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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
Rare autosomal dominant tubulointerstitial kidney disease is caused by mutations in the genes encoding uromodulin (UMOD), hepatocyte nuclear factor-1 beta... 
kidney disease | uromodulin | hepatocyte nuclear factor-1β | genetics | mucin-1 | renin | UMOD GENE | TAMM-HORSFALL PROTEIN | RENAL-DISEASE | JUVENILE HYPERURICEMIC NEPHROPATHY | HEPATOCYTE NUCLEAR FACTOR-1-BETA | HYPERTENSIVE PATIENTS | CELL CARCINOMA | SERUM URIC-ACID | MEDULLARY CYSTIC-DISEASE | UROLOGY & NEPHROLOGY | hepatocyte nuclear factor-1 beta | 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
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2. Full Text Imaging-based diagnosis of autosomal dominant polycystic kidney disease
by Pei, York and Hwang, Young-Hwan and Conklin, John and Sundsbak, Jamie L and Heyer, Christina M and Chan, Winnie and Wang, Kairong and He, Ning and Rattansingh, Anand and Atri, Mostafa and Harris, Peter C and Haider, Masoom A
Journal of the American Society of Nephrology, ISSN 1046-6673, 03/2015, Volume 26, Issue 3, pp. 746 - 753
The clinical use of conventional ultrasonography (US) in autosomal dominant polycystic kidney disease (ADPKD) is currently limited by reduced diagnostic... 
CRITERIA | MUTATED GENE | ADPKD | CYSTS | UROLOGY & NEPHROLOGY | RENAL-DISEASE | PREVALENCE | PKD1 | SEVERITY | Young Adult | Magnetic Resonance Imaging | Polycystic Kidney, Autosomal Dominant - diagnostic imaging | Humans | Adolescent | Ultrasonography | Adult | Female | Male | Case-Control Studies | autosomal dominant polycystic kidney disease | Clinical Research | polycystic kidney disease | clinical epidemiology
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3. Full Text P04.03: In utero diagnosis of autosomal dominant polycystic kidney disease
by Cal, M and Godinho, I and Soeiro e Sá, M and Cunha, M and Carvalho, R
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 10/2019, Volume 54, Issue S1, pp. 165 - 165
Polycystic kidney | Kidney diseases
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4. 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
Autosomal-dominant polycystic kidney disease (ADPKD) affects up to 12 million individuals and is the fourth most common cause for renal replacement therapy... 
diagnosis | ADPKD | patient support | end-stage renal disease | management | polycystic kidney disease | End-stage renal disease | Diagnosis | Management | Patient support | Polycystic kidney disease | FOLLOW-UP | LIVER-DISEASE | NATIVE NEPHRECTOMY | PREIMPLANTATION GENETIC DIAGNOSIS | UNRUPTURED INTRACRANIAL ANEURYSMS | UROLOGY & NEPHROLOGY | CYST INFECTION | LONG-ACTING SOMATOSTATIN | LEFT-VENTRICULAR MASS | QUALITY-OF-LIFE | RENAL REPLACEMENT THERAPY | Humans | Polycystic Kidney, Autosomal Dominant - therapy | Consensus | Disease Progression | Kidney Failure, Chronic - therapy | Kidney Failure, Chronic - prevention & control | Polycystic Kidney, Autosomal Dominant - diagnosis | Hypertension - complications | Polycystic Kidney, Autosomal Dominant - physiopathology | Hypertension - therapy | Hypertension - diagnosis | Polycystic Kidney, Autosomal Dominant - complications | Kidney Failure, Chronic - etiology
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5. 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 Grp Inherited Kid and ERA-EDTA Working Group for Inherited Kidney Diseases
The Lancet, ISSN 0140-6736, 2015, Volume 385, Issue 9981, pp. 1993 - 2002
Summary Autosomal dominant polycystic kidney disease is the most common inherited kidney disease and accounts for 7–10% of all patients on renal replacement... 
