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43. Possible induction of renal dysfunction in patients with lecithin:cholesterol acyltransferase deficiency by oxidized phosphatidylcholine in glomeruli. Jimi S; Uesugi N; Saku K; Itabe H; Zhang B; Arakawa K; Takebayashi S Arterioscler Thromb Vasc Biol; 1999 Mar; 19(3):794-801. PubMed ID: 10073988 [TBL] [Abstract][Full Text] [Related]
44. Amelioration of circulating lipoprotein profile and proteinuria in a patient with LCAT deficiency due to a novel mutation (Cys74Tyr) in the lid region of LCAT under a fat-restricted diet and ARB treatment. Naito S; Kamata M; Furuya M; Hayashi M; Kuroda M; Bujo H; Kamata K Atherosclerosis; 2013 May; 228(1):193-7. PubMed ID: 23522979 [TBL] [Abstract][Full Text] [Related]
45. The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families. Skretting G; Blomhoff JP; Solheim J; Prydz H FEBS Lett; 1992 Sep; 309(3):307-10. PubMed ID: 1516702 [TBL] [Abstract][Full Text] [Related]
46. [LCAT deficiency: a nephrological diagnosis]. Boscutti G; Calabresi L; Pizzolitto S; Boer E; Bosco M; Mattei PL; Martone M; Milutinovic N; Berbecar D; Beltram E; Franceschini G G Ital Nefrol; 2011; 28(4):369-82. PubMed ID: 21809306 [TBL] [Abstract][Full Text] [Related]
47. High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations. Holleboom AG; Kuivenhoven JA; Peelman F; Schimmel AW; Peter J; Defesche JC; Kastelein JJ; Hovingh GK; Stroes ES; Motazacker MM Hum Mutat; 2011 Nov; 32(11):1290-8. PubMed ID: 21901787 [TBL] [Abstract][Full Text] [Related]
48. A novel LCAT mutation (Phe382-->Val) in a kindred with familial LCAT deficiency and defective apolipoprotein B-100. Nanjee MN; Stocks J; Cooke CJ; Molhuizen HO; Marcovina S; Crook D; Kastelein JP; Miller NE Atherosclerosis; 2003 Sep; 170(1):105-13. PubMed ID: 12957688 [TBL] [Abstract][Full Text] [Related]
49. A review on lecithin:cholesterol acyltransferase deficiency. Saeedi R; Li M; Frohlich J Clin Biochem; 2015 May; 48(7-8):472-5. PubMed ID: 25172171 [TBL] [Abstract][Full Text] [Related]
50. A new case of familial lecithin: cholesterol acyltransferase (LCAT) deficiency--paradoxical findings regarding LCAT mass and activity in 23 members of a family. Takata K; Kajiyama G; Horiuchi I; Watanabe T; Tokumo H; Hirata Y Jpn J Med; 1989; 28(6):765-71. PubMed ID: 2634146 [TBL] [Abstract][Full Text] [Related]
53. 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]
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60. A first British case of fish-eye disease presenting at age 75 years: a double heterozygote for defined and new mutations affecting LCAT structure and expression. Winder AF; Owen JS; Pritchard PH; Lloyd-Jones D; Vallance DT; White P; Wray R J Clin Pathol; 1999 Mar; 52(3):228-30. PubMed ID: 10450185 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]