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

Year Number of Results
2006 3
2007 1
2008 2
2009 6
2010 9
2011 6
2012 7
2013 5
2014 14
2015 13
2016 14
2017 13
2018 10
2019 13
2020 11
2021 1
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Similar articles for PMID: 31261095

114 results
Results by year
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Neonatal Hemophagocytic Lymphohistiocytosis.
McLean J, Katebian R, Suh E, Mirza K, Amin S. McLean J, et al. Neoreviews. 2019 Jun;20(6):e316-e325. doi: 10.1542/neo.20-6-e316. Neoreviews. 2019. PMID: 31261095 Review.
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.
Tesi B, Lagerstedt-Robinson K, Chiang SC, Ben Bdira E, Abboud M, Belen B, Devecioglu O, Fadoo Z, Yeoh AE, Erichsen HC, Möttönen M, Akar HH, Hästbacka J, Kaya Z, Nunes S, Patiroglu T, Sabel M, Saribeyoglu ET, Tvedt TH, Unal E, Unal S, Unuvar A, Meeths M, Henter JI, Nordenskjöld M, Bryceson YT. Tesi B, et al. Genome Med. 2015 Dec 18;7:130. doi: 10.1186/s13073-015-0244-1. Genome Med. 2015. PMID: 26684649 Free PMC article.
UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis.
Yoon HS, Kim HJ, Yoo KH, Sung KW, Koo HH, Kang HJ, Shin HY, Ahn HS, Kim JY, Lim YT, Bae KW, Lee KO, Shin JS, Lee ST, Chung HS, Kim SH, Park CJ, Chi HS, Im HJ, Seo JJ. Yoon HS, et al. Haematologica. 2010 Apr;95(4):622-6. doi: 10.3324/haematol.2009.016949. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015888 Free PMC article.
Clinical features, genetics, and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in Korea: report of a nationwide survey from Korea Histiocytosis Working Party.
Koh KN, Im HJ, Chung NG, Cho B, Kang HJ, Shin HY, Lyu CJ, Yoo KH, Koo HH, Kim HJ, Baek HJ, Kook H, Yoon HS, Lim YT, Kim HS, Ryu KH, Seo JJ; Korea Histiocytosis Working Party. Koh KN, et al. Eur J Haematol. 2015 Jan;94(1):51-9. doi: 10.1111/ejh.12399. Epub 2014 Jul 3. Eur J Haematol. 2015. PMID: 24935083 Free PMC article.
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