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- Gratis thuislevering in België vanaf € 30
- Ruim aanbod met 7 miljoen producten
€ 365,45
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Omschrijving
Many inherited diseases and non-herediatry disorders have in common the development of renal cyctic disease. The most common, autosonal dominant polycystic kidney disease, is responsible for 5-10% of end-stage renal failure treated by dialysis or transplantation.
Since the publication six years ago of the last book on polycystic kidney disease, a number of genes causing the disease have been identified, mapped, or sequenced; new experimental models and the application of molecular biology techniques have provided new insights into the pathogenesis of
polycystic kidney disease; novel clinical studies have provided valuable information for the prevention, evaluation, and treatment of the complications of this disease. This book provides an updated, state-of-the-art review of the genetics, pathophysiology, evaluation, and management of these
diseases and will be of interest to both basic researchers and clinicians in nephrology.
Since the publication six years ago of the last book on polycystic kidney disease, a number of genes causing the disease have been identified, mapped, or sequenced; new experimental models and the application of molecular biology techniques have provided new insights into the pathogenesis of
polycystic kidney disease; novel clinical studies have provided valuable information for the prevention, evaluation, and treatment of the complications of this disease. This book provides an updated, state-of-the-art review of the genetics, pathophysiology, evaluation, and management of these
diseases and will be of interest to both basic researchers and clinicians in nephrology.
Specificaties
Betrokkenen
- Auteur(s):
- Uitgeverij:
Inhoud
- Aantal bladzijden:
- 608
- Taal:
- Engels
- Reeks:
Eigenschappen
- Productcode (EAN):
- 9780192625786
- Verschijningsdatum:
- 1/07/1996
- Uitvoering:
- Hardcover
- Formaat:
- Genaaid
- Afmetingen:
- 224 mm x 249 mm
- Gewicht:
- 1256 g
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