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1. Full Text Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management—A KDIGO consensus report
by Eckardt, Kai-Uwe and Alper, Seth L and Antignac, Corinne and Bleyer, Anthony J and Chauveau, Dominique and Dahan, Karin and Deltas, Constantinos and Hosking, Andrew and Kmoch, Stanislav and Rampoldi, Luca and Wiesener, Michael and Wolf, Matthias T and Devuyst, Olivier and Kidney Disease: Improving Global Outcomes
Kidney international, ISSN 0085-2538, 10/2015, Volume 88, Issue 4, pp. 676 - 683
kidney disease | uromodulin | hepatocyte nuclear factor-1β | genetics | mucin-1 | renin | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Predictive Value of Tests | Humans | Kidney Diseases - diagnosis | Polycystic Kidney, Autosomal Dominant - therapy | Gout - diagnosis | Nephrology - standards | Kidney Diseases - genetics | Uromodulin - classification | Uromodulin - deficiency | Polycystic Kidney, Autosomal Dominant - genetics | DNA Mutational Analysis | Hyperuricemia - therapy | Uromodulin - genetics | Genetic Predisposition to Disease | Kidney Diseases - classification | Hyperuricemia - diagnosis | Hyperuricemia - classification | Terminology as Topic | Treatment Outcome | Consensus | Hyperuricemia - genetics | Gout - therapy | Phenotype | Polycystic Kidney, Autosomal Dominant - diagnosis | Kidney Diseases - therapy | Gout - classification | Gout - genetics | Polycystic Kidney, Autosomal Dominant - classification | Mutation | Index Medicus
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2. Full Text Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
by Chapman, Arlene B and Devuyst, Olivier and Eckardt, Kai-Uwe and Gansevoort, Ron T and Harris, Tess and Horie, Shigeo and Kasiske, Bertram L and Odland, Dwight and Pei, York and Perrone, Ronald D and Pirson, Yves and Schrier, Robert W and Torra, Roser and Torres, Vicente E and Watnick, Terry and Wheeler, David C and Conference Participants
Kidney international, ISSN 0085-2538, 07/2015, Volume 88, Issue 1, pp. 17 - 27
diagnosis | ADPKD | patient support | end-stage renal disease | management | polycystic kidney disease | FOLLOW-UP | INDIVIDUAL PATIENT DATA | LIVER-DISEASE | PREIMPLANTATION GENETIC DIAGNOSIS | UNRUPTURED INTRACRANIAL ANEURYSMS | CYST INFECTION | LONG-ACTING SOMATOSTATIN | LEFT-VENTRICULAR MASS | QUALITY-OF-LIFE | RENAL REPLACEMENT THERAPY | End-stage renal disease | Diagnosis | Management | Patient support | Polycystic kidney disease | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Index Medicus
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3. Full Text Autosomal dominant polycystic kidney disease
by Cornec-Le Gall, Emilie and Alam, Ahsan and Perrone, Ronald D
The Lancet (British edition), ISSN 0140-6736, 03/2019, Volume 393, Issue 10174, pp. 919 - 935
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Genetic Testing | Humans | Middle Aged | Polycystic Kidney, Autosomal Dominant - therapy | Male | Disease Progression | Cysts - complications | Randomized Controlled Trials as Topic | Magnetic Resonance Imaging | Polycystic Kidney, Autosomal Dominant - diagnosis | Ultrasonography | Liver Diseases - complications | Adult | Female | Aged | Polycystic Kidney, Autosomal Dominant - physiopathology | Mutation | Polycystic Kidney, Autosomal Dominant - complications | Hypertension | Medical colleges | Medical research | Chronic kidney failure | Molecular genetics | Liver | Medicine, Experimental | Aneurysms | Development and progression | Health aspects | Polycystic kidney disease | End-stage renal disease | Genomics | Genes | Clinical trials | Information systems | Proteins | Ultrasonic imaging | Genetics | Heart diseases | Enzymes | Kidneys | Liver diseases | Complications | Polycystic kidney | Health risks | Imaging techniques | Disease control | Patients | Coronary artery disease | Nutrition research | Cysts | Renal failure | Kidney diseases | Cardiovascular diseases | Endoplasmic reticulum | Index Medicus | Abridged Index Medicus
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4. Full Text Effect of longacting somatostatin analogue on kidney and cyst growth in autosomal dominant polycystic kidney disease (ALADIN): a randomised, placebo-controlled, multicentre trial
