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Klaus Brusgaard

Showing results (11-20 of 94) with videos related to

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Journal of Clinical Lipidology|December 3, 2010
New mutations in APOB100 involved in familial hypobetalipoproteinemiaKlaus Brusgaard, Lars Kjaersgaard, Anne-Birthe Bo Hansen, et al.
Ugeskrift for Laeger|March 10, 2023
Stine Bjørn Gram, Klaus Brusgaard, Lilian Bomme Ousager, et al.
Clinical Case Reports|January 7, 2016
Case report: vitamin D-dependent rickets type 1 caused by a novel CYP27B1 mutationLaila Füchtbauer, Klaus Brusgaard, Pål Ledaal, et al.
Molecular Genetics & Genomic Medicine|December 16, 2017
ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasiaPernille M Tørring, Anette D Kjeldsen, Lilian Bomme Ousager, et al.
Diabetes|September 28, 2005
Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinismKhalid Hussain, Joseph Bryan, Henrick T Christesen, et al.
Molecular and Cellular Endocrinology|September 6, 2011
Vitamin D and diabetes: its importance for beta cell and immune functionHeidi Wolden-Kirk, Lut Overbergh, Henrik Thybo Christesen, et al.
The Journal of Dermatology|March 25, 2024
Plantar keratoderma and curly hair as a diagnostic clue of cardiomyopathy riskStine Bjørn Gram, Klaus Brusgaard, Anette Bygum, et al.
Molecular Genetics and Genomics : MGG|June 20, 2020
A novel gene in early childhood diabetes: EDEM2 silencing decreases SLC2A2 and PXD1 expression, leading to impaired insulin secretionYazeid Alhaidan, Henrik Thybo Christesen, Kurt Højlund, et al.
Calcified Tissue International|August 2, 2022
Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial DiseaseSimone Rask Nielsen, Stinus Gadegaard Hansen, Claus Bistrup, et al.
Ugeskrift for Laeger|November 29, 2011
[Congenital hyperinsulinism--new causes and clinical variations]Maria Fuglsang Bruun, Stine Hedegaard Christoffersen, Klaus Brusgaard, et al.
Pageof 10

Showing results (11-20 of 94) with videos related to

Sort By:
Pageof 10
Journal of Clinical Lipidology|December 3, 2010
New mutations in APOB100 involved in familial hypobetalipoproteinemiaKlaus Brusgaard, Lars Kjaersgaard, Anne-Birthe Bo Hansen, et al.
Ugeskrift for Laeger|March 10, 2023
Stine Bjørn Gram, Klaus Brusgaard, Lilian Bomme Ousager, et al.
Clinical Case Reports|January 7, 2016
Case report: vitamin D-dependent rickets type 1 caused by a novel CYP27B1 mutationLaila Füchtbauer, Klaus Brusgaard, Pål Ledaal, et al.
Molecular Genetics & Genomic Medicine|December 16, 2017
ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasiaPernille M Tørring, Anette D Kjeldsen, Lilian Bomme Ousager, et al.
Diabetes|September 28, 2005
Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinismKhalid Hussain, Joseph Bryan, Henrick T Christesen, et al.
Molecular and Cellular Endocrinology|September 6, 2011
Vitamin D and diabetes: its importance for beta cell and immune functionHeidi Wolden-Kirk, Lut Overbergh, Henrik Thybo Christesen, et al.
The Journal of Dermatology|March 25, 2024
Plantar keratoderma and curly hair as a diagnostic clue of cardiomyopathy riskStine Bjørn Gram, Klaus Brusgaard, Anette Bygum, et al.
Molecular Genetics and Genomics : MGG|June 20, 2020
A novel gene in early childhood diabetes: EDEM2 silencing decreases SLC2A2 and PXD1 expression, leading to impaired insulin secretionYazeid Alhaidan, Henrik Thybo Christesen, Kurt Højlund, et al.
Calcified Tissue International|August 2, 2022
Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial DiseaseSimone Rask Nielsen, Stinus Gadegaard Hansen, Claus Bistrup, et al.
Ugeskrift for Laeger|November 29, 2011
[Congenital hyperinsulinism--new causes and clinical variations]Maria Fuglsang Bruun, Stine Hedegaard Christoffersen, Klaus Brusgaard, et al.
Pageof 10