Phytosterolaemia in three unrelated South African families.

Author:

Berger G. M.,Deppe W. M.,Marais A. D.,Biggs M.

Publisher

BMJ

Subject

General Medicine

Reference28 articles.

1. P-Sitosterolaemia and xanthomatosis. A newly described lipid storage disease in two sisters;Bhattacharyya, A.K.; Connor, W.E.;J Clin Invest,1974

2. Salen, G., Shefer, S., Nguyen, L., Ness, G.C., Tint, G.S. & Shore, V. Sitosterolaemia. J Lipid Res 1992, 33: 945-955.

3. Familial diseases with storage of sterols other than cholesterol: cerebrotendinous xanthomatosis and phytosterolaemia;Bjorkhem, I.; Skrede, S.,1989

4. A unique patient with coexisting cerebrotendinous xanthomatosis and P-sitosterolaemia;C., Wang; Lin, H.J.; Chan, T.-K.; Salen, G.; Chan, W.-C.; Tse, T.-F.;Am J Med,1981

5. Familial phytosterolaemia: cholestanolaemia and abnormal bile composition;Khachadurian, A.K.; Salen, G.;Clin Res,1980

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