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101 0 $aeng
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200 10$aAutosomal Dominant Polycystic Kidney Disease : $eSeminar, Vimercate, June 1994 / $f editors, A. Sessa, P. Serbelloni, S. Milani, F. Conte
210   $aBasel : $cS. Karger, $d1995
215   $a1 online resource (X + 192 pages) : $c  47 figures, 39 tables
225 0 $aContributions to Nephrology, $x1662-2782 ; $vVol.115
311   $a3-8055-6090-7 
330   $aThis volume contains over 40 informative contributions from leading specialists in the field focusing on the following inheritable diseases:  - Polycystic kidney disease  - Tuberous sclerosis complex  - Von Hippel-Lindau disease  - Alport syndrome  - Primary hyperoxaluria  - Cystinuria  - Anderson-Fabry disease   Recent scientific advances have changed our knowledge regarding several hereditary kidney diseases and the application of this knowledge will open a new era of molecular medicine in which the risk of disease can be accurately assessed by DNA-based diagnostic procedures. The appropriate use of preemptive medical care will benefit all patients and lower the social costs of certain diseases but ethical guidelines need to be clearly established. The goal of this volume is to bring together the latest findings of clinical nephrologists, geneticists and molecular biologists in order to further the clinical application of genetic diagnostic techniques for some of the most common inherited nephropathies. Throwing new light on a range of important topics and issues, the book is very valuable for all those interested in the field.
606   $aNephrology
606   $aGenetics
606   $aDialysis
606   $aMolecular Biology
606   $aPathology
606   $aUrology
615 14$aNephrology
615 14$aGenetics
615 24$aDialysis
615 24$aMolecular Biology
615 24$aPathology
615 24$aUrology
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996   $aAutosomal Dominant Polycystic Kidney Disease$92810372
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