307 related articles for article (PubMed ID: 32375849)
1. Genotype characteristics and immunological indicator evaluation of 311 hemophagocytic lymphohistiocytosis cases in China.
Zhang J; Sun Y; Shi X; Zhang R; Wang Y; Xiao J; Cao J; Gao Z; Wang J; Wu L; Wei W; Wang Z
Orphanet J Rare Dis; 2020 May; 15(1):112. PubMed ID: 32375849
[TBL] [Abstract][Full Text] [Related]
2. [Evaluation of CD107a and perforin expression detection in the diagnosis of primary hemophagocytic lymphohistiocytosis].
Zhang J; Sun Y; Zhang R; Xiao J; Wang JS; Wu L; Song Y; Wang Z
Zhonghua Yi Xue Za Zhi; 2022 Jul; 102(28):2161-2166. PubMed ID: 35872579
[No Abstract] [Full Text] [Related]
3. Genetic and clinical characteristics of primary hemophagocytic lymphohistiocytosis in children.
Zhao C; Zhang Q; Zhang R; Lian H; Ma H; Zhao X; Li Z
Ann Hematol; 2024 Jan; 103(1):17-28. PubMed ID: 37851074
[TBL] [Abstract][Full Text] [Related]
4. Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH.
Rubin TS; Zhang K; Gifford C; Lane A; Choo S; Bleesing JJ; Marsh RA
Blood; 2017 Jun; 129(22):2993-2999. PubMed ID: 28270454
[TBL] [Abstract][Full Text] [Related]
5. [The significance of pedigree genetic screening and rapid immunological parameters in the diagnosis of primary hemophagocytic lymphohistiocytosis].
Zhang J; Wang YN; Wang JS; Wu L; Wei N; Fu L; Gao Z; Chen JH; Pei RJ; Wang Z
Zhonghua Xue Ye Xue Za Zhi; 2016 Jul; 37(7):565-70. PubMed ID: 27535855
[TBL] [Abstract][Full Text] [Related]
6. Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.
Zhizhuo H; Junmei X; Yuelin S; Qiang Q; Chunyan L; Zhengde X; Kunling S
Pediatr Blood Cancer; 2012 Mar; 58(3):410-4. PubMed ID: 21674762
[TBL] [Abstract][Full Text] [Related]
7. Genetic characterization of pediatric primary hemophagocytic lymphohistiocytosis in China: a single-center study.
Zhang L; Li Z; Liu W; Ma H; Wang T; Zhang R
Ann Hematol; 2019 Oct; 98(10):2303-2310. PubMed ID: 31388699
[TBL] [Abstract][Full Text] [Related]
8. Genetic variant spectrum in 265 Chinese patients with hemophagocytic lymphohistiocytosis: Molecular analyses of PRF1, UNC13D, STX11, STXBP2, SH2D1A, and XIAP.
Chen X; Wang F; Zhang Y; Teng W; Wang M; Nie D; Zhou X; Wang D; Zhao H; Zhu P; Liu H
Clin Genet; 2018 Aug; 94(2):200-212. PubMed ID: 29665027
[TBL] [Abstract][Full Text] [Related]
9. Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis.
Xinh PT; Chuong HQ; Diem TPH; Nguyen TM; Van ND; Mai Anh NH; Nghia H; Vu HA
Int J Lab Hematol; 2021 Dec; 43(6):1524-1530. PubMed ID: 34339548
[TBL] [Abstract][Full Text] [Related]
10. A Rare STXBP2 Mutation in Severe COVID-19 and Secondary Cytokine Storm Syndrome.
Reiff DD; Zhang M; Smitherman EA; Mannion ML; Stoll ML; Weiser P; Cron RQ
Life (Basel); 2022 Jan; 12(2):. PubMed ID: 35207437
[TBL] [Abstract][Full Text] [Related]
11. Primary hemophagocytic lymphohistiocytosis in adults: the utility of family surveys in a single-center study from China.
