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Magnhild Rasmussen

Showing results (21-30 of 47) with videos related to

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Neuromuscular Disorders : NMD|October 22, 2010
Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2IEva Stensland, Sigurd Lindal, Christoffer Jonsrud, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 13, 2024
Kristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 23, 2024
Myotonic dystrophy type 1 - a multiorgan disorderKristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
Journal of Inherited Metabolic Disease|September 28, 2017
Erratum to: The presence of anaemia negatively influences survival in patients with POLG diseaseOmar Hikmat, Charalampos Tzoulis, Claus Klingenberg, et al.
Journal of Inherited Metabolic Disease|September 3, 2017
The presence of anaemia negatively influences survival in patients with POLG diseaseOmar Hikmat, Charalampos Tzoulis, Claus Klingenberg, et al.
Annals of Clinical and Translational Neurology|June 7, 2024
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort studyErle Kristensen, Linda Mathisen, Siren Berland, et al.
The Annals of Thoracic Surgery|September 25, 2007
Clinical and psychosocial follow-up study of children treated with extracorporeal membrane oxygenationKari Wagner, Ivar Risnes, Torhild Berntsen, et al.
JIMD Reports|April 18, 2022
Novel mutations in the <i>HADHB</i> gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiencyKristin Ørstavik, Kjell Arne Arntzen, Per Mathisen, et al.
Mitochondrion|September 25, 2020
Mental health and health related quality of life in mitochondrial POLG diseaseOmar Hikmat, Bente Johanne Vederhus, Merete Roineland Benestad, et al.
Neuromuscular Disorders : NMD|July 25, 2016
Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2Christeen Ramane J Pedurupillay, Silja S Amundsen, Tuva Barøy, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Neuromuscular Disorders : NMD|October 22, 2010
Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2IEva Stensland, Sigurd Lindal, Christoffer Jonsrud, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 13, 2024
Kristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 23, 2024
Myotonic dystrophy type 1 - a multiorgan disorderKristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
Journal of Inherited Metabolic Disease|September 28, 2017
Erratum to: The presence of anaemia negatively influences survival in patients with POLG diseaseOmar Hikmat, Charalampos Tzoulis, Claus Klingenberg, et al.
Journal of Inherited Metabolic Disease|September 3, 2017
The presence of anaemia negatively influences survival in patients with POLG diseaseOmar Hikmat, Charalampos Tzoulis, Claus Klingenberg, et al.
Annals of Clinical and Translational Neurology|June 7, 2024
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort studyErle Kristensen, Linda Mathisen, Siren Berland, et al.
The Annals of Thoracic Surgery|September 25, 2007
Clinical and psychosocial follow-up study of children treated with extracorporeal membrane oxygenationKari Wagner, Ivar Risnes, Torhild Berntsen, et al.
JIMD Reports|April 18, 2022
Novel mutations in the <i>HADHB</i> gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiencyKristin Ørstavik, Kjell Arne Arntzen, Per Mathisen, et al.
Mitochondrion|September 25, 2020
Mental health and health related quality of life in mitochondrial POLG diseaseOmar Hikmat, Bente Johanne Vederhus, Merete Roineland Benestad, et al.
Neuromuscular Disorders : NMD|July 25, 2016
Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2Christeen Ramane J Pedurupillay, Silja S Amundsen, Tuva Barøy, et al.
Pageof 5