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Martin Prøven Bogsrud

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Atherosclerosis|March 19, 2021
Molecular genetic testing for autosomal dominant hypercholesterolemia in 29,449 Norwegian index patients and 14,230 relatives during the years 1993-2020Trond P Leren, Martin Prøven Bogsrud
Current Opinion in Lipidology|August 9, 2022
Cascade screening for familial hypercholesterolemia should be organized at a national levelTrond P Leren, Martin Prøven Bogsrud
Journal of Clinical Lipidology|September 4, 2021
The importance of cascade genetic screening for diagnosing autosomal dominant hypercholesterolemia: Results from twenty years of a national screening program in NorwayTrond P Leren, Martin Prøven Bogsrud
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|June 16, 2007
[Practical advice for registration of clinical trials]Martin Prøven Bogsrud, Aksel Sogstad, Kjetil Retterstøl
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 3, 2013
[Treatment with statins]Martin Prøven Bogsrud, Åsmund Reikvam, Kjetil Retterstøl
European Heart Journal|March 4, 2026
What is the correct screening method for FH, depends on what you aim to findMartin Prøven Bogsrud, Knut Erik Berge, Kirsten B Holven
European Journal of Preventive Cardiology|June 2, 2022
Molecular genetics in 4408 cardiomyopathy probands and 3008 relatives in Norway: 17 years of genetic testing in a national laboratoryTonje Talsnes Stava, Trond P Leren, Martin Prøven Bogsrud
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|March 24, 2017
A physically fit woman in her thirties with exertional dyspnoeaMartin Prøven Bogsrud, Asgeir Græsdal, Kjetil Retterstøl, et al.
Journal of Clinical Lipidology|November 19, 2023
Molecular genetic testing and measurement of levels of GPIHBP1 autoantibodies in patients with severe hypertriglyceridemia: The importance of identifying the underlying cause of hypertriglyceridemiaThea Bismo Strøm, Anders Aune Tveita, Martin Prøven Bogsrud, et al.
Journal of Human Genetics|August 13, 2010
Analysis of LDLR mRNA in patients with familial hypercholesterolemia revealed a novel mutation in intron 14, which activates a cryptic splice siteMari Ann Kulseth, Knut Erik Berge, Martin Prøven Bogsrud, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Atherosclerosis|March 19, 2021
Molecular genetic testing for autosomal dominant hypercholesterolemia in 29,449 Norwegian index patients and 14,230 relatives during the years 1993-2020Trond P Leren, Martin Prøven Bogsrud
Current Opinion in Lipidology|August 9, 2022
Cascade screening for familial hypercholesterolemia should be organized at a national levelTrond P Leren, Martin Prøven Bogsrud
Journal of Clinical Lipidology|September 4, 2021
The importance of cascade genetic screening for diagnosing autosomal dominant hypercholesterolemia: Results from twenty years of a national screening program in NorwayTrond P Leren, Martin Prøven Bogsrud
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|June 16, 2007
[Practical advice for registration of clinical trials]Martin Prøven Bogsrud, Aksel Sogstad, Kjetil Retterstøl
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 3, 2013
[Treatment with statins]Martin Prøven Bogsrud, Åsmund Reikvam, Kjetil Retterstøl
European Heart Journal|March 4, 2026
What is the correct screening method for FH, depends on what you aim to findMartin Prøven Bogsrud, Knut Erik Berge, Kirsten B Holven
European Journal of Preventive Cardiology|June 2, 2022
Molecular genetics in 4408 cardiomyopathy probands and 3008 relatives in Norway: 17 years of genetic testing in a national laboratoryTonje Talsnes Stava, Trond P Leren, Martin Prøven Bogsrud
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|March 24, 2017
A physically fit woman in her thirties with exertional dyspnoeaMartin Prøven Bogsrud, Asgeir Græsdal, Kjetil Retterstøl, et al.
Journal of Clinical Lipidology|November 19, 2023
Molecular genetic testing and measurement of levels of GPIHBP1 autoantibodies in patients with severe hypertriglyceridemia: The importance of identifying the underlying cause of hypertriglyceridemiaThea Bismo Strøm, Anders Aune Tveita, Martin Prøven Bogsrud, et al.
Journal of Human Genetics|August 13, 2010
Analysis of LDLR mRNA in patients with familial hypercholesterolemia revealed a novel mutation in intron 14, which activates a cryptic splice siteMari Ann Kulseth, Knut Erik Berge, Martin Prøven Bogsrud, et al.
Pageof 4