Hypocomplementemic Type II Membranoproliferative Glomerulonephritis in a Male Patient with Familial Lecithin-Cholesterol Acyltransferase Deficiency due to Two Different Allelic Mutations-Reference-Cited by-同舟云学术

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Hypocomplementemic Type II Membranoproliferative Glomerulonephritis in a Male Patient with Familial Lecithin-Cholesterol Acyltransferase Deficiency due to Two Different Allelic Mutations

Published:2001 Issue:3 Volume:88 Page:268-272
ISSN:1660-8151
Container-title:Nephron
language:en
Short-container-title:Nephron

Author:

Sessa Adalberto,Battini Graziana,Meroni Mietta,Daidone Giuseppe,Carnera Ida,Brambilla Pier Luigi,Viganò Giovanni,Giordano Ferdinando,Pallotti Francesco,Torri Tarelli Laura,Calabresi Laura,Rolleri Marina,Bertolini Stefano

Publisher

S. Karger AG

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. HDL and chronic kidney disease;Atherosclerosis Plus;2023-06

2. A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency;Journal of Lipid Research;2022-03

3. LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred;Lipids in Health and Disease;2021-07-13

4. High-Density Lipoproteins and the Kidney;Cells;2021-03-31

5. Progression of chronic kidney disease in familial LCAT deficiency: a follow-up of the Italian cohort;Journal of Lipid Research;2020-12

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