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Human Genetics|August 1, 1993
Screening for point mutations in exon 10 of the low density lipoprotein receptor gene by analysis of single-strand conformation polymorphisms: detection of a nonsense mutation-FH469-->StopT P Leren, K Solberg, O K Rødningen, et al.
Archives of Disease in Childhood|September 28, 2011
Paediatric screening for hypercholesterolaemia in EuropeD M Kusters, C de Beaufort, K Widhalm, et al.
Metabolism: Clinical and Experimental|November 1, 1995
Comparison of the effect of fluvastatin, an hydroxymethyl glutaryl coenzyme A reductase inhibitor, and cholestyramine, a bile acid sequestrant, on lipoprotein particles defined by apolipoprotein compositionJ M Bard, J Dallongeville, E Hagen, et al.
Human Genetics|June 1, 1995
Screening for known mutations in the LDL receptor gene causing familial hypercholesterolemiaT P Leren, H Sundvold, O K Rødningen, et al.
Clinical Genetics|November 1, 1992
A new polymorphism in exon 11 of the LDL receptor gene in healthy people and in familial hypercholesterolemia subjectsT P Leren, K Solberg, O Røsby, et al.
European Journal of Clinical Pharmacology|January 1, 1992
Short-term effects of treatment with simvastatin on testicular function in patients with heterozygous familial hypercholesterolaemiaK Purvis, A Tollefsrud, H Rui, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|May 1, 1991
Dietary n-6 fatty acids inhibit the incorporation of dietary n-3 fatty acids in thrombocyte and serum phospholipids in humans: a controlled dietetic studyM Grønn, C Gørbitz, E Christensen, et al.
Journal of Lipid Research|July 1, 1996
Effect of homocysteine on copper ion-catalyzed, azo compound-initiated, and mononuclear cell-mediated oxidative modification of low density lipoproteinB Halvorsen, I Brude, C A Drevon, et al.
Metabolism: Clinical and Experimental|November 1, 1996
The effect of growth hormone on low-density lipoprotein cholesterol and lipoprotein (a) levels in familial hypercholesterolemiaS Tonstad, E Sundt, L Ose, et al.
The Journal of Pediatrics|January 1, 1977
A heritable syndrome of craniosynostosis, short thin hair, dental abnormalities, and short limbs: cranioectodermal dysplasiaL S Levin, J C Perrin, L Ose, et al.
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