Diagnóstico de la hipercolesterolemia familiar. Un paso adelante

作者: F. Civeira , M. Pocoví

DOI: 10.1016/S0214-9168(02)78844-X

关键词: Medicine

摘要:

参考文章(6)
P V Koivisto, U M Koivisto, T A Miettinen, K Kontula, Diagnosis of heterozygous familial hypercholesterolemia. DNA analysis complements clinical examination and analysis of serum lipid levels. Arteriosclerosis, Thrombosis, and Vascular Biology. ,vol. 12, pp. 584- 592 ,(1992) , 10.1161/01.ATV.12.5.584
P H Pritchard, J S Hill, M R Hayden, J Frohlich, Genetic and environmental factors affecting the incidence of coronary artery disease in heterozygous familial hypercholesterolemia. Arteriosclerosis, Thrombosis, and Vascular Biology. ,vol. 11, pp. 290- 297 ,(1991) , 10.1161/01.ATV.11.2.290
G Schmitz, T Brüning, E Kovacs, S Barlage, Fluorescence flow cytometry of human leukocytes in the detection of LDL receptor defects in the differential diagnosis of hypercholesterolemia. Arteriosclerosis, Thrombosis, and Vascular Biology. ,vol. 13, pp. 1053- 1065 ,(1993) , 10.1161/01.ATV.13.7.1053
Eric J.G Sijbrands, Rudi G.J Westendorp, M Paola Lombardi, Louis M Havekes, Rune R Frants, John J.P Kastelein, Augustinus H.M Smelt, Additional risk factors influence excess mortality in heterozygous familial hypercholesterolaemia. Atherosclerosis. ,vol. 149, pp. 421- 425 ,(2000) , 10.1016/S0021-9150(99)00336-6
Rodrigo Alonso, Sergio Castillo, Fernando Civeira, José Puzo, Juan José de la Cruz, Miguel Pocoví, Pedro Mata, Hipercolesterolemia familiar heterocigota en España. Estudio descriptivo de 819 casos no relacionados Medicina Clinica. ,vol. 118, pp. 487- 492 ,(2002) , 10.1016/S0025-7753(02)72428-7