These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
139 related articles for article (PubMed ID: 7751811)
21. A novel variant of lysosomal acid lipase in cholesteryl ester storage disease associated with mild phenotype and improvement on lovastatin. Gasche C; Aslanidis C; Kain R; Exner M; Helbich T; Dejaco C; Schmitz G; Ferenci P J Hepatol; 1997 Oct; 27(4):744-50. PubMed ID: 9365051 [TBL] [Abstract][Full Text] [Related]
22. Tissue and cellular specific expression of murine lysosomal acid lipase mRNA and protein. Du H; Witte DP; Grabowski GA J Lipid Res; 1996 May; 37(5):937-49. PubMed ID: 8725147 [TBL] [Abstract][Full Text] [Related]
23. Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene. Pisciotta L; Fresa R; Bellocchio A; Pino E; Guido V; Cantafora A; Di Rocco M; Calandra S; Bertolini S Mol Genet Metab; 2009 Jun; 97(2):143-8. PubMed ID: 19307143 [TBL] [Abstract][Full Text] [Related]
24. A novel missense LIPA gene mutation, N98S, in a patient with cholesteryl ester storage disease. Hooper AJ; Tran HA; Formby MR; Burnett JR Clin Chim Acta; 2008 Dec; 398(1-2):152-4. PubMed ID: 18775687 [TBL] [Abstract][Full Text] [Related]
25. Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase -1 exon 8 splice junction mutation. vom Dahl S; Harzer K; Rolfs A; Albrecht B; Niederau C; Vogt C; van Weely S; Aerts J; Müller G; Häussinger D J Hepatol; 1999 Oct; 31(4):741-6. PubMed ID: 10551400 [TBL] [Abstract][Full Text] [Related]
26. Crystal structure of human lysosomal acid lipase and its implications in cholesteryl ester storage disease. Rajamohan F; Reyes AR; Tu M; Nedoma NL; Hoth LR; Schwaid AG; Kurumbail RG; Ward J; Han S J Lipid Res; 2020 Aug; 61(8):1192-1202. PubMed ID: 32482718 [TBL] [Abstract][Full Text] [Related]
27. Lysosomal acid lipase deficiency: wolman disease and cholesteryl ester storage disease. Tylki-Szymańska A; Jurecka A Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2014; 35(1):99-106. PubMed ID: 24798600 [TBL] [Abstract][Full Text] [Related]
28. Exon 10 skipping caused by intron 10 splice donor site mutation in cholesteryl ester transfer protein gene results in abnormal downstream splice site selection. Sakai N; Santamarina-Fojo S; Yamashita S; Matsuzawa Y; Brewer HB J Lipid Res; 1996 Oct; 37(10):2065-73. PubMed ID: 8906584 [TBL] [Abstract][Full Text] [Related]
29. Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life span. Du H; Heur M; Duanmu M; Grabowski GA; Hui DY; Witte DP; Mishra J J Lipid Res; 2001 Apr; 42(4):489-500. PubMed ID: 11290820 [TBL] [Abstract][Full Text] [Related]
30. Occurrence of a mutation associated with Wolman disease in a family with cholesteryl ester storage disease. Maslen CL; Babcock D; Illingworth DR J Inherit Metab Dis; 1995; 18(5):620-3. PubMed ID: 8598644 [TBL] [Abstract][Full Text] [Related]
32. A rare cause of hepatomegaly and dyslipidemia: lysosomal acid lipase deficiency. Gürbüz BB; Güney İ; Bulut FD; Dilek O Turk J Pediatr; 2020; 62(5):831-835. PubMed ID: 33108087 [TBL] [Abstract][Full Text] [Related]
33. Enzyme therapy for lysosomal acid lipase deficiency in the mouse. Du H; Schiavi S; Levine M; Mishra J; Heur M; Grabowski GA Hum Mol Genet; 2001 Aug; 10(16):1639-48. PubMed ID: 11487567 [TBL] [Abstract][Full Text] [Related]
34. Frequency of the cholesteryl ester storage disease common LIPA E8SJM mutation (c.894G>A) in various racial and ethnic groups. Scott SA; Liu B; Nazarenko I; Martis S; Kozlitina J; Yang Y; Ramirez C; Kasai Y; Hyatt T; Peter I; Desnick RJ Hepatology; 2013 Sep; 58(3):958-65. PubMed ID: 23424026 [TBL] [Abstract][Full Text] [Related]
35. Purification, characterization and molecular cloning of human hepatic lysosomal acid lipase. Ameis D; Merkel M; Eckerskorn C; Greten H Eur J Biochem; 1994 Feb; 219(3):905-14. PubMed ID: 8112342 [TBL] [Abstract][Full Text] [Related]
36. A novel missense mutation (Gly2Arg) in the human lysosomal acid lipase gene is found in individuals with and without cholesterol ester storage disease (CESD). Wiebusch H; Muntoni S; Funke H; Lu F; Seedorf U; Oberle S; Schwarzer U; Assmann G Clin Genet; 1996 Aug; 50(2):106-7. PubMed ID: 8937772 [No Abstract] [Full Text] [Related]
37. Extended use of a selective inhibitor of acid lipase for the diagnosis of Wolman disease and cholesteryl ester storage disease. Civallero G; De Mari J; Bittar C; Burin M; Giugliani R Gene; 2014 Apr; 539(1):154-6. PubMed ID: 24508470 [TBL] [Abstract][Full Text] [Related]