Similar articles for PMID: 29352455

Year	Number of Results
1998	1
2001	1
2002	1
2004	2
2005	1
2007	2
2009	1
2010	5
2011	4
2012	4
2013	5
2014	8
2015	12
2016	12
2017	10
2018	20
2019	14
2020	9
2021	14
2022	21
2023	10
2024	0

1

Clinical features in a series of 258 Japanese pediatric patients with thrombotic microangiopathy.

Ashida A, Matsumura H, Sawai T, Fujimaru R, Fujii Y, Shirasu A, Nakakura H, Iijima K. Ashida A, et al. Clin Exp Nephrol. 2018 Aug;22(4):924-930. doi: 10.1007/s10157-018-1531-0. Epub 2018 Jan 19. Clin Exp Nephrol. 2018. PMID: 29352455

2

A nationwide cross-sectional analysis of thrombotic microangiopathy in the Japan Renal Biopsy Registry (J-RBR).

Katsuno T, Ito Y, Kagami S, Kitamura H, Maruyama S, Shimizu A, Sugiyama H, Sato H, Yokoyama H, Kashihara N. Katsuno T, et al. Clin Exp Nephrol. 2020 Sep;24(9):789-797. doi: 10.1007/s10157-020-01896-7. Epub 2020 May 15. Clin Exp Nephrol. 2020. PMID: 32415379

3

[Diagnosis and treatment of TMA based on Japanese clinical guides].

Wada H, Hasegawa K, Watanabe M. Wada H, et al. Rinsho Ketsueki. 2017;58(7):849-856. doi: 10.11406/rinketsu.58.849. Rinsho Ketsueki. 2017. PMID: 28781284 Japanese.

4

Atypical reduction of plasma ADAMTS13 activity by a non-IgG-type inhibitor in a patient with hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli.

Nakayama S, Hirashio S, Yorishima H, Doi T, Yoshida Y, Matsumoto M, Masaki T. Nakayama S, et al. CEN Case Rep. 2019 Nov;8(4):266-270. doi: 10.1007/s13730-019-00405-4. Epub 2019 Jun 8. CEN Case Rep. 2019. PMID: 31177384 Free PMC article.

5

Safety and effectiveness of eculizumab for pediatric patients with atypical hemolytic-uremic syndrome in Japan: interim analysis of post-marketing surveillance.

Ito S, Hidaka Y, Inoue N, Kaname S, Kato H, Matsumoto M, Miyakawa Y, Mizuno M, Okada H, Shimono A, Matsuda T, Maruyama S, Fujimura Y, Nangaku M, Kagami S. Ito S, et al. Clin Exp Nephrol. 2019 Jan;23(1):112-121. doi: 10.1007/s10157-018-1610-2. Epub 2018 Jul 23. Clin Exp Nephrol. 2019. PMID: 30039480 Free PMC article.

6

Natural history of thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.

Wada H, Matsumoto T, Yamashita Y. Wada H, et al. Semin Thromb Hemost. 2014 Nov;40(8):866-73. doi: 10.1055/s-0034-1395154. Epub 2014 Nov 6. Semin Thromb Hemost. 2014. PMID: 25377323 Review.

7

Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New Zealand.

Fox LC, Cohney SJ, Kausman JY, Shortt J, Hughes PD, Wood EM, Isbel NM, de Malmanche T, Durkan A, Hissaria P, Blombery P, Barbour TD. Fox LC, et al. Nephrology (Carlton). 2018 Jun;23(6):507-517. doi: 10.1111/nep.13234. Nephrology (Carlton). 2018. PMID: 29419916 Review.

8

[Thrombotic microangiopathies in surgical intensive care medicine with special consideration of atypical hemolytic uremic syndrome].

Albrecht S, Kamla CE, Schönermarck U, Wassilowsky D. Albrecht S, et al. Anaesthesiologie. 2023 Jan;72(1):3-12. doi: 10.1007/s00101-022-01221-9. Epub 2022 Dec 1. Anaesthesiologie. 2023. PMID: 36454255 Free PMC article. Review. German.

9

The utility of ADAMTS13 in differentiating TTP from other acute thrombotic microangiopathies: results from the UK TTP Registry.

Hassan S, Westwood JP, Ellis D, Laing C, Mc Guckin S, Benjamin S, Scully M. Hassan S, et al. Br J Haematol. 2015 Dec;171(5):830-5. doi: 10.1111/bjh.13654. Epub 2015 Sep 11. Br J Haematol. 2015. PMID: 26359646 Free article.

10

The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathies.

Phillips EH, Westwood JP, Brocklebank V, Wong EK, Tellez JO, Marchbank KJ, McGuckin S, Gale DP, Connolly J, Goodship TH, Kavanagh D, Scully MA. Phillips EH, et al. J Thromb Haemost. 2016 Jan;14(1):175-85. doi: 10.1111/jth.13189. Epub 2016 Jan 11. J Thromb Haemost. 2016. PMID: 26559391 Free PMC article.

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