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13. Lipid compositions of plasma major lipoproteins and lipoprotein lipase activity in hypolipidemic and hyperlipidemic siblings with familial LCAT deficiency. Naito C; Teramoto T; Kato H; Watanabe T; Yamanaka T; Iwamoto A Scand J Clin Lab Invest Suppl; 1978; 150():168-76. PubMed ID: 746345 [No Abstract] [Full Text] [Related]
14. A new case of familial LCAT deficiency. Vergani C; Catapano AL; Roma P; Giudici G Acta Med Scand; 1983; 214(2):173-6. PubMed ID: 6624548 [TBL] [Abstract][Full Text] [Related]
16. Hereditary lecithin-cholesterol acyltransferase deficiency and Bloom syndrome in the same individual. Shojania AM; McAlpine PJ; Ray M Am J Med Genet; 1983 Mar; 14(3):479-85. PubMed ID: 6859101 [TBL] [Abstract][Full Text] [Related]
17. Genetic heterogeneity in familial lecithin:cholesterol acyltransferase (LCAT) deficiency. Teisberg P; Gjone E Acta Med Scand; 1981; 210(1-2):1-2. PubMed ID: 7027744 [No Abstract] [Full Text] [Related]
18. Spin label studies of erythrocytes with abnormal lipid composition: comparison of red cells in a hereditary hemolytic syndrome and lecithin: cholesterol acyltransferase deficiency. Godin DV; Herring FG J Supramol Struct Cell Biochem; 1981; 15(3):213-8. PubMed ID: 6267314 [TBL] [Abstract][Full Text] [Related]
19. [Both the enzymatic defect and the localization of the genetic defect has been clarified in the metabolic disease lecithin cholesterol acetyltransferase deficiency]. Hamnström B Lakartidningen; 1983 Jun; 80(24):2490-3. PubMed ID: 6888097 [No Abstract] [Full Text] [Related]
20. Hereditary lecithin-cholesterol acyltransferase deficiency. Report of 2 new cases and review of the literature. Shojania AM; Jain SK; Shohet SB Clin Invest Med; 1983; 6(1):49-55. PubMed ID: 6831794 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]