A Tybjaerg Hansen - JoVE Visualize

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Atherosclerosis|August 1, 1991

Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemiaP Talmud, A Tybjaerg-Hansen, D Bhatnagar, et al.

Annals of Internal Medicine|September 1, 1997

ACE gene polymorphism as a risk factor for ischemic cerebrovascular diseaseB Agerholm-Larsen, A Tybjaerg-Hansen, R Frikke-Schmidt, et al.

Human Genetics|May 1, 1992

Multipoint linkage analysis of the short arm of chromosome 11 in non-insulin dependent diabetes including maturity onset diabetes of youthS O'Rahilly, P Patel, O J Lehmann, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999

Mutations in the lipoprotein lipase gene associated with ischemic heart disease in men. The Copenhagen city heart studyH H Wittrup, A Tybjaerg-Hansen, R Steffensen, et al.

Diabetes|August 1, 1992

Linkage analysis of maturity-onset diabetes of the young with microsatellite polymorphisms. No linkage to ADA or GLUT2 genes in two familiesP Patel, Y M Lo, A Hattersley, et al.

The Journal of Clinical Endocrinology and Metabolism|December 17, 1997

Studies of genetic variability of the uncoupling protein 1 gene in Caucasian subjects with juvenile-onset obesityS A Urhammer, M Fridberg, T I Sørensen, et al.

Diabetologia|March 14, 1998

Organisation of the coding exons and mutational screening of the uncoupling protein 3 gene in subjects with juvenile-onset obesityS A Urhammer, L T Dalgaard, T I Sørensen, et al.

Biochemical and Biophysical Research Communications|April 7, 1997

Amino acid variants in the human leptin receptor: lack of association to juvenile onset obesityS M Echwald, T D Sørensen, T I Sørensen, et al.

International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|April 1, 1997

Identification of two novel missense mutations in the human OB geneS M Echwald, S B Rasmussen, T I Sørensen, et al.

Atherosclerosis|January 1, 1990

Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten casesA Tybjaerg-Hansen, J Gallagher, J Vincent, et al.

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Showing results (51-60 of 68) with videos related to

Sort By:

Pageof 7

Atherosclerosis|August 1, 1991

Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemiaP Talmud, A Tybjaerg-Hansen, D Bhatnagar, et al.

Annals of Internal Medicine|September 1, 1997

ACE gene polymorphism as a risk factor for ischemic cerebrovascular diseaseB Agerholm-Larsen, A Tybjaerg-Hansen, R Frikke-Schmidt, et al.

Human Genetics|May 1, 1992

Multipoint linkage analysis of the short arm of chromosome 11 in non-insulin dependent diabetes including maturity onset diabetes of youthS O'Rahilly, P Patel, O J Lehmann, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999

Mutations in the lipoprotein lipase gene associated with ischemic heart disease in men. The Copenhagen city heart studyH H Wittrup, A Tybjaerg-Hansen, R Steffensen, et al.

Diabetes|August 1, 1992

Linkage analysis of maturity-onset diabetes of the young with microsatellite polymorphisms. No linkage to ADA or GLUT2 genes in two familiesP Patel, Y M Lo, A Hattersley, et al.

The Journal of Clinical Endocrinology and Metabolism|December 17, 1997

Studies of genetic variability of the uncoupling protein 1 gene in Caucasian subjects with juvenile-onset obesityS A Urhammer, M Fridberg, T I Sørensen, et al.

Diabetologia|March 14, 1998

Organisation of the coding exons and mutational screening of the uncoupling protein 3 gene in subjects with juvenile-onset obesityS A Urhammer, L T Dalgaard, T I Sørensen, et al.

Biochemical and Biophysical Research Communications|April 7, 1997

Amino acid variants in the human leptin receptor: lack of association to juvenile onset obesityS M Echwald, T D Sørensen, T I Sørensen, et al.

International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|April 1, 1997

Identification of two novel missense mutations in the human OB geneS M Echwald, S B Rasmussen, T I Sørensen, et al.

Atherosclerosis|January 1, 1990

Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten casesA Tybjaerg-Hansen, J Gallagher, J Vincent, et al.

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