Jin Z; Wang Y; Wang J; Zhang J; Wu L; Gao Z; Lai W; Wang Z
Orphanet J Rare Dis; 2018 Jan; 13(1):17. PubMed ID: 29357941
[TBL] [Abstract][Full Text] [Related]
12. The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India.
Shabrish S; Kelkar M; Yadav RM; Bargir UA; Gupta M; Dalvi A; Aluri J; Kulkarni M; Shinde S; Sawant-Desai S; Kambli P; Hule G; Setia P; Jodhawat N; Gaikwad P; Dhawale A; Nambiar N; Gowri V; Pandrowala A; Taur P; Raj R; Uppuluri R; Sharma R; Kini P; Sivasankaran M; Munirathnam D; Vedam R; Vignesh P; Banday A; Rawat A; Aggarwal A; Poddar U; Girish M; Chaudhary A; Sampagar A; Jayaraman D; Chaudhary N; Shah N; Jijina F; Chandrakla S; Kanakia S; Arora B; Sen S; Lokeshwar M; Desai M; Madkaikar M
Front Immunol; 2021; 12():612583. PubMed ID: 33746956
[TBL] [Abstract][Full Text] [Related]
13. Application of blood and immunodeficiency gene detection in the diagnosis of hemophagocytic lymphohistiocytosis patients.
Mo W; Wei W; Sun Y; Yang Y; Guan Z; Li M; Zhu P; Chi Z
Exp Hematol; 2019 Oct; 78():62-69. PubMed ID: 31562900
[TBL] [Abstract][Full Text] [Related]
14. Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases.
Rohr J; Beutel K; Maul-Pavicic A; Vraetz T; Thiel J; Warnatz K; Bondzio I; Gross-Wieltsch U; Schündeln M; Schütz B; Woessmann W; Groll AH; Strahm B; Pagel J; Speckmann C; Janka G; Griffiths G; Schwarz K; zur Stadt U; Ehl S
Haematologica; 2010 Dec; 95(12):2080-7. PubMed ID: 20823128
[TBL] [Abstract][Full Text] [Related]
15. [Clinical and genetic mutation characteristics of patients with primary hemophagocytic lymphohistiocytosis and their impact on prognosis].
Dou LR; Yu MZ; Shi L; Zhang J; Wu L; Wang JS; Wang Z
Zhonghua Yi Xue Za Zhi; 2024 Jun; 104(23):2160-2166. PubMed ID: 38871474
[No Abstract] [Full Text] [Related]
16. Subtypes of familial hemophagocytic lymphohistiocytosis in Japan based on genetic and functional analyses of cytotoxic T lymphocytes.
Nagai K; Yamamoto K; Fujiwara H; An J; Ochi T; Suemori K; Yasumi T; Tauchi H; Koh K; Sato M; Morimoto A; Heike T; Ishii E; Yasukawa M
PLoS One; 2010 Nov; 5(11):e14173. PubMed ID: 21152410
[TBL] [Abstract][Full Text] [Related]
17. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
Zur Stadt U; Beutel K; Kolberg S; Schneppenheim R; Kabisch H; Janka G; Hennies HC
Hum Mutat; 2006 Jan; 27(1):62-8. PubMed ID: 16278825
[TBL] [Abstract][Full Text] [Related]
18. A CD57
Hori M; Yasumi T; Shimodera S; Shibata H; Hiejima E; Oda H; Izawa K; Kawai T; Ishimura M; Nakano N; Shirakawa R; Nishikomori R; Takada H; Morita S; Horiuchi H; Ohara O; Ishii E; Heike T
J Clin Immunol; 2017 Jan; 37(1):92-99. PubMed ID: 27896523
[TBL] [Abstract][Full Text] [Related]
19. 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
Haematologica; 2010 Apr; 95(4):622-6. PubMed ID: 20015888
[TBL] [Abstract][Full Text] [Related]
20. A cell-based functional assay that accurately links genotype to phenotype in familial HLH.
Noori T; Rudd-Schmidt JA; Kane A; Frith K; Gray PE; Hu H; Hsu D; Chung CWT; Hodel AW; Trapani JA; Voskoboinik I
Blood; 2023 May; 141(19):2330-2342. PubMed ID: 36706356
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
