Polycystic Kidney Disease
Seiten
1996
Oxford University Press (Verlag)
978-0-19-262578-6 (ISBN)
Oxford University Press (Verlag)
978-0-19-262578-6 (ISBN)
Autosomal dominant polycystic kidney disease is thought to be the commonest disorder inherited autosomally. This book provides a review of the genetics, pathophysiology, evaluation, and management of autosomal diseases, and is of interest to both basic researchers and clinicians in nephrology.
Many inherited diseases and non-hereditary disorders have in common the development of renal cystic 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 R 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.
Many inherited diseases and non-hereditary disorders have in common the development of renal cystic 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 R 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.
COMPLEX
| Erscheint lt. Verlag | 21.3.1996 |
|---|---|
| Reihe/Serie | Oxford Clinical Nephrology Series |
| Zusatzinfo | halftones, line figures, tables |
| Verlagsort | Oxford |
| Sprache | englisch |
| Maße | 174 x 248 mm |
| Gewicht | 1293 g |
| Themenwelt | Medizinische Fachgebiete ► Innere Medizin ► Nephrologie |
| Studium ► 2. Studienabschnitt (Klinik) ► Anamnese / Körperliche Untersuchung | |
| Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
| ISBN-10 | 0-19-262578-0 / 0192625780 |
| ISBN-13 | 978-0-19-262578-6 / 9780192625786 |
| Zustand | Neuware |
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