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[null,"1.","Record Nr.",null,"UNINA9910787592803321"]
[null,null,"Titolo",null,"Polycystic kidney disease : from bench to bedside / / editors, Vincent H. Gattone, Robert L. Bacall"]
[null,null,"Pubbl/distr/stampa",null,"London, England : , : Future Medicine Ltd., , [2013]"]
[{"$nulls":4},"©2013"]
[null,null,"ISBN",null,"1-78084-174-4"]
[null,null,"Edizione",null,"[1st ed.]"]
[null,null,"Descrizione fisica",null,"1 online resource (195 p.)"]
[null,null,"Disciplina",null,"616.61042"]
[null,null,"Soggetti",null,"Polycystic kidney disease"]
[{"$nulls":4},"Polycystic kidney disease - Diagnosis"]
[{"$nulls":4},"Polycystic kidney disease - Treatment"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,"Nota di contenuto",null,"Title page; Copyright page; Contents; Foreword. Polycystic kidney disease: from bench to bedside; 1. Polycystic kidney disease: genes, prevalence and diagnosis; 2. Polycystins and the pathophysiology of autosomal dominant polycystic kidney disease; 3. Fibrocystin/polyductin and pathophysiology of autosomal recessive polycystic kidney disease; 4. Nephronophthisis; 5. Meckel syndrome; 6. The Bardet-Biedl and orofacial digital type I ciliopathies; 7. Pain and pain management in polycystic kidney disease; 8. Hypertension in autosomal dominant polycystic kidney disease"]
[{"$nulls":4},"9. Complications of polycystic kidney disease10. End-stage renal disease in polycystic kidney disease; 11. Preclinical and clinical trials for identifying treatments for polycystic kidney disease; Index"]
[null,null,null,"Sommario/riassunto","Recent years have seen advances in our understanding the molecular cell biology, signaling and pathogenesis of one of the most common life-threatening genetic diseases - polycystic kidney disease (PKD). This multichapter work from international experts opens with chapters exploring the pathogenesis and pathophysiology of autosomal dominant and autosomal recessive PKD."]