Internal Medicine | MEDICINE, GENERAL & INTERNAL | ADPKD | GENE | VOLUME | RENAL-FUNCTION | RECEPTOR | LEFT-VENTRICULAR MASS | MUTATIONS | CYST GROWTH | PROGRESSION | PRIMARY CILIA | Genetic Testing | Prognosis | TOR Serine-Threonine Kinases - metabolism | Humans | Middle Aged | Polycystic Kidney, Autosomal Dominant - therapy | Protein-Serine-Threonine Kinases - genetics | Male | Mutation - genetics | Forecasting | TRPP Cation Channels - genetics | Young Adult | Polycystic Kidney, Autosomal Dominant - diagnosis | Adolescent | Polycystic Kidney, Autosomal Dominant - etiology | Adult | Female | Signal Transduction - physiology | Aged | Child | Cyclic AMP - metabolism | Medical colleges | Development and progression | Polycystic kidney disease | Studies | Kidney diseases | Disease management | Epidemiology | Patients
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6. Full Text Imaging classification of autosomal dominant polycystic kidney disease: A simple model for selecting patients for clinical trials
by Irazabal, María V and Rangel, Laureano J and Bergstralh, Eric J and Osborn, Sara L and Harmon, Amber J and Sundsbak, Jamie L and Bae, Kyongtae T and Chapman, Arlene B and Grantham, Jared J and Mrug, Michal and Hogan, Marie C and El-Zoghby, Ziad M and Harris, Peter C and Erickson, Bradley J and King, Bernard F and Torres, Vicente E and CRISP Investigators and the CRISP Investigators
Journal of the American Society of Nephrology, ISSN 1046-6673, 01/2015, Volume 26, Issue 1, pp. 160 - 172
The rate of renal disease progression varies widely among patients with autosomal dominant polycystic kidney disease (ADPKD), necessitating optimal patient... 
CONSORTIUM | ADPKD | DETERMINANTS | GROWTH | TOLVAPTAN | UROLOGY & NEPHROLOGY | LONG-ACTING SOMATOSTATIN | RENAL VOLUME | PROGRESSION | MOSAICISM | SIROLIMUS | Kidney Failure, Chronic - mortality | Glomerular Filtration Rate | Kidney Failure, Chronic - diagnosis | Age Factors | Kidney - pathology | Humans | Middle Aged | Polycystic Kidney, Autosomal Dominant - pathology | Male | Tomography, X-Ray Computed | Clinical Trials as Topic | Disease Progression | Patient Selection | Magnetic Resonance Imaging | Polycystic Kidney, Autosomal Dominant - mortality | Image Processing, Computer-Assisted | Kidney Failure, Chronic - pathology | Polycystic Kidney, Autosomal Dominant - diagnosis | Aged, 80 and over | Adult | Female | Aged | progression of chronic renal failure | polycystic kidney disease | survival | kidney volume | cystic kidney | Basic Research
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7. Full Text Fetal imaging prompts maternal diagnosis: Autosomal dominant polycystic kidney disease
by Euser, A.G and Sung, J.F and Reeves, S
Journal of Perinatology, ISSN 0743-8346, 07/2015, Volume 35, Issue 7, pp. 537 - 538
Autosomal dominant polycystic kidney disease (ADPKD) is a common inherited disorder. Ultrasound (US) findings can include enlarged echogenic kidneys in utero... 
PEDIATRICS | OBSTETRICS & GYNECOLOGY | Polycystic Kidney, Autosomal Dominant - diagnostic imaging | Kidney - diagnostic imaging | Kidney - embryology | Ultrasonography, Prenatal | Humans | Adult | Female | Fetal Diseases - diagnostic imaging | Care and treatment | Diagnosis | Maternal-fetal exchange | Health aspects | Polycystic kidney disease
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8. Full Text Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease
by Rossetti, Sandro and Consugar, Mark B and Chapman, Arlene B and Torres, Vicente E and Guay-Woodford, Lisa M and Grantham, Jared J and Bennett, William M and Meyers, Catherine M and Walker, Denise L and Bae, Kyongtae and Zhang, Qin and Thompson, Paul A and Miller, J. Philip and Harris, Peter C and Crisp Consortium and CRISP Consortium
Journal of the American Society of Nephrology, ISSN 1046-6673, 07/2007, Volume 18, Issue 7, pp. 2143 - 2160
Mutation-based molecular diagnostics of autosomal dominant polycystic kidney disease (ADPKD) is complicated by genetic and allelic heterogeneity, large... 
