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

Year Number of Results
1840 2
1841 4
1842 4
1844 2
1845 4
1846 3
1847 6
1848 14
1849 10
1850 7
1851 12
1852 21
1853 14
1854 7
1855 5
1856 12
1857 3
1858 14
1859 6
1860 13
1861 2
1862 9
1863 6
1864 3
1865 5
1866 3
1867 12
1868 8
1869 15
1870 15
1871 3
1872 12
1873 5
1874 10
1875 5
1876 4
1877 9
1878 8
1879 7
1880 9
1881 8
1882 11
1883 13
1884 11
1885 7
1886 11
1887 14
1888 10
1889 16
1890 15
1891 18
1892 24
1893 26
1894 26
1895 12
1896 26
1897 27
1898 12
1899 14
1900 15
1901 6
1902 8
1903 12
1904 18
1905 5
1906 17
1907 22
1908 2
1909 3
1910 4
1911 3
1912 3
1913 1
1914 2
1915 4
1916 3
1917 6
1918 4
1919 5
1920 2
1921 3
1922 2
1923 7
1945 6
1946 66
1947 71
1948 43
1949 28
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 172
1974 201
1975 561
1976 529
1977 534
1978 445
1979 474
1980 478
1981 532
1982 553
1983 631
1984 698
1985 789
1986 823
1987 867
1988 881
1989 913
1990 1010
1991 993
1992 1044
1993 975
1994 969
1995 1129
1996 1212
1997 1266
1998 1238
1999 1307
2000 1439
2001 1498
2002 1620
2003 1728
2004 1877
2005 1872
2006 1945
2007 2021
2008 2230
2009 2240
2010 2474
2011 2771
2012 3056
2013 3248
2014 3409
2015 3336
2016 2827
2017 2527
2018 2842
2019 2984
2020 3379
2021 3582
2022 3600
2023 3583
2024 1432

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81,410 results

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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
Pediatric Endodontics.
Goyal V. Goyal V. Int J Clin Pediatr Dent. 2022;15(Suppl 1):S1-S2. doi: 10.5005/jp-journals-10005-2336. Int J Clin Pediatr Dent. 2022. PMID: 35645490 Free PMC article.
How to cite this article: Goyal V. Pediatric Endodontics. Int J Clin Pediatr Dent 2022;15(S-1):S1-S2....
How to cite this article: Goyal V. Pediatric Endodontics. Int J Clin Pediatr Dent 2022;15(S-1):S1-S2....
Pan-dent-emic: a dentist's dilemma in the COVID-19 era.
Manaktala N, Pralhad S, M R. Manaktala N, et al. Patient Saf Surg. 2021 Feb 14;15(1):9. doi: 10.1186/s13037-021-00282-w. Patient Saf Surg. 2021. PMID: 33583423 Free PMC article.
The present article attempts to explain the dilemma of the current situation from a dentist's perspective. Since, the effects of the contagion are seen across each level of dentistry, the current situation can truly be termed as a "Pan-dent-emic"....
The present article attempts to explain the dilemma of the current situation from a dentist's perspective. Since, the effects of the …
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
Clinical and genetic characteristics of Dent's disease type 1 in Europe.
Burballa C, Cantero-Recasens G, Prikhodina L, Lugani F, Schlingmann K, Ananin PV, Besouw M, Bockenhauer D, Madariaga L, Bertholet-Thomas A, Taroni F, Parolin M, Conlon P, Emma F, Del Prete D, Chauveau D, Koster-Kamphuis L, Fila M, Pasini A, Castro I, Colussi G, Gil M, Mohidin B, Wlodkowski T, Schaefer F, Ariceta G; DENT study group. Burballa C, et al. Nephrol Dial Transplant. 2023 May 31;38(6):1497-1507. doi: 10.1093/ndt/gfac310. Nephrol Dial Transplant. 2023. PMID: 36441012
BACKGROUND: Dent's disease type 1 (DD1) is a rare X-linked nephropathy caused by CLCN5 mutations, characterized by proximal tubule dysfunction, including low molecular weight proteinuria (LMWP), hypercalciuria, nephrolithiasis-nephrocalcinosis, progressive chronic k …
BACKGROUND: Dent's disease type 1 (DD1) is a rare X-linked nephropathy caused by CLCN5 mutations, characterized by proximal tu …
The maize Ga1-s allele confers protection against ga1 pollen in popcorn and dent corn.
Moran Lauter AN, Edwards JW, Scott MP. Moran Lauter AN, et al. Sci Rep. 2022 Dec 2;12(1):20809. doi: 10.1038/s41598-022-25261-8. Sci Rep. 2022. PMID: 36460744 Free PMC article.
Ga1-s can be transferred into dent corn but the effectiveness of the Ga1-s allele in popcorn and dent corn has never been compared, which is important because each are regulated differently regarding GMO contamination. ...While both popcorn and Ga1- …
Ga1-s can be transferred into dent corn but the effectiveness of the Ga1-s allele in popcorn and dent corn has n …
Update on Dent Disease.
Ehlayel AM, Copelovitch L. Ehlayel AM, et al. Pediatr Clin North Am. 2019 Feb;66(1):169-178. doi: 10.1016/j.pcl.2018.09.003. Pediatr Clin North Am. 2019. PMID: 30454742 Review.
Mutations in both the CLCN5 and OCRL1 genes have been associated with the Dent phenotype and are now classified as Dent-1 and Dent-2, respectively. This article describes the clinical presentation, laboratory evaluation, genetics, pathophysiology, management, …
Mutations in both the CLCN5 and OCRL1 genes have been associated with the Dent phenotype and are now classified as Dent-1 and …
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
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.
As a first step in this approach, the chromosomal locations of two disorders referred to as Dent's disease and X-linked recessive nephrolithiasis (XRN) were determined. ...X-linked polymorphic genetic markers were used in linkage studies of these families, and the g …
As a first step in this approach, the chromosomal locations of two disorders referred to as Dent's disease and X-linked recess …
Editorial.
Chalasani S. Chalasani S. Int J Clin Pediatr Dent. 2021;14(Suppl 1):S1. doi: 10.5005/jp-journals-10005-2052. Int J Clin Pediatr Dent. 2021. PMID: 35082457 Free PMC article.
How to cite this article: Chalasani S. Editorial. Int J Clin Pediatr Dent 2021;14(S-1):S1....
How to cite this article: Chalasani S. Editorial. Int J Clin Pediatr Dent 2021;14(S-1):S1....
81,410 results
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