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by Kar-neng Lai

Download Recent Advances in IgA Nephropathy fb2, epub

ISBN: 9812835865
Author: Kar-neng Lai
Language: English
Publisher: World Scientific Pub Co Inc; 1 edition (January 14, 2009)
Pages: 419
Category: Medicine
Subcategory: Medicine
Rating: 4.4
Votes: 315
Size Fb2: 1949 kb
Size ePub: 1353 kb
Size Djvu: 1187 kb
Other formats: azw docx lrf azw


IgA nephropathy is the most common primary glomerulonephritis in developed countries. The primary defect lies in the abnormalities of the IgA molecule. The disease affects all ages, mainly in the young adults, and may recur in a transplanted kidney

IgA nephropathy is the most common primary glomerulonephritis in developed countries. The disease affects all ages, mainly in the young adults, and may recur in a transplanted kidney. This outstanding volume provides a comprehensive overview of the advances in this disease over the last ten years. It covers the genetics, epidemiology, clinicopathological features, pathogenesis, prognostic mechanisms, and treatment of this unique disease

Personal Name: Lai, Kar Neng.

Personal Name: Lai, Kar Neng. Download DOC book format.

IgA nephropathy, identified 50 years ago in France, is the most frequent glomerular disease worldwide. The course is variable, but in most of the cases there is a relentless decline in renal function, reaching end-stage renal failure in 10-60% of the cases after 10 years and in 40% after 20 years. These data justify the interest for finding a suitable therapeutic approach particularly in progressive cases. A supportive care, including renin-angiotensin system inhibitors is the priority in cases with slowly declining renal function, particularly when developing proteinuria.

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Kar Neng Lai. IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide and remains an. .Recently, a series of important advances in the area of communication between the glomerular mesangium and renal tubular cells have emerged. IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide and remains an important cause of end-stage renal failure. However, the basic molecular mechanism(s) underlying abnormal IgA synthesis, selective mesangial deposition with ensuing mesangial cell proliferation and extracellular matrix expansion remains poorly understood. These novel findings regarding the molecular pathogenesis of IgAN will be helpful in designing future directions for therapy.

IgA nephropathy is the most common primary glomerulonephritis in.You are leaving VitalSource and being redirected to Recent Advances In Iga Nephropathy. eTextbook Return Policy.

IgA nephropathy is the most common primary glomerulonephritis in developed countries. The book covers all clinical, pathological and molecular aspects of IgA nephropathy. This is an essential source of reference for nephrologists, internists, pathologists, and molecular biologists. The world’s eTextbook reader for students.

IgA nephropathy (IgAN) is characterized by mesangial deposition of pathogenic polymeric IgA1 with rare deposits in the tubular epithelial cells (TEC). Cochlear and Brainstem Implants, Volume 72, pp 40-44; doi:10. It covers the genetics, epidemiology, clinicopathological features, pathogenesis, prognostic mechanisms, and treatment of this unique disease

BACKGROUND Sera of IgA nephropathy (IgAN) patients contain high levels of circulating immune complexes composed of.Recent Advances in IgA Nephropathy. Noninvasive biomarkers in IgA nephropathy. Ewelina Olczyk, Magdalena Krajewska.

Recent Advances in IgA Nephropathy.

Kar Neng Lai Joseph C K Leung Sydney C W Tang. Epub 2016 Feb 11. Nephrology Division Department of Medicine, University of Hong Kong, Queen Mary Hospital, Hong Kong. Since its first description in 1968, IgA nephropathy has remained the most common form of primary glomerulonephritis leading to chronic kidney disease in developed countries. The clinical progression varies, and consequent end-stage renal disease occurs in 30% to 40% of patients 20 to 30 years after the first clinical presentation.

IgA nephropathy is the most common primary glomerulonephritis in developed countries. The primary defect lies in the abnormalities of the IgA molecule. The disease affects all ages, mainly in the young adults, and may recur in a transplanted kidney.This outstanding volume provides a comprehensive overview of the advances in this disease over the last ten years. It covers the genetics, epidemiology, clinicopathological features, pathogenesis, prognostic mechanisms, and treatment of this unique disease. Twenty-seven chapters are written by 43 experts from 13 countries; these experts have been providing forefront scientific findings to the scientific community for the last 20 years. The book covers all clinical, pathological and molecular aspects of IgA nephropathy. This is an essential source of reference for nephrologists, internists, pathologists, and molecular biologists. It is also suitable reading for graduate students or research scientists in the field of kidney diseases.

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