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Arve Dahl

Showing results (11-20 of 17) with videos related to

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Journal of Neurology|February 1, 2011
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patientOdile Dubourg, Thierry Maisonobe, Anthony Behin, et al.
Neuromuscular Disorders : NMD|April 6, 2012
Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 geneRune Østern, Toril Fagerheim, Kristin Ørstavik, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 2, 2004
[Treatment of patients with neuromuscular disease in a warm climate]Arve Dahl, Ola H Skjeldal, Andreas Simensen, et al.
Stroke|August 30, 2008
Soluble CD36 in plasma is increased in patients with symptomatic atherosclerotic carotid plaques and is related to plaque instabilityAase Handberg, Mona Skjelland, Annika E Michelsen, et al.
Atherosclerosis|June 15, 2007
Plasma levels of granzyme B are increased in patients with lipid-rich carotid plaques as determined by echogenicityMona Skjelland, Annika E Michelsen, Kirsten Krohg-Sørensen, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
Circulation|February 7, 2007
Increased expression of visfatin in macrophages of human unstable carotid and coronary atherosclerosis: possible role in inflammation and plaque destabilizationTuva B Dahl, Arne Yndestad, Mona Skjelland, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Journal of Neurology|February 1, 2011
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patientOdile Dubourg, Thierry Maisonobe, Anthony Behin, et al.
Neuromuscular Disorders : NMD|April 6, 2012
Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 geneRune Østern, Toril Fagerheim, Kristin Ørstavik, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 2, 2004
[Treatment of patients with neuromuscular disease in a warm climate]Arve Dahl, Ola H Skjeldal, Andreas Simensen, et al.
Stroke|August 30, 2008
Soluble CD36 in plasma is increased in patients with symptomatic atherosclerotic carotid plaques and is related to plaque instabilityAase Handberg, Mona Skjelland, Annika E Michelsen, et al.
Atherosclerosis|June 15, 2007
Plasma levels of granzyme B are increased in patients with lipid-rich carotid plaques as determined by echogenicityMona Skjelland, Annika E Michelsen, Kirsten Krohg-Sørensen, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
Circulation|February 7, 2007
Increased expression of visfatin in macrophages of human unstable carotid and coronary atherosclerosis: possible role in inflammation and plaque destabilizationTuva B Dahl, Arne Yndestad, Mona Skjelland, et al.
Pageof 2