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 Custom Filters

Results by year

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

Year Number of Results
1840 2
1841 3
1842 4
1844 2
1845 3
1846 3
1847 4
1848 10
1849 9
1850 7
1851 11
1852 20
1853 14
1854 6
1855 4
1856 10
1857 2
1858 12
1859 4
1860 8
1861 2
1862 7
1863 6
1864 3
1865 5
1866 3
1867 11
1868 7
1869 10
1870 13
1871 2
1872 12
1873 5
1874 10
1875 4
1876 4
1877 6
1878 7
1879 6
1880 6
1881 5
1882 10
1883 7
1884 9
1885 6
1886 11
1887 12
1888 8
1889 16
1890 13
1891 16
1892 22
1893 21
1894 22
1895 11
1896 22
1897 24
1898 9
1899 10
1900 13
1901 4
1902 8
1903 11
1904 16
1905 4
1906 3
1907 6
1908 1
1909 2
1910 3
1911 3
1912 3
1913 1
1914 2
1915 4
1916 2
1917 5
1918 3
1919 3
1921 2
1922 1
1923 5
1945 6
1946 66
1947 71
1948 43
1949 27
1950 24
1951 48
1952 11
1953 11
1954 12
1955 8
1956 5
1957 6
1958 8
1959 10
1960 21
1961 10
1962 10
1963 12
1964 17
1965 164
1966 158
1967 203
1968 237
1969 266
1970 296
1971 186
1972 156
1973 169
1974 199
1975 552
1976 526
1977 532
1978 444
1979 473
1980 472
1981 531
1982 553
1983 631
1984 698
1985 789
1986 822
1987 860
1988 856
1989 877
1990 926
1991 906
1992 949
1993 879
1994 891
1995 1037
1996 1123
1997 1163
1998 1142
1999 1217
2000 1333
2001 1383
2002 1529
2003 1635
2004 1784
2005 1741
2006 1831
2007 1882
2008 2087
2009 2108
2010 2321
2011 2594
2012 2853
2013 3057
2014 3170
2015 3120
2016 2547
2017 2212
2018 2553
2019 2640
2020 3005
2021 3237
2022 3260
2023 3291
2024 3559
2025 3431
2026 171

