and phenotypic variability in FKRP-related disease in Norway

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.554-554

2009

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Altered Brain Myelin Sheath Morphology after Rewarming in Situ

Ultrastructural pathology, 2010, Vol.34 (2), p.82-89

2010

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Event Reconstruction Performance of the ALICE High Level Trigger for + Collisions

IEEE transactions on nuclear science, 2011-08, Vol.58 (4), p.1706-1713

2011

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G.P.19.05 Statin associated myopathy with normal creatine kinase levels: Case report from a Norwegian family

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.895-895

2007

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Does imprint cytology of brain tumours improve intraoperative diagnoses?

Acta neurologica Scandinavica, 2003-09, Vol.108 (3), p.153-156

2003

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A new congenital myopathy in a Norwegian family

Acta Paediatrica, 2001-12, Vol.90 (12), p.1478-1480

2001

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Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S109

2017

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P.36 - Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S109-S109

2017

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Nerve biopsy - some comments on procedures and indications: Nerve biopsy

Acta neurologica Scandinavica, 2011-08, Vol.124, p.64-70

2011

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The effect of age and gender on epidermal nerve fiber density

ID 390 – Association between intraepidermal nerve fiber density and quantitative sensory testing in the patients with possible small fiber neuropathy

P612: Small and large fibre neuropathy in patients with diabetes type 1 compared with type 2: a follow-up study

Intraepidermal nerve fibre density, quantitative sensory testing and nerve conduction studies in a patient material with symptoms and signs of sensory polyneuropathy

Nerve biopsy - some comments on procedures and indications

G.P.277

P.8.1 Muscle biopsy findings in Limb Girdle muscle Dystrophy 2I (LGMD2I)

CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy

Pregnancy protects against antiangiogenic and fibrogenic effects of angiotensin II in rat hearts

Good outcome in a patient treated for cerebral amyloid angiopathy presenting as an expansive process with inflammation and contrast enhancement

P2.17 Fukutin-related protein resides in the Golgi cisternae of human skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction interface

P3.43 An adult-onset, slowly progressive axial myopathy with cataracts due to mutations in the skeletal muscle ryanodine receptor (RYR1) gene

P2.19 Norwegian patients with Limb Girdle Muscular Dystrophy 2I structural changes and immunhistochemistry related to clinical findings and genotype–fenotype

Morphologic changes in tubular cells from in situ kidneys following experimental hypothermia and rewarming

Gene Expression, Function and Ischemia Tolerance in Male and Female Rat Hearts After Sub-Toxic Levels of Angiotensin II

G.P.17.05 Creatine kinase (CK) in a normal population: Towards new referent values?

EM.P.2.09 Spectrum of mutations and phenotypic variability in FKRP-related disease in Norway

Altered Brain Myelin Sheath Morphology after Rewarming in Situ

Event Reconstruction Performance of the ALICE High Level Trigger for + Collisions

G.P.19.05 Statin associated myopathy with normal creatine kinase levels: Case report from a Norwegian family

Does imprint cytology of brain tumours improve intraoperative diagnoses?

A new congenital myopathy in a Norwegian family

Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

P.36 - Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

Nerve biopsy - some comments on procedures and indications: Nerve biopsy

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