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5. Metabolic effects of portacaval shunt surgery and liver transplantation in familial hypercholesterolemia. Bilheimer DW Beitr Infusionsther; 1988; 23():61-73. PubMed ID: 2484783 [No Abstract] [Full Text] [Related]
6. Prospects for gene therapy of familial hypercholesterolemia. Wilson JM; Chowdhury JR Mol Biol Med; 1990 Jun; 7(3):223-32. PubMed ID: 2215209 [TBL] [Abstract][Full Text] [Related]
7. Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemia. Feussner G; Dobmeyer J; Nissen H; Hansen TS Am J Med Genet; 1996 Oct; 65(2):149-54. PubMed ID: 8911609 [TBL] [Abstract][Full Text] [Related]
8. Pseudohomozygous type II hyperlipoproteinemia. Fujita M; Okamoto S; Shirai K; Saito Y; Yoshida S Dermatologica; 1991; 182(2):94-7. PubMed ID: 2050241 [TBL] [Abstract][Full Text] [Related]
9. Familial hypercholesterolemia: a genetic receptor disease. Goldstein JL; Brown MS Hosp Pract (Off Ed); 1985 Nov; 20(11):35-41, 45-6. PubMed ID: 3932389 [No Abstract] [Full Text] [Related]
10. [Lipoprotein receptors and dyslipoproteinemias]. Orbetsova V Vutr Boles; 1984; 23(3):1-7. PubMed ID: 6087571 [No Abstract] [Full Text] [Related]
11. Biochemical genetics of LDL receptor mutations in familial hypercholesterolemia. Goldstein JL; Kottke BA; Brown MS Prog Clin Biol Res; 1982; 103 Pt B():161-76. PubMed ID: 6298809 [No Abstract] [Full Text] [Related]
12. Low-density lipoprotein receptor deficiency resulting in familial hypercholesterolaemia in a black man. A follow-up study. Coetzee GA; van Wingerden JJ; van der Westhuyzen DR S Afr Med J; 1985 Feb; 67(7):259-61. PubMed ID: 3983774 [TBL] [Abstract][Full Text] [Related]
13. A xanthomatosis-susceptibility gene may exist in a Syrian family with familial hypercholesterolemia. Vergopoulos A; Bajari T; Jouma M; Knoblauch H; Aydin A; Bähring S; Mueller-Myhsok B; Dresel A; Joubran R; Luft FC; Schuster H Eur J Hum Genet; 1997; 5(5):315-23. PubMed ID: 9412789 [TBL] [Abstract][Full Text] [Related]
14. Clinical studies in a kindred with a kinetic LDL receptor mutation causing familial hypercholesterolemia. Bilheimer DW; East C; Grundy SM; Nora JJ Am J Med Genet; 1985 Nov; 22(3):593-8. PubMed ID: 4061492 [TBL] [Abstract][Full Text] [Related]
15. [Familial disorders of lipid metabolism in childhood]. Herrmann W; Biermann J Z Arztl Fortbild (Jena); 1986; 80(17):725-8. PubMed ID: 3811401 [No Abstract] [Full Text] [Related]
16. [Homozygous familial hypercholesterolemia (author's transl)]. Nervi F; Arteaga A; Maiz A; Tocornal J; Severin MC Rev Med Chil; 1979 Jul; 107(7):624-8. PubMed ID: 232560 [No Abstract] [Full Text] [Related]
17. [Catabolism of low-density lipoproteins via receptors and its regulation]. Mazière JC; Mazière C; Gardette J; Polonovski J Ann Biol Clin (Paris); 1986; 44(5):545-50. PubMed ID: 3544977 [TBL] [Abstract][Full Text] [Related]
19. Accumulation of "small dense" low density lipoproteins (LDL) in a homozygous patients with familial defective apolipoprotein B-100 results from heterogenous interaction of LDL subfractions with the LDL receptor. März W; Baumstark MW; Scharnagl H; Ruzicka V; Buxbaum S; Herwig J; Pohl T; Russ A; Schaaf L; Berg A J Clin Invest; 1993 Dec; 92(6):2922-33. PubMed ID: 8254047 [TBL] [Abstract][Full Text] [Related]
20. Activity of thrombocytes as a marker of sufficient intensity of LDL-apheresis in familial hypercholesterolaemia. Blaha M; Pecka M; Urbankova J; Blaha V; Maly J; Zadak Z; Blazek M Transfus Apher Sci; 2004 Apr; 30(2):83-7. PubMed ID: 15062743 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]