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

Year Number of Results
1976 3
1978 2
1989 1
1996 1
2001 1
2006 2
2007 5
2008 4
2009 5
2010 5
2011 5
2012 9
2013 8
2014 12
2015 10
2016 9
2017 13
2018 16
2019 9
2020 11
2021 7
2022 5
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114 results
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Page 1
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: kaito h. 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.
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: kaito h. 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.
Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial.
Iijima K, Sako M, Nozu K, Mori R, Tuchida N, Kamei K, Miura K, Aya K, Nakanishi K, Ohtomo Y, Takahashi S, Tanaka R, Kaito H, Nakamura H, Ishikura K, Ito S, Ohashi Y; Rituximab for Childhood-onset Refractory Nephrotic Syndrome (RCRNS) Study Group. Iijima K, et al. Among authors: kaito h. Lancet. 2014 Oct 4;384(9950):1273-81. doi: 10.1016/S0140-6736(14)60541-9. Epub 2014 Jun 22. Lancet. 2014. PMID: 24965823 Clinical Trial.
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.
Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Ye MJ, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Morioka I, Nakanishi K, Yoshikawa N, Kaito H, Iijima K. Kamiyoshi N, et al. Among authors: kaito h. Clin J Am Soc Nephrol. 2016 Aug 8;11(8):1441-9. doi: 10.2215/CJN.01000116. Epub 2016 Jun 8. Clin J Am Soc Nephrol. 2016. PMID: 27281700 Free PMC article.
Mycophenolate Mofetil after Rituximab for Childhood-Onset Complicated Frequently-Relapsing or Steroid-Dependent Nephrotic Syndrome.
Iijima K, Sako M, Oba M, Tanaka S, Hamada R, Sakai T, Ohwada Y, Ninchoji T, Yamamura T, Machida H, Shima Y, Tanaka R, Kaito H, Araki Y, Morohashi T, Kumagai N, Gotoh Y, Ikezumi Y, Kubota T, Kamei K, Fujita N, Ohtsuka Y, Okamoto T, Yamada T, Tanaka E, Shimizu M, Horinouchi T, Konishi A, Omori T, Nakanishi K, Ishikura K, Ito S, Nakamura H, Nozu K; Japanese Study Group of Kidney Disease in Children. Iijima K, et al. Among authors: kaito h. J Am Soc Nephrol. 2022 Feb;33(2):401-419. doi: 10.1681/ASN.2021050643. Epub 2021 Dec 8. J Am Soc Nephrol. 2022. PMID: 34880074 Clinical Trial.
Crescentic IgA nephropathy in children.
Shima Y, Nakanishi K, Hama T, Mukaiyama H, Sato M, Tanaka Y, Tanaka R, Kaito H, Nozu K, Sako M, Iijima K, Yoshikawa N. Shima Y, et al. Among authors: kaito h. Pediatr Nephrol. 2020 Jun;35(6):1005-1014. doi: 10.1007/s00467-020-04483-w. Epub 2020 Jan 28. Pediatr Nephrol. 2020. PMID: 31993782
An "old and new" complication in a child with nephrotic syndrome: Answers.
Inaguma Y, Kaito H, Horinouchi T, Ogawa Y, Yoshida M, Yoshikawa N, Tanaka R. Inaguma Y, et al. Among authors: kaito h. Pediatr Nephrol. 2021 Jul;36(7):1955-1958. doi: 10.1007/s00467-020-04794-y. Epub 2020 Oct 14. Pediatr Nephrol. 2021. PMID: 33052450 No abstract available.
An "old and new" complication in a child with nephrotic syndrome: Questions.
Inaguma Y, Kaito H, Horinouchi T, Ogawa Y, Yoshida M, Yoshikawa N, Tanaka R. Inaguma Y, et al. Among authors: kaito h. Pediatr Nephrol. 2021 Jul;36(7):1953-1954. doi: 10.1007/s00467-020-04787-x. Epub 2020 Oct 14. Pediatr Nephrol. 2021. PMID: 33052449 No abstract available.
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases.
Kondo A, Nagano C, Ishiko S, Omori T, Aoto Y, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Nagai S, Okada E, Shima Y, Nakanishi K, Ninchoji T, Kaito H, Takeda H, Nagase H, Morisada N, Iijima K, Nozu K. Kondo A, et al. Among authors: kaito h. Sci Rep. 2021 Aug 9;11(1):16099. doi: 10.1038/s41598-021-95521-6. Sci Rep. 2021. PMID: 34373523 Free PMC article.
114 results