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1. Full Text Mineral bone disease in autosomal dominant polycystic kidney disease
by Gitomer, Berenice and Pereira, Renata and Salusky, Isidro B and Stoneback, Jason W and Isakova, Tamara and Cai, Xuan and Dalrymple, Lorien S and Ofsthun, Norma and You, Zhiying and Malluche, Harmut H and Maddux, Franklin and George, Diana and Torres, Vicente and Chapman, Arlene and Steinman, Theodore I and Wolf, Myles and Chonchol, Michel
Kidney international, ISSN 0085-2538, 09/2020
Index Medicus
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2. Full Text Rapidly progressive nephromegaly in a neonate with autosomal recessive poly cystic kidney disease
by Naseri, Mitra and Zabolinejad, Nona and Alamdaran, Syed Ali and Shojaeian, Reza
Journal of nephropathology, ISSN 2251-8363, 2017, Volume 6, Issue 4, pp. 363 - 367
Nephromegaly | ADPKD | ARPKD | Childhood
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3. Full Text 18F-FDG PET/CT in autosomal dominant polycystic kidney disease patients with suspected cyst infection
by Pijl, Jordy P and Glaudemans, Andor W.J.M and Slart, Riemer H.J.A and Kwee, Thomas C
Journal of Nuclear Medicine, ISSN 0161-5505, 11/2018, Volume 59, Issue 11, pp. 1734 - 1741
Infection | Infectious disease | ADPKD | Kidney | Cyst | PET/CT | Index Medicus
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4. New advances in the etiopathogenesis of the autosomal dominant polycystic kidney disease
by Hrčková, Gabriela and Skalická, Katarína and Kovács, László
Aktuality v nefrologii, ISSN 1210-955X, 2018, Volume 24, Issue 1, pp. 29 - 33
Polycystins | ADPKD | Cystogenesis | Calcium
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5. Full Text European ADPKD Forum multidisciplinary position statement on autosomal dominant polycystic kidney disease care: European ADPKD Forum and Multispecialist Roundtable participants
by Harris, Tess and Sandford, Richard and de Coninck, Brenda and Devuyst, Olivier and nth, Joost P H and Ecder, Tevfik and Kent, Alastair and Gansevoort, Ron T and Górriz, José Luis and Ong, Albert C M and Pirson, Yves and Torres, Vicente E and Budde, Klemens and Clément, Denis and Derchi, Lorenzo E and Eleftheroudi, Marianna and Levtchenko, Elena and Peters, Dorien and Van Poppel, Henik and Vanholder, Raymond and Roundtable participants and EAF members and EAF co-chairs
Nephrology, dialysis, transplantation, ISSN 0931-0509, 04/2018, Volume 33, Issue 4, pp. 563 - 573
MANAGEMENT | INTRACRANIAL ANEURYSMS | PATIENT PERSPECTIVES | PERITONEAL-DIALYSIS | PREVALENCE | QUALITY-OF-LIFE | RENAL REPLACEMENT THERAPY | ERA-EDTA REGISTRY | CLINICAL-PRACTICE | Journal Article | BLOOD-PRESSURE | clinical practice | ADPKD | polycystic kidney disease | CKD | multispecialist care | Editor's Choice | Special Report
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6. Full Text Plasma metabolites and lipids associate with kidney function and kidney volume in hypertensive ADPKD patients early in the disease course 11 Medical and Health Sciences 1103 Clinical Sciences
by Kim, Kyoungmi and Trott, Josephine F and Gao, Guimin and Chapman, Arlene and Weiss, Robert H
BMC nephrology, 02/2019, Volume 20, Issue 1
Progression | Metabolomics | ADPKD | HALT study
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7. Full Text ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies
by Bergmann, Carsten
Pediatric nephrology (Berlin, West), ISSN 0931-041X, 1/2015, Volume 30, Issue 1, pp. 15 - 30
Pediatrics | Joubert syndrome and related disorders | Nephronophthisis | Next-generation sequencing | Medicine & Public Health | HNF1ß | Ciliopathies | Polycystic kidney disease (ADPKD/ARPKD) | Bardet–Biedl syndrome | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Phenotype | Polycystic Kidney, Autosomal Dominant - classification | Polycystic Kidney, Autosomal Recessive - classification | Polycystic Kidney, Autosomal Dominant - genetics | Humans | Polycystic Kidney, Autosomal Recessive - genetics | Care and treatment | Diagnosis | Polycystic kidney disease | Index Medicus | ARPKD | Polycystic kidney disease (ADPKD | Review
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8. Full Text Low-Osmolar Diet and Adjusted Water Intake for Vasopressin Reduction in Autosomal Dominant Polycystic Kidney Disease: A Pilot Randomized Controlled Trial
by Amro, Osama W., MD, MS and Paulus, Jessica K., ScD and Noubary, Farzad, PhD and Perrone, Ronald D., MD
American journal of kidney diseases, ISSN 0272-6386, 2016, Volume 68, Issue 6, pp. 882 - 891
Nephrology | copeptin | clinical trial | nutrition | osmolality | salt | Autosomal dominant polycystic kidney disease (ADPKD) | vasopressin | protein | water | urea | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Polycystic Kidney, Autosomal Dominant - urine | Humans | Middle Aged | Drinking | Male | Polycystic Kidney, Autosomal Dominant - diet therapy | Young Adult | Pilot Projects | Osmolar Concentration | Arginine Vasopressin - metabolism | Adolescent | Arginine Vasopressin - urine | Adult | Female | Index Medicus | Water | Salt | Urea | ADPKD | Nutrition | Clinical Trial | Osmolality | Vasopressin | Protein | Copeptin
