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Proteinuria: Basic Mechanisms, Patho...
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Proteinuria: Basic Mechanisms, Pathophysiology and Clinical Relevance
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Proteinuria: Basic Mechanisms, Pathophysiology and Clinical Relevance/ edited by Judith Blaine.
other author:
Blaine, Judith.
Description:
VII, 145 p. 11 illus., 10 illus. in color.online resource. :
Contained By:
Springer Nature eBook
Subject:
Proteins . -
Online resource:
https://doi.org/10.1007/978-3-319-43359-2
ISBN:
9783319433592
Proteinuria: Basic Mechanisms, Pathophysiology and Clinical Relevance
Proteinuria: Basic Mechanisms, Pathophysiology and Clinical Relevance
[electronic resource] /edited by Judith Blaine. - 1st ed. 2016. - VII, 145 p. 11 illus., 10 illus. in color.online resource.
1. Evaluation and Epidemiology of Proteinuria -- 2. Glomerular Mechanisms of Proteinuria -- 3. Tubular Mechanisms of Proteinuria -- 4. Pathophysiology of Diabetic Nephropathy -- 5. Immune-Mediated Mechanisms of Proteinuria -- 6. Minimal Change Disease -- 7. Focal segmental glomerulosclerosis and its pathophysiology.
Recent work has begun to elucidate at the molecular level how albumin is handled by the kidney and how albuminuria develops in various proteinuric diseases including minimal change disease and focal segmental glomerulosclerosis. This volume provides a comprehensive overview of the renal handling of albumin – from basic mechanisms to the pathophysiology of proteinuric diseases. In describing the basic mechanisms of albuminuria, a particular highlight will be the focus on advanced imaging techniques such as intravital microscopy that have allowed a detailed “window” into albumin transit through the kidney. The volume will cover the epidemiological studies which show that albuminuria is a strong and independent marker of kidney disease progression and cardiovascular events, the molecular details of albumin handling in the kidney at the level of the glomerulus and the proximal tubule and the pathophysiology of proteinuric diseases including minimal change disease, membranous nephropathy, focal segmental glomerulosclerosis and diabetic nephropathy.
ISBN: 9783319433592
Standard No.: 10.1007/978-3-319-43359-2doiSubjects--Topical Terms:
1253493
Proteins .
LC Class. No.: QD431-431.7
Dewey Class. No.: 572.6
Proteinuria: Basic Mechanisms, Pathophysiology and Clinical Relevance
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1. Evaluation and Epidemiology of Proteinuria -- 2. Glomerular Mechanisms of Proteinuria -- 3. Tubular Mechanisms of Proteinuria -- 4. Pathophysiology of Diabetic Nephropathy -- 5. Immune-Mediated Mechanisms of Proteinuria -- 6. Minimal Change Disease -- 7. Focal segmental glomerulosclerosis and its pathophysiology.
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Recent work has begun to elucidate at the molecular level how albumin is handled by the kidney and how albuminuria develops in various proteinuric diseases including minimal change disease and focal segmental glomerulosclerosis. This volume provides a comprehensive overview of the renal handling of albumin – from basic mechanisms to the pathophysiology of proteinuric diseases. In describing the basic mechanisms of albuminuria, a particular highlight will be the focus on advanced imaging techniques such as intravital microscopy that have allowed a detailed “window” into albumin transit through the kidney. The volume will cover the epidemiological studies which show that albuminuria is a strong and independent marker of kidney disease progression and cardiovascular events, the molecular details of albumin handling in the kidney at the level of the glomerulus and the proximal tubule and the pathophysiology of proteinuric diseases including minimal change disease, membranous nephropathy, focal segmental glomerulosclerosis and diabetic nephropathy.
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