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Proteinuria[electronic resource] :basic mechanisms, pathophysiology and clinical relevance /

紀錄類型:	書目-電子資源 : Monograph/item
杜威分類號:	616.63
書名/作者:	Proteinuria : basic mechanisms, pathophysiology and clinical relevance // edited by Judith Blaine.
其他作者:	Blaine, Judith.
出版者:	Cham : : Springer International Publishing :, 2016.
面頁冊數:	vii, 145 p. : : ill., digital ;; 24 cm.
Contained By:	Springer eBooks
標題:	Proteinuria.
標題:	Life Sciences.
標題:	Protein Science.
標題:	Protein Structure.
標題:	Nephrology.
標題:	Human Physiology.
標題:	Atomic/Molecular Structure and Spectra.
標題:	Molecular Medicine.
ISBN:	9783319433592
ISBN:	9783319433578
內容註:	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.
摘要、提要註:	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.
電子資源:	http://dx.doi.org/10.1007/978-3-319-43359-2

Proteinuria[electronic resource] :basic mechanisms, pathophysiology and clinical relevance /
Proteinuriabasic mechanisms, pathophysiology and clinical relevance /[electronic resource] :edited by Judith Blaine. - Cham :Springer International Publishing :2016. - vii, 145 p. :ill., digital ;24 cm.

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:

672577
Proteinuria.

LC Class. No.: RC905

Dewey Class. No.: 616.63

Proteinuria[electronic resource] :basic mechanisms, pathophysiology and clinical relevance /
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