Lipoprotein glomerulopathy (LPG), a rare renal disease, is mainly reported in Japan and China. Chinese cases of LPG showed similar clinical and pathological features as reports from other countries. Three types of APOE mutation have been detected in those patients: APOE Maebashi (142Arg-144Leu-0) and APOE Kyoto (Arg25-Cys) were initially reported, and APOE Guangzhou (Arg150-Pro) is a novel mutation in Chinese patients with LPG. Asymptomatic carriers of all three mutations exist in families, but serum lipid and apolipoprotein E (apoE) levels are markedly elevated. In most of Chinese patients with LPG, long-term treatment with statins or bezafibrates appears to decrease proteinuria. LPG provides a disease model by which to explore pathogenic ...
Apolipoprotein E polymorphism and renal diseaseBackgroundLipid abnormalities are frequently found in...
AbstractThe purpose of the present study was to identify genetic variants that confer susceptibility...
This is an open access article published under the Creative Commons CC-BY-NC 3.0 license
Background: Lipoprotein glomerulopathy (LPG) is a unique disease characterized by thrombus-like lipo...
Background/Aims: Lipoprotein glomerulopathy (LPG) is a rare hereditary disease. In this study, we in...
Background: Lipoprotein glomerulopathy is a rare kidney disease characterized by lipoprotein thrombi...
Abstract Background Lipoprotein glomerulopathy (LPG) is a rare autosomal dominant disease caused by ...
A novel apolipoprotein E mutation, E2 (Arg25Cys), in lipoprotein glomerulopathy.BackgroundLipoprotei...
Abstract Lipoprotein glomerulopathy (LPG) is an uncommon cause of nephrotic syndrome and/or kidney f...
Abstract Background: Lipoprotein glomerulopathy (LPG) is a rare kidney disease, mainly reported in...
A novel 18-amino acid deletion in apolipoprotein E associated with lipoprotein glomerulopathy.Backgr...
Lipoprotein glomerulopathy is a pathological condition characterized by lipid accumulation in the gl...
Lipoprotein glomerulopathy (LPG) is a rare disease characterized by laminated lipid thrombi in the l...
Lipoprotein glomerulopathy is a pathological condition characterized by lipid accumulation in the gl...
We report on a 12-year-old female patient with lipoprotein glomerulopathy (LPG) who was proven to be...
Apolipoprotein E polymorphism and renal diseaseBackgroundLipid abnormalities are frequently found in...
AbstractThe purpose of the present study was to identify genetic variants that confer susceptibility...
This is an open access article published under the Creative Commons CC-BY-NC 3.0 license
Background: Lipoprotein glomerulopathy (LPG) is a unique disease characterized by thrombus-like lipo...
Background/Aims: Lipoprotein glomerulopathy (LPG) is a rare hereditary disease. In this study, we in...
Background: Lipoprotein glomerulopathy is a rare kidney disease characterized by lipoprotein thrombi...
Abstract Background Lipoprotein glomerulopathy (LPG) is a rare autosomal dominant disease caused by ...
A novel apolipoprotein E mutation, E2 (Arg25Cys), in lipoprotein glomerulopathy.BackgroundLipoprotei...
Abstract Lipoprotein glomerulopathy (LPG) is an uncommon cause of nephrotic syndrome and/or kidney f...
Abstract Background: Lipoprotein glomerulopathy (LPG) is a rare kidney disease, mainly reported in...
A novel 18-amino acid deletion in apolipoprotein E associated with lipoprotein glomerulopathy.Backgr...
Lipoprotein glomerulopathy is a pathological condition characterized by lipid accumulation in the gl...
Lipoprotein glomerulopathy (LPG) is a rare disease characterized by laminated lipid thrombi in the l...
Lipoprotein glomerulopathy is a pathological condition characterized by lipid accumulation in the gl...
We report on a 12-year-old female patient with lipoprotein glomerulopathy (LPG) who was proven to be...
Apolipoprotein E polymorphism and renal diseaseBackgroundLipid abnormalities are frequently found in...
AbstractThe purpose of the present study was to identify genetic variants that confer susceptibility...
This is an open access article published under the Creative Commons CC-BY-NC 3.0 license