This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Email citation

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 2007 Aug;27(8):1866-8.

doi: 10.1161/ATVBAHA.107.146639.

Prevalence of cholesteryl ester storage disease

Sandro Muntoni, Heiko Wiebusch, Marianne Jansen-Rust, Stephan Rust, Udo Seedorf, Helmut Schulte, Klaus Berger, Harald Funke, Gerd Assmann

PMID: 17634524
DOI: 10.1161/ATVBAHA.107.146639

Prevalence of cholesteryl ester storage disease

Sandro Muntoni et al. Arterioscler Thromb Vasc Biol. 2007 Aug.

. 2007 Aug;27(8):1866-8.

doi: 10.1161/ATVBAHA.107.146639.

Authors

Sandro Muntoni, Heiko Wiebusch, Marianne Jansen-Rust, Stephan Rust, Udo Seedorf, Helmut Schulte, Klaus Berger, Harald Funke, Gerd Assmann

PMID: 17634524
DOI: 10.1161/ATVBAHA.107.146639

No abstract available

PubMed Disclaimer

Similar articles

Cholesteryl ester storage disease. Report of a case.
Coelho CA, Balarin MA, Coelho KI. Coelho CA, et al. Arq Gastroenterol. 1987 Jul-Dec;24(3-4):184-7. Arq Gastroenterol. 1987. PMID: 3333127 Review.
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. Wiebusch H, et al. Clin Genet. 1996 Aug;50(2):106-7. Clin Genet. 1996. PMID: 8937772 No abstract available.
Estimation of the prevalence of cholesteryl ester storage disorder in a cohort of patients with clinical features of familial hypercholesterolaemia.
Ashfield-Watt P, Haralambos K, Edwards R, Townsend D, Gingell R, Wa Li K, Humphries SE, McDowell I. Ashfield-Watt P, et al. Ann Clin Biochem. 2019 Jan;56(1):112-117. doi: 10.1177/0004563218793165. Epub 2018 Aug 8. Ann Clin Biochem. 2019. PMID: 30056760
KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes.
Wichmann HE, Gieger C, Illig T; MONICA/KORA Study Group. Wichmann HE, et al. Gesundheitswesen. 2005 Aug;67 Suppl 1:S26-30. doi: 10.1055/s-2005-858226. Gesundheitswesen. 2005. PMID: 16032514 Review.
Screening for familial hypercholesterolemia: what is the most effective strategy?
Daniels SR. Daniels SR. Nat Clin Pract Cardiovasc Med. 2008 Mar;5(3):130-1. doi: 10.1038/ncpcardio1084. Epub 2007 Dec 4. Nat Clin Pract Cardiovasc Med. 2008. PMID: 18059381 No abstract available.

See all similar articles

Cited by

Frequency of rs1051338 and rs116928232 Variants in Individuals from Northwest Mexico.
Hernández-Orozco AA, Melendez-Aranda L, Mendoza-Ruvalcaba SDC, Perea-Díaz FJ, Cebolla JJ, Giraldo P, Brambila-Tapia AJL, García-Ortíz JE. Hernández-Orozco AA, et al. J Clin Lab Anal. 2024 Jul;38(13-14):e25083. doi: 10.1002/jcla.25083. Epub 2024 Aug 6. J Clin Lab Anal. 2024. PMID: 39105399 Free PMC article.
Lysosomal Acid Lipase Deficiency: Genetics, Screening, and Preclinical Study.
Mashima R, Takada S. Mashima R, et al. Int J Mol Sci. 2022 Dec 8;23(24):15549. doi: 10.3390/ijms232415549. Int J Mol Sci. 2022. PMID: 36555187 Free PMC article. Review.
Lysosomal acid lipase deficiency: A rare inherited dyslipidemia but potential ubiquitous factor in the development of atherosclerosis and fatty liver disease.
Besler KJ, Blanchard V, Francis GA. Besler KJ, et al. Front Genet. 2022 Sep 20;13:1013266. doi: 10.3389/fgene.2022.1013266. eCollection 2022. Front Genet. 2022. PMID: 36204319 Free PMC article. Review.
Early Discovery of Children With Lysosomal Acid Lipase Deficiency With the Universal Familial Hypercholesterolemia Screening Program.
Sustar U, Groselj U, Trebusak Podkrajsek K, Mlinaric M, Kovac J, Thaler M, Drole Torkar A, Skarlovnik A, Battelino T, Hovnik T. Sustar U, et al. Front Genet. 2022 Jul 12;13:936121. doi: 10.3389/fgene.2022.936121. eCollection 2022. Front Genet. 2022. PMID: 35903350 Free PMC article.
Living-Donor Liver Transplantation for Late-Onset Lysosomal Acid Lipase Deficiency.
Ramakrishna SH, Kasala MB, Perumal K, Malleeswaran S, Patcha RV, Varghese J. Ramakrishna SH, et al. J Clin Exp Hepatol. 2022 Mar-Apr;12(2):672-676. doi: 10.1016/j.jceh.2021.06.022. Epub 2021 Jul 6. J Clin Exp Hepatol. 2022. PMID: 35535100 Free PMC article.

See all "Cited by" articles

Publication types

Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Atypon
- Ovid Technologies, Inc.
Other Literature Sources
- The Lens - Patent Citations Database
Medical
- MedlinePlus Health Information