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

80,798 results

Results by year

Filters applied: . Clear all
Page 1
Dent's disease.
Devuyst O, Thakker RV. Devuyst O, et al. Orphanet J Rare Dis. 2010 Oct 14;5:28. doi: 10.1186/1750-1172-5-28. Orphanet J Rare Dis. 2010. PMID: 20946626 Free PMC article. Review.
Dent's disease is a renal tubular disorder characterized by manifestations of proximal tubule dysfunction, including low-molecular-weight proteinuria, hypercalciuria, nephrolithiasis, nephrocalcinosis, and progressive renal failure. ...Antenatal diagnosis and pre-im …
Dent's disease is a renal tubular disorder characterized by manifestations of proximal tubule dysfunction, including low-molec …
Dent's disease: An unusual cause of kidney failure.
Leite de Sousa L, Pimenta G, Veríssimo R, Carvalho TJ, Laranjinha I. Leite de Sousa L, et al. Clin Nephrol Case Stud. 2023 Jan 12;11:1-5. doi: 10.5414/CNCS110975. eCollection 2023. Clin Nephrol Case Stud. 2023. PMID: 36688186 Free PMC article.
Dent's disease is an X-linked recessive disease characterized by proximal tubulopathy with low-molecular weight proteinuria, hypercalciuria, nephrolithiasis, nephrocalcinosis, and kidney failure. ...This case highlights the importance of considering the diagnosis of …
Dent's disease is an X-linked recessive disease characterized by proximal tubulopathy with low-molecular weight proteinuria, h …
Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis.
Thakker RV. Thakker RV. Kidney Int. 2000 Mar;57(3):787-93. doi: 10.1046/j.1523-1755.2000.00916.x. Kidney Int. 2000. PMID: 10720930 Free article. Review.
An X-linked inheritance for XRN was established by studies of a North American kindred, and a similar inheritance for Dent's disease was indicated by the observation of a greater disease severity in males and an absence of male-to-male transmission in five British f …
An X-linked inheritance for XRN was established by studies of a North American kindred, and a similar inheritance for Dent's d …
Dent's disease.
Neild GH, Thakker RV, Unwin RJ, Wrong OM. Neild GH, et al. Nephrol Dial Transplant. 2005 Oct;20(10):2284-5. doi: 10.1093/ndt/gfh968. Epub 2005 Jul 19. Nephrol Dial Transplant. 2005. PMID: 16030051 No abstract available.
Dent's disease.
Bald M, Vester U, Wingen AM. Bald M, et al. Nephrol Dial Transplant. 2002 Mar;17(3):520-1. doi: 10.1093/ndt/17.3.520. Nephrol Dial Transplant. 2002. PMID: 11865109 No abstract available.
Dent's Disease: A Cause of Monogenic Kidney Stones and Nephrocalcinosis.
Diéguez L, Pilco M, Butori S, Kanashiro A, Balaña J, Emiliani E, Somani BK, Angerri O. Diéguez L, et al. J Pers Med. 2024 Jun 11;14(6):623. doi: 10.3390/jpm14060623. J Pers Med. 2024. PMID: 38929844 Free PMC article.
A small percentage are of monogenic origin, such as Dent's disease (DD). DD is a syndrome that causes low-molecular-weight proteinuria, hypercalciuria, nephrolithiasis, and nephrocalcinosis. ...
A small percentage are of monogenic origin, such as Dent's disease (DD). DD is a syndrome that causes low-molecular-weight pro …
Dent's disease: case series from a single center.
Yaşar H, Leventoğlu E, Büyükkaragöz B, Fidan K, Bakkaloğlu SA, Söylemezoğlu O. Yaşar H, et al. Turk J Pediatr. 2024 Nov 16;66(5):649-657. doi: 10.24953/turkjpediatr.2024.4556. Turk J Pediatr. 2024. PMID: 39582457 Free article.
BACKGROUND: Dent's disease (DD) is a rare X-linked recessive tubulopathy characterized by low molecular weight proteinuria, hypercalciuria, nephrocalcinosis/nephrolithiasis and chronic kidney disease. ...
BACKGROUND: Dent's disease (DD) is a rare X-linked recessive tubulopathy characterized by low molecular weight proteinuria, hy …
[Dent's disease].
Igarashi T. Igarashi T. Nihon Rinsho. 2006 Jun 28;Suppl 2:108-12. Nihon Rinsho. 2006. PMID: 16817362 Review. Japanese. No abstract available.
[Dent's disease].
Pavićević S, Bogdanović R, Ludwig M, Samardzić M. Pavićević S, et al. Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:312-5. doi: 10.2298/sarh08s4312p. Srp Arh Celok Lek. 2008. PMID: 20804101 Free article. Serbian.
INTRODUCTION: Dent disease is X-linked recessive proximal tubulopathy, due to mutations in the CLCN5 gene. ...Except hypercalciuria, which was registered in the patient's mother, all other analyses performed in family members were between reference values. ...
INTRODUCTION: Dent disease is X-linked recessive proximal tubulopathy, due to mutations in the CLCN5 gene. ...Except hypercalciuria, …
ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.
Lourdel S, Grand T, Burgos J, González W, Sepúlveda FV, Teulon J. Lourdel S, et al. Pflugers Arch. 2012 Feb;463(2):247-56. doi: 10.1007/s00424-011-1052-0. Epub 2011 Nov 15. Pflugers Arch. 2012. PMID: 22083641 Review.
Dent's disease is an X-linked recessive disorder affecting the proximal tubules. Mutations in the 2Cl(-)/H(+) exchanger ClC-5 gene CLCN5 are frequently associated with Dent's disease. Functional characterization of mutations of CLCN5 have helped to elu …
Dent's disease is an X-linked recessive disorder affecting the proximal tubules. Mutations in the 2Cl(-)/H(+) exchanger ClC-5 …
80,798 results
You have reached the last available page of results. Please see the User Guide for more information.