DOMAIN | ADPKD | PROTEIN | SUBSTITUTIONS | UROLOGY & NEPHROLOGY | PKD1 GENE | MUTATIONS | BRCA1 | SPECTRUM | IDENTIFICATION | KIDNEY-DISEASE-1 | Molecular Diagnostic Techniques | Polycystic Kidney, Autosomal Dominant - genetics | Polycystic Kidney, Autosomal Dominant - diagnosis | Humans | Middle Aged | Adolescent | Adult | Mutation | Sequence Analysis, DNA
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9. Full Text Preimplantation Genetic Diagnosis Counseling in Autosomal Dominant Polycystic Kidney Disease
by Murphy, Erin L and Droher, Madeline L and DiMaio, Miriam S and Dahl, Neera K
American Journal of Kidney Diseases, ISSN 0272-6386, 12/2018, Volume 72, Issue 6, pp. 866 - 872
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common hereditary forms of chronic kidney disease. Mutations within or lead to... 
genetic counseling | assisted reproductive technology | linkage analysis | mutation detection | end-stage renal disease (ESRD) | Autosomal dominant polycystic kidney disease (ADPKD) | preimplantation genetic diagnosis (PGD) | pregnancy | PKD2 | in vitro fertilization (IVF) | PKD1 | in vitro fertilization (IVF) | UROLOGY & NEPHROLOGY | ADPKD | FAMILY-HISTORY | PROGRESSION | VOLUME | Follow-Up Studies | Risk Assessment | Humans | Embryo Implantation - genetics | Preimplantation Diagnosis | Magnetic Resonance Imaging - methods | Genetic Counseling | Genetic Testing - methods | Disease Progression | Pregnancy | Kidney Failure, Chronic - prevention & control | Polycystic Kidney, Autosomal Dominant - diagnosis | Adult | Female | Polycystic Kidney, Autosomal Dominant - complications | Pregnancy Outcome | Kidney Failure, Chronic - etiology
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10. Molecular diagnosis of autosomal dominant polycystic kidney disease
by Song, Xuewen and Haghighi, Amirreza and Iliuta, Ioan-Andrei and Pei, York
Expert Review of Molecular Diagnostics, ISSN 1473-7159, 10/2017, Volume 17, Issue 10, pp. 885 - 895
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease that accounts for 5-10% of end-stage renal... 
PKD2 | PKD1 | Autosomal dominant polycystic kidney disease | Next Generation Sequencing | molecular diagnosis | MUTATION ANALYSIS | GENOTYPE | PATHOLOGY | SOMATIC MOSAICISM | LIVER-DISEASE | IDENTIFICATION | GENOME | ADPKD | GENE | SEQUENCING DATA | PKD2 MUTATIONS | Diagnosis, Differential | Prognosis | Genetic Association Studies | Humans | Genetic Markers | Genetic Testing - methods | TRPP Cation Channels - genetics | Polycystic Kidney, Autosomal Dominant - metabolism | Polycystic Kidney, Autosomal Dominant - mortality | Polycystic Kidney, Autosomal Dominant - genetics | Polycystic Kidney, Autosomal Dominant - diagnosis | High-Throughput Nucleotide Sequencing | Mutation | Genomics - methods | TRPP Cation Channels - metabolism
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11. 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
Background In people with early autosomal dominant polycystic kidney disease (ADPKD), average total kidney volume (TKV) is 3 times normal and increases by an... 
