Protocolo diagnóstico de hipercolesterolemias

M. Pocovi Mieras1, P. Mata López2, P. Cia Gómez3
1Departamento de Bioquímica, Biología Molecular y Celular. Facultad de Ciencias de Zaragoza. Zaragoza
2Unidad de Lípidos Fundación Jiménez Díaz. Madrid
3Servicio de Medicina Interna y Unidad de Hipertensión arterial y Riesgo vascular. Hospital Clínico Universitario Lozano Blesa. Zaragoza

Tài liệu tham khảo

Koivisto, 1992, Diagnosis of heterozygous familial hypercholesterolemia. DNA analysis complements clinical examination and analysis of serum lipid levels, Arterioscler Thromb, 12, 584, 10.1161/01.ATV.12.5.584 Umans-Eckenhausen, 2001, Review of first 5 years of screening for familial hypercholesterolemia in Netherlands, Lancet, 357, 165, 10.1016/S0140-6736(00)03587-X WHO. Human Genetic Program. Familial Hypercholesterolemia, report of a WHO consultation. WHO/HGN/FH/CONS/98.7 Paris, October 1997. 2004, Guidelines for the Management of heterozygous Familial Hypercholesterolemia, Atherosclerosis, 173, 55, 10.1016/j.atherosclerosis.2003.11.010