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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 2
1968 3
1970 4
1971 7
1972 1
1973 5
1974 4
1975 3
1976 7
1977 3
1979 4
1981 5
1982 7
1983 7
1984 5
1985 11
1986 6
1987 11
1988 20
1989 28
1990 17
1991 25
1992 37
1993 39
1994 36
1995 42
1996 47
1997 55
1998 47
1999 39
2000 35
2001 36
2002 31
2003 46
2004 53
2005 46
2006 75
2007 58
2008 59
2009 52
2010 61
2011 75
2012 59
2013 88
2014 100
2015 92
2016 83
2017 88
2018 74
2019 79
2020 106
2021 98
2022 65
2023 83
2024 26

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1,996 results

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Page 1
Polycystic kidney disease.
Bergmann C, Guay-Woodford LM, Harris PC, Horie S, Peters DJM, Torres VE. Bergmann C, et al. Nat Rev Dis Primers. 2018 Dec 6;4(1):50. doi: 10.1038/s41572-018-0047-y. Nat Rev Dis Primers. 2018. PMID: 30523303 Free PMC article. Review.
Cystic kidneys are common causes of end-stage renal disease, both in children and in adults. Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) are cilia-related disorders …
Cystic kidneys are common causes of end-stage renal disease, both in children and in adults. Autosomal dominant polycystic
Update and review of adult polycystic kidney disease.
Colbert GB, Elrggal ME, Gaur L, Lerma EV. Colbert GB, et al. Dis Mon. 2020 May;66(5):100887. doi: 10.1016/j.disamonth.2019.100887. Epub 2019 Sep 30. Dis Mon. 2020. PMID: 31582186 Review.
Autosomal dominant polycystic kidney disease is a common cause of end stage kidney disease. ...This review updates the clinician on the pathophysiology, clinical aspects, and therapeutic options for patients the is form of kidney disea
Autosomal dominant polycystic kidney disease is a common cause of end stage kidney disease. ...This revie …
Autosomal dominant polycystic kidney disease.
Cornec-Le Gall E, Alam A, Perrone RD. Cornec-Le Gall E, et al. Lancet. 2019 Mar 2;393(10174):919-935. doi: 10.1016/S0140-6736(18)32782-X. Epub 2019 Feb 25. Lancet. 2019. PMID: 30819518 Review.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and one of the most common causes of end-stage kidney disease. ...Phase 3 randomised, placebo-controlled clinical trials have clarifi …
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and one …
Ciliopathies and the Kidney: A Review.
McConnachie DJ, Stow JL, Mallett AJ. McConnachie DJ, et al. Am J Kidney Dis. 2021 Mar;77(3):410-419. doi: 10.1053/j.ajkd.2020.08.012. Epub 2020 Oct 9. Am J Kidney Dis. 2021. PMID: 33039432 Free article. Review.
This group of overlapping and genetically heterogeneous diseases includes polycystic kidney disease, nephronophthisis, and Bardet-Biedl syndrome as the main focus of this review. ...Due to cystic-associated kidney injury and systemic inflammatio …
This group of overlapping and genetically heterogeneous diseases includes polycystic kidney disease, nephronopht …
Polycystic Kidney/Liver Disease.
Roediger R, Dieterich D, Chanumolu P, Deshpande P. Roediger R, et al. Clin Liver Dis. 2022 May;26(2):229-243. doi: 10.1016/j.cld.2022.01.009. Epub 2022 Apr 1. Clin Liver Dis. 2022. PMID: 35487607 Review.
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder that leads to chronic kidney disease and end-stage kidney disease (ESKD). Polycystic liver disease (PCLD) is the most common extrarenal manife …
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder that leads to chronic kidney disea
Autophagy in kidney homeostasis and disease.
Tang C, Livingston MJ, Liu Z, Dong Z. Tang C, et al. Nat Rev Nephrol. 2020 Sep;16(9):489-508. doi: 10.1038/s41581-020-0309-2. Epub 2020 Jul 23. Nat Rev Nephrol. 2020. PMID: 32704047 Free PMC article. Review.
Dysregulated autophagy contributes to the pathogenesis of acute kidney injury, to incomplete kidney repair after acute kidney injury and to chronic kidney disease of varied aetiologies, including diabetic kidney disease, focal segm …
Dysregulated autophagy contributes to the pathogenesis of acute kidney injury, to incomplete kidney repair after acute kidn
Polycystic kidney disease.
Harris PC, Torres VE. Harris PC, et al. Annu Rev Med. 2009;60:321-37. doi: 10.1146/annurev.med.60.101707.125712. Annu Rev Med. 2009. PMID: 18947299 Free PMC article. Review.
A number of inherited disorders result in renal cyst development. The most common form, autosomal dominant polycystic kidney disease (ADPKD), is a disorder most often diagnosed in adults and caused by mutation in PKD1 or PKD2. ...ARPKD is the neonatal form of …
A number of inherited disorders result in renal cyst development. The most common form, autosomal dominant polycystic kidney
Autosomal dominant tubulointerstitial kidney disease.
Devuyst O, Olinger E, Weber S, Eckardt KU, Kmoch S, Rampoldi L, Bleyer AJ. Devuyst O, et al. Nat Rev Dis Primers. 2019 Sep 5;5(1):60. doi: 10.1038/s41572-019-0109-9. Nat Rev Dis Primers. 2019. PMID: 31488840 Review.
Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a recently defined entity that includes rare kidney diseases characterized by tubular damage and interstitial fibrosis in the absence of glomerular lesions, with inescapable progression to …
Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a recently defined entity that includes rare kidney
Polycystic kidney disease: novel insights into polycystin function.
Luo L, Roy S, Li L, Ma M. Luo L, et al. Trends Mol Med. 2023 Apr;29(4):268-281. doi: 10.1016/j.molmed.2023.01.005. Epub 2023 Feb 15. Trends Mol Med. 2023. PMID: 36805211 Review.
Autosomal dominant polycystic kidney disease (ADPKD) is a life-threatening monogenic disease caused by mutations in PKD1 and PKD2 that encode polycystin 1 (PC1) and polycystin 2 (PC2). ...
Autosomal dominant polycystic kidney disease (ADPKD) is a life-threatening monogenic disease caused by mutations …
Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference.
Guay-Woodford LM, Bissler JJ, Braun MC, Bockenhauer D, Cadnapaphornchai MA, Dell KM, Kerecuk L, Liebau MC, Alonso-Peclet MH, Shneider B, Emre S, Heller T, Kamath BM, Murray KF, Moise K, Eichenwald EE, Evans J, Keller RL, Wilkins-Haug L, Bergmann C, Gunay-Aygun M, Hooper SR, Hardy KK, Hartung EA, Streisand R, Perrone R, Moxey-Mims M. Guay-Woodford LM, et al. J Pediatr. 2014 Sep;165(3):611-7. doi: 10.1016/j.jpeds.2014.06.015. Epub 2014 Jul 9. J Pediatr. 2014. PMID: 25015577 Free PMC article.
Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is a severe, typically early onset form of cystic disease that primarily involves the kidneys and biliary tract. ...The meeting was funded by the National Institutes of Health and an edu …
Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is a severe, typically early onset form of cystic …
1,996 results