Familial hypercholesterolaemia

Frederickson D.S. Plasma lipid abnormalities and cutaneous and subcutaneous xanthomas. In: Fitzpatrick T.B. , ed. Dermatology in General Medicine. New York: McGraw-Hill, 1979: 1112–25

Brown M.S. , Goldstein J.L. Receptor mediated control of cholesterol metabolism. Science 1976; 191: 150–3

West R. , Gibson P. , Lloyd J. Treatment of homozygous familial hypercholesterolaemia: an informative sibship. Br Med J 1985; 291: 1079–80

Thompson G.R. , Lowenthal R. , Myant N.B. Plasma exchange in the management of homozygous familial hypercholesterolaemia. Lancet 1975; i: 1208–11

Thompson G.R. , Miller J.P. , Breslow J.L. Improved survival of patients with homozygous familial hypercholesterolaemia treated with plasma exchange. Br Med J 1985; 291: 1671–3

Starzl T.H. , Chase H.P. , Ahrens E.H. Portacaval shunt in patient with familial hypercholesterolaemia. Ann Surg 1983; 198: 273–81

Bilheimer D.W. , Goldstein J.L. , Grundy S.M. , Starzl T.E. , Brown M.S. Liver transplantation to provide low density lipoprotein receptors and lower plasma cholesterol in a child with homozygous familial hypercholesterolaemia. N Engl J Med 1984; 311: 1658–63