by Caroli, Anna, PhD and Perico, Norberto, MD and Perna, Annalisa, MSc and Antiga, Luca, PhD and Brambilla, Paolo, MD and Pisani, Antonio, MD and Visciano, Bianca, MD and Imbriaco, Massimo, MD and Messa, Piergiorgio, MD and Cerutti, Roberta, MD and Dugo, Mauro, MD and Cancian, Luca, MD and Buongiorno, Erasmo, MD and De Pascalis, Antonio, MD and Gaspari, Flavio, ChemD and Carrara, Fabiola, Chemist and Rubis, Nadia, Res Nurse and Prandini, Silvia, Res Nurse and Remuzzi, Andrea, EngD and Remuzzi, Giuseppe, Dr and Ruggenenti, Piero, MD and for the ALADIN study group and ALADIN Study Grp and ALADIN study group
The Lancet (British edition), ISSN 0140-6736, 2013, Volume 382, Issue 9903, pp. 1485 - 1495
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Tumors of the urinary system | General aspects | Kidneys | Nephrology. Urinary tract diseases | Biological and medical sciences | Medical sciences | Malformations of the urinary system | Somatostatin - analogs & derivatives | Kidney - drug effects | Follow-Up Studies | Kidney - pathology | Cholecystitis, Acute - chemically induced | Humans | Middle Aged | Polycystic Kidney, Autosomal Dominant - pathology | Octreotide - adverse effects | Male | Treatment Outcome | Octreotide - therapeutic use | Disease Progression | Magnetic Resonance Imaging | Organ Size - drug effects | Kidney Failure, Chronic - prevention & control | Gastrointestinal Agents - therapeutic use | Adult | Female | Italy | Gastrointestinal Agents - adverse effects | Cholelithiasis - chemically induced | Polycystic Kidney, Autosomal Dominant - drug therapy | Care and treatment | Octreotide acetate | Health aspects | Polycystic kidney disease | Proteins | Studies | Cell growth | Liver diseases | Cysts | Rodents | Kidney diseases | Urogenital system | Blood | Index Medicus | Abridged Index Medicus
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5. Full Text Tolvaptan in Patients with Autosomal Dominant Polycystic Kidney Disease
by Torres, Vicente E and Chapman, Arlene B and Devuyst, Olivier and Gansevoort, Ron T and Grantham, Jared J and Higashihara, Eiji and Perrone, Ronald D and Krasa, Holly B and Ouyang, John and Czerwiec, Frank S and TEMPO 3 4 Trial Investigators
The New England journal of medicine, ISSN 0028-4793, 12/2012, Volume 367, Issue 25, pp. 2407 - 2418
VOLUME PROGRESSION | VASOPRESSIN V-2-RECEPTOR ANTAGONIST | ORAL TOLVAPTAN | HYPONATREMIA | RENAL-FUNCTION | OPC-41061 | LONG-ACTING SOMATOSTATIN | V2 RECEPTOR ANTAGONIST | UMCG Approved | CYST GROWTH | SIROLIMUS | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Nephrology. Urinary tract diseases | Biological and medical sciences | General aspects | Kidneys | Medical sciences | Malformations of the urinary system | Drugs | Dose-response relationship (Biochemistry) | Product/Service Evaluations | Drug therapy | Polycystic kidney disease | Studies | Nuclear magnetic resonance--NMR | Kidney diseases | Cysts | Rodents | Index Medicus | Abridged Index Medicus
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6. Full Text Autosomal dominant polycystic kidney disease
by Torres, Vicente E, MD and Harris, Peter C, PhD and Pirson, Yves, MD
The Lancet (British edition), ISSN 0140-6736, 2007, Volume 369, Issue 9569, pp. 1287 - 1301
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Nephrology. Urinary tract diseases | Biological and medical sciences | General aspects | Kidneys | Medical sciences | Malformations of the urinary system | Cardiovascular Diseases - etiology | Humans | Kidney Tubules - physiology | Renal Replacement Therapy | Genotype | Male | Incidence | Kidney Failure, Chronic - therapy | Kidney Tubules - anatomy & histology | Animals | Kidney Failure, Chronic - epidemiology | Polycystic Kidney, Autosomal Dominant - genetics | Pain - etiology | Female | Polycystic Kidney, Autosomal Dominant - physiopathology | Kidney Tubules - metabolism | Polycystic Kidney, Autosomal Dominant - complications | Genetic aspects | Risk factors | Polycystic kidney disease | Medical research | Parents & parenting | Disease | Cysts | Rodents | African Americans | Kidney diseases | Mutation | Cells | Congenital diseases | Liver diseases | Polycystic kidney | Intellectual disabilities | Clinical trials | Kinases | Molecular chains | Proteins | Hernias | Localization | Endoplasmic reticulum | Age | Index Medicus | Abridged Index Medicus
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