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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 Autosomal dominant polycystic kidney disease: the changing face of clinical management
by Ong, Albert C M, Prof and Devuyst, Olivier, Prof and Knebelmann, Bertrand, Prof and Walz, Gerd, Prof and ERA-EDTA Working Group for Inherited Kidney Diseases and ERA-EDTA Working Grp Inherited Kid
The Lancet (British edition), ISSN 0140-6736, 2015, Volume 385, Issue 9981, pp. 1993 - 2002
Internal Medicine | Genetic Testing | Prognosis | Signal Transduction | Humans | Middle Aged | Protein-Serine-Threonine Kinases | Cyclic AMP | Male | Forecasting | Young Adult | Adolescent | TRPP Cation Channels | Adult | Female | Aged | TOR Serine-Threonine Kinases | Mutation | Child | Polycystic Kidney, Autosomal Dominant | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | TOR Serine-Threonine Kinases - metabolism | Polycystic Kidney, Autosomal Dominant - therapy | Protein-Serine-Threonine Kinases - genetics | Mutation - genetics | TRPP Cation Channels - genetics | Polycystic Kidney, Autosomal Dominant - diagnosis | Polycystic Kidney, Autosomal Dominant - etiology | Signal Transduction - physiology | Cyclic AMP - metabolism | Medical colleges | Development and progression | Polycystic kidney disease | Studies | Kidney diseases | Disease management | Epidemiology | Patients | Index Medicus | Abridged Index Medicus
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5. Full Text Autosomal Dominant Polycystic Kidney Disease
by Grantham, Jared J
The New England journal of medicine, ISSN 0028-4793, 10/2008, Volume 359, Issue 14, pp. 1477 - 1485
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 | Causes of | Care and treatment | Diagnosis | Polycystic kidney disease | Cysts | Mutation | Kidney diseases
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6. Autosomal dominant polycystic kidney disease
by Simms, Roslyn J
BMJ (Online), ISSN 0959-8146, 02/2016, Volume 352, p. i679
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Polycystic Kidney, Autosomal Dominant - genetics | Benzazepines - therapeutic use | Polycystic Kidney, Autosomal Dominant - diagnosis | Humans | Risk Factors | Hypertension - drug therapy | Disease Progression | Polycystic Kidney, Autosomal Dominant - complications | Polycystic Kidney, Autosomal Dominant - drug therapy | Antidiuretic Hormone Receptor Antagonists - therapeutic use | Hypertension - etiology
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7. Full Text Health-Related Quality of Life in Patients With Autosomal Dominant Polycystic Kidney Disease and CKD Stages 1-4: A Cross-sectional Study
by Miskulin, Dana C., MD and Abebe, Kaleab Z., PhD and Chapman, Arlene B., MD and Perrone, Ronald D., MD and Steinman, Theodore I., MD and Torres, Vicente E., MD and Bae, K. Ty, MD and Braun, William, MD and Winklhofer, Franz T., MD and Hogan, Marie C., MD and Rahbari-Oskoui, Fred, MD and Moore, Charity G., PhD and Flessner, Michael F., MD and Schrier, Robert W., MD and HALT-PKD Study
American journal of kidney diseases, ISSN 0272-6386, 2014, Volume 63, Issue 2, pp. 214 - 226
Nephrology | quality of life (QoL) | patient-reported outcomes | activities of daily life | extrarenal symptoms | Autosomal dominant polycystic kidney disease (ADPKD) | chronic kidney disease (CKD) | renal disease | Life Sciences & Biomedicine | Urology & Nephrology |