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Genetic aspects of restenosis after percutaneous coronary interventions: Towards more tailored therapyAGEMA, W. R. P; JUKEMA, J. W; PIMSTONE, S. N et al.European heart journal. 2001, Vol 22, Num 22, pp 2058-2074, issn 0195-668XArticle

Phenotypic variation in heterozygous familial hypercholesterolemia : A comparison of Chinese patients with the same or similar mutations in the LDL receptor gene in China or CanadaPIMSTONE, S. N; SUN, X.-M; DU SOUICH, C et al.Arteriosclerosis, thrombosis, and vascular biology. 1998, Vol 18, Num 2, pp 309-315, issn 1079-5642Article

Human Mendelian pain disorders: a key to discovery and validation of novel analgesicsGOLDBERG, Y. P; PIMSTONE, S. N; NAMDARI, R et al.Clinical genetics. 2012, Vol 82, Num 4, pp 367-373, issn 0009-9163, 7 p.Article

Differences in the phenotype between children with Familial defective apolipoprotein B-100 and Familial hypercholesterolemiaPIMSTONE, S. N; DEFESCHE, J. C; CLEE, S. M et al.Arteriosclerosis, thrombosis, and vascular biology. 1997, Vol 17, Num 5, pp 826-833, issn 1079-5642Article

A common truncation variant of lipoprotein lipase (Ser447X) confers protection against coronary heart disease : the Framingham Offspring StudyGAGNE, S. E; LARSON, M. G; PIMSTONE, S. N et al.Clinical genetics. 1999, Vol 55, Num 6, pp 450-454, issn 0009-9163Article

A frequent mutation in the lipoprotein lipase gene (D9N) deteriorates the biochemical and clinical phenotype of familial hypercholesterolemiaWITTEKOEK, M. E; MOLL, E; PIMSTONE, S. N et al.Arteriosclerosis, thrombosis, and vascular biology. 1999, Vol 19, Num 11, pp 2708-2713, issn 1079-5642Article

A common mutation in the lipoprotein lipase gene (N291S) alters the lipoprotein phenotype and risk for cardiovascular disease in patients with familial hypercholesterolemiaWITTEKOEK, M. E; PIMSTONE, S. N; REYMER, P. W. A et al.Circulation (New York, N.Y.). 1998, Vol 97, Num 8, pp 729-735, issn 0009-7322Article

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Mutations in the gene for lipoprotein lipase : a cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemiaPIMSTONE, S. N; GAGNE, S. E; MOORJANI, S et al.Arteriosclerosis, thrombosis, and vascular biology. 1995, Vol 15, Num 10, pp 1704-1712, issn 1079-5642Article

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Loss-of-function mutations in the Na_v1.7 gene underlie congenital indifference to pain in multiple human populationsGOLDBERG, Y. P; MACFARLANE, J; PAYNE, B et al.Clinical genetics. 2007, Vol 71, Num 4, pp 311-319, issn 0009-9163, 9 p.Article