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 | VOLUME PROGRESSION | RENAL-FUNCTION | CYST | LIVER-DISEASE | PAIN | GROWTH | UROLOGY & NEPHROLOGY | OUTCOMES | Polycystic Kidney, Autosomal Dominant - epidemiology | Prospective Studies | Cross-Sectional Studies | Double-Blind Method | Pain - epidemiology | Humans | Middle Aged | Renal Insufficiency, Chronic - psychology | Male | Renal Insufficiency, Chronic - epidemiology | Young Adult | Pain - psychology | Pain Measurement - methods | Polycystic Kidney, Autosomal Dominant - diagnosis | Polycystic Kidney, Autosomal Dominant - psychology | Adolescent | Adult | Female | Renal Insufficiency, Chronic - diagnosis | Surveys and Questionnaires | Quality of Life - psychology | Health Status | Pain - diagnosis | ADPKD | CKD | QoL
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12. Full Text Liver Involvement in Early Autosomal-Dominant Polycystic Kidney Disease
by Hogan, Marie C and Abebe, Kaleab and Torres, Vicente E and Chapman, Arlene B and Bae, Kyongtae T and Tao, Cheng and Sun, Hongliang and Perrone, Ronald D and Steinman, Theodore I and Braun, William and Winklhofer, Franz T and Miskulin, Dana C and Rahbari-Oskoui, Frederic and Brosnahan, Godela and Masoumi, Amirali and Karpov, Irina O and Spillane, Susan and Flessner, Michael and Moore, Charity G and Schrier, Robert W
Clinical Gastroenterology and Hepatology, ISSN 1542-3565, 2015, Volume 13, Issue 1, pp. 155 - 164.e6
Background & Aims Polycystic liver disease (PLD), the most common extrarenal manifestation of autosomal-dominant polycystic kidney disease (ADPKD), has become... 
Gastroenterology and Hepatology | HALT-PKD-A | MRI Analysis | Hepatic Cyst | CKD | MRI analysis | Hepatic cyst | HEPATIC CYSTS | ACQUISITION | ADULTS | COMPUTED-TOMOGRAPHY | NORMAL SPLENIC VOLUME | HYPERTROPHY | IMAGING EVALUATION | SOMATOSTATIN | GASTROENTEROLOGY & HEPATOLOGY | STAGE RENAL-DISEASE | Hepatomegaly - pathology | Liver Function Tests | Cross-Sectional Studies | Humans | Liver | Middle Aged | Male | Randomized Controlled Trials as Topic | Young Adult | Hepatomegaly - epidemiology | Polycystic Kidney, Autosomal Dominant - diagnosis | Adolescent | Adult | Female | Polycystic Kidney, Autosomal Dominant - complications | Charities | Sects | Medical colleges | Liver diseases | Analysis | Mortality | Polycystic kidney disease | hepatic cyst
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13. Full Text Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease
by De Rechter, Stéphanie and Kringen, Jonathan and Janssens, Peter and Liebau, Max Christoph and Devriendt, Koenraad and Levtchenko, Elena and Bergmann, Carsten and Jouret, François and Bammens, Bert and Borry, Pascal and Schaefer, Franz and Mekahli, Djalila
PLoS ONE, ISSN 1932-6203, 09/2017, Volume 12, Issue 9, p. e0185779
Several ethical aspects in the management of Autosomal Dominant Polycystic Kidney Disease (ADPKD) are still controversial, including family planning and... 
INDIVIDUALS | MINORS | ADPKD | MULTIDISCIPLINARY SCIENCES | VOLUME | RISK | RENAL-DISEASE | CHILDREN | Attitude of Health Personnel | Family Planning Services | Polycystic Kidney, Autosomal Dominant - diagnosis | Humans | Middle Aged | Polycystic Kidney, Autosomal Dominant - therapy | Adult | Female | Male | Surveys and Questionnaires | Polycystic Kidney, Autosomal Dominant - physiopathology | Family planning | Physicians | Beliefs, opinions and attitudes | Practice | Research | Diagnosis | Polycystic kidney disease | Pediatrics | Nephrology | Nuclear magnetic resonance--NMR | Transplants & implants | Hemodialysis | Families & family life | Risk | Medical diagnosis | Genetic screening | Ethics | Accuracy | Ultrasonic imaging | Genetics | Hypertension | Statistical analysis | Polycystic kidney | Legal medicine | Health risks | Attitudes | Implantation | Disease control | Pregnancy | Medicine | Offspring | Hospitals | Cysts | Adults | Clinical medicine | Kidney diseases | Kidney transplantation | Nuclear magnetic resonance | NMR
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