163 related articles for article (PubMed ID: 30782130)
1. Novel mutations of STXBP2 and LYST associated with adult haemophagocytic lymphohistiocytosis with Epstein-Barr virus infection: a case report.
Sheng L; Zhang W; Gu J; Shen K; Luo H; Yang Y
BMC Med Genet; 2019 Feb; 20(1):34. PubMed ID: 30782130
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of the novel L243R mutation in STXBP2 reveals impairment of degranulation activity.
Viñas-Giménez L; Donadeu L; Alsina L; Rincón R; de la Campa EÁ; Esteve-Sole A; Català A; Colobran R; de la Cruz X; Sayós J; