Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1987 2
1994 1
1995 3
1996 1
1997 2
1998 1
1999 1
2002 1
2003 1
2004 1
2005 1
2006 3
2007 1
2008 1
2009 1
2010 2
2011 2
2012 1
2015 2
2017 1
2018 1
2019 1
2022 1
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

32 results

Results by year

Filters applied: . Clear all
Page 1
Hereditary Renal Cystic Disorders: Imaging of the Kidneys and Beyond.
Dillman JR, Trout AT, Smith EA, Towbin AJ. Dillman JR, et al. Radiographics. 2017 May-Jun;37(3):924-946. doi: 10.1148/rg.2017160148. Radiographics. 2017. PMID: 28493804 Review.
The two most common categories of hereditary renal cystic disease are (a) the ciliopathic disorders, which are related to mutations affecting the primary cilia (called "ciliopathies"), and (b) the phakomatoses. Autosomal dominant polycystic kidney dise …
The two most common categories of hereditary renal cystic disease are (a) the ciliopathic disorders, which are related to mutations affectin …
[Guidelines for the management of tuberous sclerosis complex renal disease].
Rouvière O, Nivet H, Grenier N, Zini L, Lechevallier E. Rouvière O, et al. Prog Urol. 2012 Jun;22(7):367-79. doi: 10.1016/j.purol.2012.03.006. Epub 2012 Apr 30. Prog Urol. 2012. PMID: 22657256 Review. French.
PURPOSE: To review existing literature and deduce guidelines for the management of renal disease in patients with tuberous sclerosis complex (TSC). PATIENTS: After review of literature, a core panel of five physicians wrote a draft that was evaluated by 14 reviewers …
PURPOSE: To review existing literature and deduce guidelines for the management of renal disease in patients with tuberous scleros
Ocular manifestations of renal ciliopathies.
Salehi O, Mack H, Colville D, Lewis D, Savige J. Salehi O, et al. Pediatr Nephrol. 2024 May;39(5):1327-1346. doi: 10.1007/s00467-023-06096-5. Epub 2023 Aug 30. Pediatr Nephrol. 2024. PMID: 37644229 Free PMC article. Review.
Ocular abnormalities are not associated with the most common adult-onset "cystic" kidney diseases, namely, autosomal dominant (AD) polycystic kidney disease and the AD tubulointerstitial kidney diseases (ADTKD). However, other kidney
Ocular abnormalities are not associated with the most common adult-onset "cystic" kidney diseases, namely, autosomal domina
Renal cystic diseases.
Thomsen HS, Levine E, Meilstrup JW, Van Slyke MA, Edgar KA, Barth JC, Hartman DS. Thomsen HS, et al. Eur Radiol. 1997;7(8):1267-75. doi: 10.1007/s003300050288. Eur Radiol. 1997. PMID: 9377514 Review.
Because of their diverse etiology, histology, and clinical presentation, no single scheme of classification has gained acceptance. Conditions include autosomal dominant polycystic kidney disease, acquired renal cystic disease, medullary sponge kidne
Because of their diverse etiology, histology, and clinical presentation, no single scheme of classification has gained acceptance. Condition …
Tuberous sclerosis complex renal disease.
Dixon BP, Hulbert JC, Bissler JJ. Dixon BP, et al. Nephron Exp Nephrol. 2011;118(1):e15-20. doi: 10.1159/000320891. Epub 2010 Nov 11. Nephron Exp Nephrol. 2011. PMID: 21071977 Free PMC article. Review.
Although not as common as other genetic renal diseases such as autosomal dominant polycystic kidney disease, patients with tuberous sclerosis complex frequently have significant renal involvement. Recent revelations in the cell biology of …
Although not as common as other genetic renal diseases such as autosomal dominant polycystic kidney disease, pat …
Cystic kidney disease: a primer.
Cramer MT, Guay-Woodford LM. Cramer MT, et al. Adv Chronic Kidney Dis. 2015 Jul;22(4):297-305. doi: 10.1053/j.ackd.2015.04.001. Adv Chronic Kidney Dis. 2015. PMID: 26088074 Review.
In this review, we have categorized renal cystic disease according to inherited single-gene disorders, for example, autosomal recessive polycystic kidney disease; syndromic disorders associated with kidney cysts, for example, tuberous scleros
In this review, we have categorized renal cystic disease according to inherited single-gene disorders, for example, autosomal recessi …
Polycystic kidney disease. 1: Identification and analysis of the primary defect.
Harris PC, Ward CJ, Peral B, Hughes J. Harris PC, et al. J Am Soc Nephrol. 1995 Oct;6(4):1125-33. doi: 10.1681/ASN.V641125. J Am Soc Nephrol. 1995. PMID: 8589278 Review.
The identification of the primary defect in autosomal dominant polycystic kidney disease (ADPKD) by biochemical methods has proved difficult because of the complexity of the cystic kidney. ...However, a number of patients with large deletions of …
The identification of the primary defect in autosomal dominant polycystic kidney disease (ADPKD) by biochemical …
Autosomal recessive and dominant polycystic kidney diseases.
Sessa A, Righetti M, Battini G. Sessa A, et al. Minerva Urol Nefrol. 2004 Dec;56(4):329-38. Minerva Urol Nefrol. 2004. PMID: 15785425 Review.
It is possible to identify renal cysts in several subjects by ultrasonography imaging techniques. Among the inherited polycystic kidney diseases we include autosomal recessive polycystic kidney disease (ARPKD) and autosomal dominant
It is possible to identify renal cysts in several subjects by ultrasonography imaging techniques. Among the inherited polycystic k
Autosomal dominant polycystic kidney disease: clues to pathogenesis.
Harris PC. Harris PC. Hum Mol Genet. 1999;8(10):1861-6. doi: 10.1093/hmg/8.10.1861. Hum Mol Genet. 1999. PMID: 10469838 Review.
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutation of one of two genes: PKD1 (16p13.3) or PKD2 (4q13-23). ...Recently, two further polycystin-like molecules have been identified, indicating roles for this novel protein family be
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutation of one of two genes: PKD1 (16p13.3) o
Polycystic kidney disease: etiology, pathogenesis, and treatment.
Martinez JR, Grantham JJ. Martinez JR, et al. Dis Mon. 1995 Nov;41(11):693-765. doi: 10.1016/s0011-5029(05)80007-0. Dis Mon. 1995. PMID: 7587886 Review.
Polycystic kidney disease (PKD) may be hereditary or acquired. The major inherited types are autosomal dominant (AD) and autosomal recessive (AR). ADPKD is caused by at least two (and possibly three) genes located on separate chromosomes, while
Polycystic kidney disease (PKD) may be hereditary or acquired. The major inherited types are autosomal dominant
32 results