PubMed for id: 414541

Year	Number of Results
1999	1
2001	1
2002	1
2003	2
2004	1
2005	1
2006	3
2007	5
2008	3
2009	3
2010	14
2011	13
2012	11
2013	13
2014	11
2015	14
2016	10
2017	12
2018	18
2019	13
2020	10
2021	14
2022	13
2023	17
2024	2

1

Anti-factor B antibodies in atypical hemolytic uremic syndrome.

Khandelwal P, Nambiar S, Saini R, Saini S, Coshic P, Sinha A, Hari P, Palanichamy JK, Bagga A. Khandelwal P, et al. Pediatr Nephrol. 2024 Jun;39(6):1909-1916. doi: 10.1007/s00467-024-06284-x. Epub 2024 Jan 22. Pediatr Nephrol. 2024. PMID: 38252289

2

[Various phenotypes of postpartum atypical hemolytic uremic syndrome: the role of genetic testing in determining prognosis. Case report].

Kirsanova TV, Balakireva AI, Fedorova TA, Pyregov AV, Rogachevskiy OV. Kirsanova TV, et al. Ter Arkh. 2023 Aug 17;95(6):511-515. doi: 10.26442/00403660.2023.06.202233. Ter Arkh. 2023. PMID: 38158972 Russian.

3

Complement-mediated thrombotic microangiopathy treated with anticomplement protein 5 therapy, a retrospective study.

Laber DA, Patel PC, Logothetis CN, Patel AK, Jaglal M, Haider M, Visweshwar N, Rajasekaran-Rathnakumar G, Eatrides J. Laber DA, et al. Eur J Haematol. 2024 Mar;112(3):450-457. doi: 10.1111/ejh.14136. Epub 2023 Nov 20. Eur J Haematol. 2024. PMID: 37984551

4

The Rationale of Complement Blockade of the MCP_ggaac Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review.

Turudic D, Pokrajac D, Tasic V, Kasumovic D, Prohaszka Z, Milosevic D. Turudic D, et al. Int J Mol Sci. 2023 Aug 22;24(17):13041. doi: 10.3390/ijms241713041. Int J Mol Sci. 2023. PMID: 37685848 Free PMC article. Review.

5

Complement Factor I Gene Variant in an Atypical Hemolytic Uremic Syndrome Triggered by Hypereosinophilia Syndrome.

Banjongjit A, Kittanamongkolchai W, Kanjanabuch T. Banjongjit A, et al. Nephron. 2023;147(11):701-706. doi: 10.1159/000531879. Epub 2023 Aug 23. Nephron. 2023. PMID: 37611541 Free article.

6

New-onset and relapsed thrombotic microangiopathy post-COVID-19 vaccination.

Ma Q, Xu G. Ma Q, et al. J Med Virol. 2023 Jul;95(7):e28946. doi: 10.1002/jmv.28946. J Med Virol. 2023. PMID: 37436788 Review.

7

Atypical hemolytic uremic syndrome in the era of terminal complement inhibition: an observational cohort study.

Brocklebank V, Walsh PR, Smith-Jackson K, Hallam TM, Marchbank KJ, Wilson V, Bigirumurame T, Dutt T, Montgomery EK, Malina M, Wong EKS, Johnson S, Sheerin NS, Kavanagh D. Brocklebank V, et al. Blood. 2023 Oct 19;142(16):1371-1386. doi: 10.1182/blood.2022018833. Blood. 2023. PMID: 37369098 Free PMC article.

8

Mutations in atypical hemolytic uremic syndrome provide evidence for the role of calcium in complement factor I.

Java A, Atkinson J, Hu Z, Pozzi N. Java A, et al. Blood. 2023 Aug 10;142(6):607-610. doi: 10.1182/blood.2022019361. Blood. 2023. PMID: 37363824

9

Kidney Transplant Outcomes in Patients with Atypical Hemolytic Uremic Syndrome.

Balwani MR, Pasari AS, Gurjar P, Bhawane A, Bawankule C, Tolani P, Kashiv P, Dubey S, Katekhaye VM. Balwani MR, et al. Transplant Proc. 2023 Jun;55(5):1312-1315. doi: 10.1016/j.transproceed.2023.02.066. Epub 2023 May 16. Transplant Proc. 2023. PMID: 37202305

10

Onconephrology and Thrombotic Microangiopathy: Looking Beyond the Horizon.

Gudsoorkar P, Abudayyeh A, Tchakarov A, Hanna R. Gudsoorkar P, et al. Semin Nephrol. 2022 Nov;42(6):151345. doi: 10.1016/j.semnephrol.2023.151345. Epub 2023 May 15. Semin Nephrol. 2022. PMID: 37196461 Review.

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