Similar articles for PMID: 26597256

Year	Number of Results
2002	1
2003	1
2004	2
2005	4
2006	3
2007	6
2008	2
2009	7
2010	8
2011	13
2012	13
2013	20
2014	9
2015	16
2016	27
2017	28
2018	19
2019	26
2020	33
2021	27
2022	21
2023	7
2024	0

1

Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza.

Schulert GS, Zhang M, Fall N, Husami A, Kissell D, Hanosh A, Zhang K, Davis K, Jentzen JM, Napolitano L, Siddiqui J, Smith LB, Harms PW, Grom AA, Cron RQ. Schulert GS, et al. J Infect Dis. 2016 Apr 1;213(7):1180-8. doi: 10.1093/infdis/jiv550. Epub 2015 Nov 23. J Infect Dis. 2016. PMID: 26597256 Free PMC article.

2

Whole-exome sequencing reveals overlap between macrophage activation syndrome in systemic juvenile idiopathic arthritis and familial hemophagocytic lymphohistiocytosis.

Kaufman KM, Linghu B, Szustakowski JD, Husami A, Yang F, Zhang K, Filipovich AH, Fall N, Harley JB, Nirmala NR, Grom AA. Kaufman KM, et al. Arthritis Rheumatol. 2014 Dec;66(12):3486-95. doi: 10.1002/art.38793. Arthritis Rheumatol. 2014. PMID: 25047945 Free PMC article.

3

The genetics of macrophage activation syndrome.

Schulert GS, Cron RQ. Schulert GS, et al. Genes Immun. 2020 May;21(3):169-181. doi: 10.1038/s41435-020-0098-4. Epub 2020 Apr 15. Genes Immun. 2020. PMID: 32291394 Review.

4

Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis.

Mukda E, Trachoo O, Pasomsub E, Tiyasirichokchai R, Iemwimangsa N, Sosothikul D, Chantratita W, Pakakasama S. Mukda E, et al. Int J Hematol. 2017 Aug;106(2):282-290. doi: 10.1007/s12185-017-2223-3. Epub 2017 Mar 28. Int J Hematol. 2017. PMID: 28353193

5

A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis.

Bordbar MR, Modarresi F, Farazi Fard MA, Dastsooz H, Shakib Azad N, Faghihi MA. Bordbar MR, et al. BMC Med Genet. 2017 May 3;18(1):49. doi: 10.1186/s12881-017-0404-9. BMC Med Genet. 2017. PMID: 28468610 Free PMC article.

6

Hemophagocytic Lymphohistiocytosis Gene Variants in Childhood-Onset Systemic Lupus Erythematosus With Macrophage Activation Syndrome.

Lahiry P, Naumenko S, Couse M, Liao F, Dominguez D, Knight A, Levy DM, Misztal M, Ng LWK, Hiraki LT. Lahiry P, et al. J Rheumatol. 2022 Oct;49(10):1146-1151. doi: 10.3899/jrheum.211200. Epub 2022 Jun 1. J Rheumatol. 2022. PMID: 35649546

7

Mutations of the hemophagocytic lymphohistiocytosis-associated gene UNC13D in a patient with systemic juvenile idiopathic arthritis.

Hazen MM, Woodward AL, Hofmann I, Degar BA, Grom A, Filipovich AH, Binstadt BA. Hazen MM, et al. Arthritis Rheum. 2008 Feb;58(2):567-70. doi: 10.1002/art.23199. Arthritis Rheum. 2008. PMID: 18240215 Free article.

8

Cytokine Storm Syndrome.

Cron RQ, Goyal G, Chatham WW. Cron RQ, et al. Annu Rev Med. 2023 Jan 27;74:321-337. doi: 10.1146/annurev-med-042921-112837. Epub 2022 Oct 13. Annu Rev Med. 2023. PMID: 36228171 Free article. Review.

9

Clinico-laboratory profile and perforin gene mutations of pediatric hemophagocytic lymphohistiocytosis cases: a five-year single center study.

Almalky MA, Saleh SHA, Baz EG, Fakhr AE. Almalky MA, et al. Pan Afr Med J. 2020 Aug 27;36:354. doi: 10.11604/pamj.2020.36.354.25079. eCollection 2020. Pan Afr Med J. 2020. PMID: 33224420 Free PMC article.

10

Hemophagocytic lymphohistiocytosis: when the immune system runs amok.

Janka G. Janka G. Klin Padiatr. 2009 Sep;221(5):278-85. doi: 10.1055/s-0029-1237386. Epub 2009 Aug 25. Klin Padiatr. 2009. PMID: 19707989 Review.

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