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

Year Number of Results
1958 1
1959 2
1963 2
1964 2
1965 1
1967 2
1968 1
1969 2
1971 1
1972 2
1973 2
1974 5
1975 4
1977 2
1978 3
1979 2
1980 2
1981 4
1982 4
1983 1
1984 2
1985 3
1986 2
1987 1
1988 1
1989 1
1991 1
1992 1
2002 2
2003 1
2004 2
2005 4
2006 8
2007 8
2008 15
2009 13
2010 11
2011 15
2012 6
2013 8
2014 14
2015 20
2016 20
2017 25
2018 37
2019 34
2020 42
2021 52
2022 50
2023 42
2024 24

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431 results

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Page 1
Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP).
Nakatani S, Kawano H, Sato M, Hoshino J, Nishio S, Miura K, Sekine A, Suwabe T, Hidaka S, Kataoka H, Ishikawa E, Shimazu K, Uchiyama K, Fujimaru T, Moriyama T, Kurashige M, Shimabukuro W, Hattanda F, Kimura T, Ushio Y, Manabe S, Watanabe H, Mitobe M, Seta K, Shimada Y, Kai H, Katayama K, Ichikawa D, Hayashi H, Hanaoka K, Mochizuki T, Nakanishi K, Tsuchiya K, Horie S, Isaka Y, Muto S; JRP collaborators. Nakatani S, et al. Clin Exp Nephrol. 2024 May 11. doi: 10.1007/s10157-024-02509-3. Online ahead of print. Clin Exp Nephrol. 2024. PMID: 38734869
Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children.
Ueda C, Horinouchi T, Inoki Y, Ichikawa Y, Tanaka Y, Kitakado H, Kondo A, Sakakibara N, Nagano C, Yamamura T, Fujimura J, Kamiyoshi N, Ishimori S, Ninchoji T, Kaito H, Shima Y, Iijima K, Nozu K, Yoshikawa N. Ueda C, et al. Among authors: nozu k. Pediatr Nephrol. 2024 Apr 25. doi: 10.1007/s00467-024-06377-7. Online ahead of print. Pediatr Nephrol. 2024. PMID: 38662234
Nephronophthisis 13 caused by WDR19 variants with pancytopenia: case report.
Tanaka Y, Horinouchi T, Inoki Y, Ichikawa Y, Ueda C, Kitakado H, Kondo A, Sakakibara N, Nagano C, Yano Y, Yoshikawa N, Morisada N, Nozu K. Tanaka Y, et al. Among authors: nozu k. CEN Case Rep. 2024 Apr 8. doi: 10.1007/s13730-024-00871-5. Online ahead of print. CEN Case Rep. 2024. PMID: 38589766 Free article.
A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency.
Nakatani N, Tamura A, Hanafusa H, Nino N, Yamamoto N, Awano H, Tanaka Y, Morisada N, Uemura S, Saito A, Hasegawa D, Nozu K, Kosaka Y. Nakatani N, et al. Among authors: nozu k. Hum Genome Var. 2024 Mar 22;11(1):15. doi: 10.1038/s41439-024-00271-2. Hum Genome Var. 2024. PMID: 38514645 Free PMC article.
431 results