Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1950 6
1955 1
1960 1
1961 1
1962 3
1963 6
1964 7
1965 14
1966 12
1967 8
1968 5
1969 11
1970 7
1971 8
1972 8
1973 9
1974 14
1975 15
1976 13
1977 11
1978 12
1979 15
1980 22
1981 9
1982 15
1983 26
1984 25
1985 20
1986 33
1987 26
1988 29
1989 29
1990 56
1991 29
1992 48
1993 49
1994 48
1995 42
1996 50
1997 54
1998 41
1999 65
2000 61
2001 64
2002 62
2003 65
2004 75
2005 89
2006 92
2007 87
2008 67
2009 82
2010 89
2011 87
2012 90
2013 105
2014 98
2015 74
2016 95
2017 109
2018 105
2019 114
2020 105
2021 132
2022 86
Text availability
Article attribute
Article type
Publication date

Search Results

2,697 results
Results by year
Filters applied: . Clear all
Page 1
IPNA clinical practice recommendations for the diagnosis and management of children with steroid-resistant nephrotic syndrome.
Trautmann A, Vivarelli M, Samuel S, Gipson D, Sinha A, Schaefer F, Hui NK, Boyer O, Saleem MA, Feltran L, Müller-Deile J, Becker JU, Cano F, Xu H, Lim YN, Smoyer W, Anochie I, Nakanishi K, Hodson E, Haffner D; International Pediatric Nephrology Association. Trautmann A, et al. Among authors: nakanishi k. Pediatr Nephrol. 2020 Aug;35(8):1529-1561. doi: 10.1007/s00467-020-04519-1. Epub 2020 May 7. Pediatr Nephrol. 2020. PMID: 32382828 Free PMC article. Review.
Interleukin-18 in Health and Disease.
Yasuda K, Nakanishi K, Tsutsui H. Yasuda K, et al. Among authors: nakanishi k. Int J Mol Sci. 2019 Feb 2;20(3):649. doi: 10.3390/ijms20030649. Int J Mol Sci. 2019. PMID: 30717382 Free PMC article. Review.
A review of clinical characteristics and genetic backgrounds in Alport syndrome.
Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K. Nozu K, et al. Among authors: nakanishi k. Clin Exp Nephrol. 2019 Feb;23(2):158-168. doi: 10.1007/s10157-018-1629-4. Epub 2018 Aug 20. Clin Exp Nephrol. 2019. PMID: 30128941 Free PMC article. Review.
Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.
Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K. Nagano C, et al. Among authors: nakanishi k. Sci Rep. 2020 Jan 14;10(1):270. doi: 10.1038/s41598-019-57149-5. Sci Rep. 2020. PMID: 31937884 Free PMC article.
Clinical and Genetic Characteristics in Patients With Gitelman Syndrome.
Fujimura J, Nozu K, Yamamura T, Minamikawa S, Nakanishi K, Horinouchi T, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Miyako K, Nozu Y, Morisada N, Nagase H, Ninchoji T, Kaito H, Iijima K. Fujimura J, et al. Among authors: nakanishi k. Kidney Int Rep. 2018 Sep 28;4(1):119-125. doi: 10.1016/j.ekir.2018.09.015. eCollection 2019 Jan. Kidney Int Rep. 2018. PMID: 30596175 Free PMC article.
Uric Acid.
Nakanishi K, Morita H. Nakanishi K, et al. Int Heart J. 2022;63(3):423-425. doi: 10.1536/ihj.22-127. Int Heart J. 2022. PMID: 35650143 Free article. No abstract available.
2,697 results