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9. Full Text Salt, but not protein intake, is associated with accelerated disease progression in autosomal dominant polycystic kidney disease
by Kramers, Bart J and Koorevaar, Iris W and Drenth, Joost P.H and de Fijter, Johan W and Neto, Antonio Gomes and Peters, Dorien J.M and Vart, Priya and Wetzels, Jack F and Zietse, Robert and Gansevoort, Ron T and Meijer, Esther
Kidney international, ISSN 0085-2538, 10/2020, Volume 98, Issue 4, pp. 989 - 998
ADPKD | salt | vasopressin | urea | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Index Medicus
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10. Full Text Characteristics of Patients with End-Stage Kidney Disease in ADPKD
by Shukoor, Shehbaz S and Vaughan, Lisa E and Edwards, Marie E and Lavu, Sravanthi and Kline, Timothy L and Senum, Sarah R and Mkhaimer, Yaman and Zaatari, Ghaith and Irazabal, Maria V and Neal, Reem and Hogan, Marie C and Zoghby, Ziad M and Harris, Peter C and Torres, Vicente E and Chebib, Fouad T
Kidney international reports, ISSN 2468-0249, 12/2020
Characteristics of ESKD in ADPKD | ADPKD | ESKD | Aging | Total Kidney Volume | Gender | TKV | Polycystic Kidney Disease
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11. Full Text Total Kidney Volume in Autosomal Dominant Polycystic Kidney Disease: A Biomarker of Disease Progression and Therapeutic Efficacy
by Alam, Ahsan, MD and Dahl, Neera K., MD and Lipschutz, Joshua H., MD and Rossetti, Sandro, MD and Smith, Patricia, PhD and Sapir, Daniel, MD and Weinstein, Jordan, MD and McFarlane, Philip, MD and Bichet, Daniel G., MD
American journal of kidney diseases, ISSN 0272-6386, 2015, Volume 66, Issue 4, pp. 564 - 576
Nephrology | ADPKD biomarker | decline in renal function | outcome measure | Total kidney volume (TKV) | decreased renal function | cystogenesis | autosomal dominant polycystic kidney disease (ADPKD) | disease progression | decreased kidney function | renal cyst | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Severity of Illness Index | Prognosis | Risk Assessment | Humans | Polycystic Kidney, Autosomal Dominant - therapy | Polycystic Kidney, Autosomal Dominant - pathology | Male | Organ Size - physiology | Biomarkers - blood | Glomerular Filtration Rate - physiology | Disease Progression | Kidney Function Tests | Polycystic Kidney, Autosomal Dominant - genetics | Female | Index Medicus
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12. Full Text Expression and secretion of CXCL12 are enhanced in autosomal dominant polycystic kidney disease
by Hyunho Kim and and Jinmo Sung and Hyunsuk Kim and Hyunjin Ryu and Hayne Cho Park and Yun Kyu Oh and Hyun-seob Lee and Kook-hwan Oh and Curie Ahn
BMB reports, ISSN 1976-6696, 07/2019, Volume 52, Issue 7, pp. 463 - 468
CXCR4 | CXCL12 | hTERT | Autosomal dominant polycystic kidney disease (ADPKD) | Cyst
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13. Full Text Young Women With Polycystic Liver Disease Respond Best to Somatostatin Analogues: A Pooled Analysis of Individual Patient Data
by Gevers, Tom J.G and Inthout, Joanna and Caroli, Anna and Ruggenenti, Piero and Hogan, Marie C and Torres, Vicente E and Nevens, Frederik and Drenth, Joost P.H
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2013, Volume 145, Issue 2, pp. 357 - 365.e2
Gastroenterology and Hepatology | Liver Cysts | ADPKD | PCLD | Drug Therapy | Liver Cysts PCLD ADPKD Drug Therapy | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Cysts - drug therapy | Liver - pathology | Somatostatin - analogs & derivatives | Humans | Middle Aged | Liver Diseases - pathology | Organ Size | Linear Models | Male | Treatment Outcome | Octreotide - therapeutic use | Cysts - pathology | Randomized Controlled Trials as Topic | Peptides, Cyclic - therapeutic use | Adult | Female | Aged | Liver Diseases - drug therapy | Somatostatin - therapeutic use | Polycystic Kidney, Autosomal Dominant - drug therapy | Hypertension | Continuing medical education | Liver diseases | Biomedical engineering | Index Medicus | Abridged Index Medicus
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14. Full Text Divergent function of polycystin 1 and polycystin 2 in cell size regulation
by Viau, Amandine and Kotsis, Fruzsina and Boehlke, Christopher and Braeg, Simone and Klein, Marinella and Nitschke, Roland and Walz, Gerd and Kuehn, E. Wolfgang
Biochemical and biophysical research communications, ISSN 0006-291X, 01/2020, Volume 521, Issue 2, pp. 290 - 295
Polycystins | mTOR | ADPKD | Flow | Cilia | Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Index Medicus
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15. Full Text The positive effect of selective prostaglandin E2 receptor EP2 and EP4 blockade on cystogenesis in vitro is counteracted by increased kidney inflammation in vivo
by Lannoy, Morgane and Valluru, Manoj K and Chang, Lijun and Abdela-Ali, Fatima and Peters, Dorien J.M and Streets, Andrew J and Ong, Albert C.M
Kidney international, ISSN 0085-2538, 08/2020, Volume 98, Issue 2, pp. 404 - 419
cyclic AMP | ADPKD | macrophages | inflammation | prostaglandin E2 | cystogenesis | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Index Medicus
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