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

Year Number of Results
1983 1
1985 3
1990 1
1992 2
1993 1
1994 1
1998 1
2000 1
2006 1
2008 1
2009 6
2010 6
2011 7
2012 6
2013 4
2014 6
2015 2
2016 1
2018 2
2019 3
2020 4
2021 3
2022 2
2024 1

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56 results

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Page 1
Characterization of the Aeration and Hydrodynamics in Vertical-Wheel™ Bioreactors.
Neto PM, Nogueira DES, Hashimura Y, Jung S, Pedras B, Berberan-Santos MN, Palmeira T, Lee B, Cabral JMS, Geraldes V, Rodrigues CAV. Neto PM, et al. Among authors: hashimura y. Bioengineering (Basel). 2022 Aug 12;9(8):386. doi: 10.3390/bioengineering9080386. Bioengineering (Basel). 2022. PMID: 36004911 Free PMC article.
Segmental membranous nephropathy with severe IgG3 deposition.
Kondo A, Hashimura Y, Uchiyama T, Yoshikawa N, Minami H. Kondo A, et al. Among authors: hashimura y. Pediatr Int. 2018 Jun;60(6):597-598. doi: 10.1111/ped.13560. Epub 2018 May 9. Pediatr Int. 2018. PMID: 29744961 No abstract available.
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. 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.
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.
Jia X, Yamamura T, Gbadegesin R, McNulty MT, Song K, Nagano C, Hitomi Y, Lee D, Aiba Y, Khor SS, Ueno K, Kawai Y, Nagasaki M, Noiri E, Horinouchi T, Kaito H, Hamada R, Okamoto T, Kamei K, Kaku Y, Fujimaru R, Tanaka R, Shima Y; Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan; Baek J, Kang HG, Ha IS, Han KH, Yang EM; Korean Consortium of Hereditary Renal Diseases in Children; Abeyagunawardena A, Lane B, Chryst-Stangl M, Esezobor C, Solarin A; Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group); Dossier C, Deschênes G; NEPHROVIR; Vivarelli M, Debiec H, Ishikura K, Matsuo M, Nozu K, Ronco P, Cheong HI, Sampson MG, Tokunaga K, Iijima K. Jia X, et al. Kidney Int. 2020 Nov;98(5):1308-1322. doi: 10.1016/j.kint.2020.05.029. Epub 2020 Jun 14. Kidney Int. 2020. PMID: 32554042 Free PMC article.
56 results