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Proteinuria: Basic Mechanisms, Pathophysiology and Clinical Relevance

  • Judith Blaine

Table of contents

  1. Front Matter
    Pages i-vii
  2. Evgenia Dobrinskikh, Judith Blaine
    Pages 11-21
  3. Sudhanshu K. Verma, Bruce A. Molitoris
    Pages 23-40
  4. Michal Herman-Edelstein, Sonia Q. Doi
    Pages 41-65
  5. Lindsey Goetz, Joshua M. Thurman
    Pages 67-84
  6. Gabriel M. Cara-Fuentes, Richard J. Johnson, Eduardo H. Garin
    Pages 85-116
  7. James Dylewski, Judith Blaine
    Pages 117-139
  8. Back Matter
    Pages 141-145

About this book

Introduction

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.

Keywords

Proteinuria diabetic nephropathy kidney disease membranous nephropathy podocyte biology

Editors and affiliations

  • Judith Blaine
    • 1
  1. 1.Division of Renal Diseases and HypertensionUniversity of Colorado DenverAuroraUSA

Bibliographic information

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