A Paediatric Clinical Phenotype Variant of Lysosomal Acid Lipase Deficiency Responsive to an HMG CoA Reductase Inhibitor (Simvastatin) plus Cholestyramine-Reference-Cited by-同舟云学术

A Paediatric Clinical Phenotype Variant of Lysosomal Acid Lipase Deficiency Responsive to an HMG CoA Reductase Inhibitor (Simvastatin) plus Cholestyramine

Published:1993-01 Issue:1 Volume:5 Page:35-38
ISSN:0114-2402
Container-title:Drug Investigation
language:en
Short-container-title:Drug Invest

Author:

Leone Luciano,Antonicelli Roberto,Giunta Sergio,Paciaroni Enrico,Ippoliti Paolo F.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),General Medicine,Pharmacology (medical)

Link

http://link.springer.com/content/pdf/10.1007/BF03259224.pdf

Reference14 articles.

1. Bretagne MC, Riovoal JE, Beley G, et al. La maladie de Wolman, cause rare de calcificantions surrenaliennes chez le nourrisson. Une observation. Journal de Radiologie 62: 197, 1981

2. Burton BK, Reed SP. Acid lipase cross-reacting material in Wolman disease and cholesteryl ester storage disease. American Journal of Human Genetics 33: 203–208, 1981

3. Di Bisceglie AM, Ishak KG, Rabin L, et al. Cholesteryl ester storage disease: hepatopathology and effects of therapy with lovastatin. Hepatology 11: 746–772, 1990

4. Ginsberg HN, Le NA, Short MP, et al. Suppression of apolipo-protein B production during treatment of cholesteryl ester storage disease with lovastatin. Journal of Clinical Investigation 80: 1692–1697, 1987

5. Hoeg JM, Demosky SJ, Pescovitz OH, et al. Cholesteryl ester storage disease and Wolman disease: phenotypic variants of lysosomal acid cholesteryl ester hydrolase deficiency. American Journal of Human Genetics 36: 1190–1203, 1984

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