Characteristic kidney pathology, gene abnormality and treatments in LCAT deficiency-Reference-Cited by-同舟云学术

Characteristic kidney pathology, gene abnormality and treatments in LCAT deficiency

Published:2013-10-31 Issue:2 Volume:18 Page:189-193
ISSN:1342-1751
Container-title:Clinical and Experimental Nephrology
language:en
Short-container-title:Clin Exp Nephrol

Author:

Hirashio Shuma,Ueno Toshinori,Naito Takayuki,Masaki Takao

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Nephrology,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s10157-013-0895-4.pdf

Reference28 articles.

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2. Gjone E. Familial lecithin:cholesterol acyltransferase deficiency—a new metabolic disease with renal involvement. Adv Nephrol Necker Hosp. 1981;10:167–85.

3. Reichl D, Miller NE. Pathophysiology of reverse cholesterol transport. Insights from inherited disorders of lipoprotein metabolism. Arteriosclerosis. 1989;9:785–97.

4. Tall AR. Plasma high density lipoproteins. Metabolism and relationship to atherogenesis. J Clin Invest. 1990;86:379–84.

5. Norum KR, Gjone E. Familial plasma lecithin: cholesterol acyltransferase deficiency. Scand J Clin Invest. 1967;20:231–43.

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