[Homozygote familial hypercholesterinemia. Pathophysiology and genetic control of cholesterol metabolism]
- PMID: 207958
[Homozygote familial hypercholesterinemia. Pathophysiology and genetic control of cholesterol metabolism]
Similar articles
-
Familial hypercholesterolemia: A genetic defect in the low-density lipoprotein receptor.N Engl J Med. 1976 Jun 17;294(25):1386-90. doi: 10.1056/NEJM197606172942509. N Engl J Med. 1976. PMID: 177875 No abstract available.
-
Characterization of hepatic low density lipoprotein binding and cholesterol metabolism in normal and homozygous familial hypercholesterolemic subjects.J Clin Invest. 1984 Feb;73(2):429-36. doi: 10.1172/JCI111229. J Clin Invest. 1984. PMID: 6321555 Free PMC article.
-
The LDL pathway in human fibroblasts: a receptor-mediated mechanism for the regulation of cholesterol metabolism.Curr Top Cell Regul. 1976;11:147-81. doi: 10.1016/b978-0-12-152811-9.50011-0. Curr Top Cell Regul. 1976. PMID: 187385 Review. No abstract available.
-
The effect of portacaval shunt on hepatic lipoprotein metabolism in familial hypercholesterolemia.J Surg Res. 1985 Nov;39(5):369-77. doi: 10.1016/0022-4804(85)90090-3. J Surg Res. 1985. PMID: 4057999
-
[Molecular pathophysiology of familial hypercholesterolemia].Pol Tyg Lek. 1985 Dec 16;40(50):1407-10. Pol Tyg Lek. 1985. PMID: 3913938 Review. Polish. No abstract available.