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H Gylling

Showing results (61-70 of 132) with videos related to

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Atherosclerosis|November 1, 1989
Apolipoprotein E phenotype and cholesterol metabolism in familial hypercholesterolemiaH Gylling, T Kuusi, H Vanhanen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|September 1, 1992
Cholesterol absorption, elimination, and synthesis related to LDL kinetics during varying fat intake in men with different apoprotein E phenotypesT A Miettinen, H Gylling, H Vanhanen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|May 1, 1994
Regulation of serum cholesterol level in middle-aged and elderly men. Relation of cholesterol absorption and synthesis to lipoprotein metabolismH Gylling, T Strandberg, R Tilvis, et al.
BMJ (Clinical Research Ed.)|April 29, 1998
Baseline serum cholestanol as predictor of recurrent coronary events in subgroup of Scandinavian simvastatin survival study. Finnish 4S InvestigatorsT A Miettinen, H Gylling, T Strandberg, et al.
Journal of Lipid Research|April 7, 1999
Serum sterols during stanol ester feeding in a mildly hypercholesterolemic populationH Gylling, P Puska, E Vartiainen, et al.
FEBS Letters|March 28, 1988
Identification of a deletion in the LDL receptor gene. A Finnish type of mutationK Aalto-Setälä, H Gylling, T Miettinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|August 17, 2002
[Diagnostics of Smith-Lemli-Opitz syndrome with the help of gas chromatography]M Nissinen, H Gylling, M Kaski, et al.
The American Journal of Clinical Nutrition|June 29, 2000
Introducing a new component of the metabolic syndrome: low cholesterol absorptionP Simonen, H Gylling, A N Howard, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|November 15, 2000
Postprandial retinyl palmitate and squalene metabolism is age dependentH Relas, H Gylling, R A Rajaratnam, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 1, 1997
Familial moderate hypercholesterolemia caused by Asp235-->Glu mutation of the LDL receptor gene and co-occurrence of a de novo deletion of the LDL receptor gene in the same familyU M Koivisto, H Gylling, T A Miettinen, et al.
Pageof 14

Showing results (61-70 of 132) with videos related to

Sort By:
Pageof 14
Atherosclerosis|November 1, 1989
Apolipoprotein E phenotype and cholesterol metabolism in familial hypercholesterolemiaH Gylling, T Kuusi, H Vanhanen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|September 1, 1992
Cholesterol absorption, elimination, and synthesis related to LDL kinetics during varying fat intake in men with different apoprotein E phenotypesT A Miettinen, H Gylling, H Vanhanen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|May 1, 1994
Regulation of serum cholesterol level in middle-aged and elderly men. Relation of cholesterol absorption and synthesis to lipoprotein metabolismH Gylling, T Strandberg, R Tilvis, et al.
BMJ (Clinical Research Ed.)|April 29, 1998
Baseline serum cholestanol as predictor of recurrent coronary events in subgroup of Scandinavian simvastatin survival study. Finnish 4S InvestigatorsT A Miettinen, H Gylling, T Strandberg, et al.
Journal of Lipid Research|April 7, 1999
Serum sterols during stanol ester feeding in a mildly hypercholesterolemic populationH Gylling, P Puska, E Vartiainen, et al.
FEBS Letters|March 28, 1988
Identification of a deletion in the LDL receptor gene. A Finnish type of mutationK Aalto-Setälä, H Gylling, T Miettinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|August 17, 2002
[Diagnostics of Smith-Lemli-Opitz syndrome with the help of gas chromatography]M Nissinen, H Gylling, M Kaski, et al.
The American Journal of Clinical Nutrition|June 29, 2000
Introducing a new component of the metabolic syndrome: low cholesterol absorptionP Simonen, H Gylling, A N Howard, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|November 15, 2000
Postprandial retinyl palmitate and squalene metabolism is age dependentH Relas, H Gylling, R A Rajaratnam, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 1, 1997
Familial moderate hypercholesterolemia caused by Asp235-->Glu mutation of the LDL receptor gene and co-occurrence of a de novo deletion of the LDL receptor gene in the same familyU M Koivisto, H Gylling, T A Miettinen, et al.
Pageof 14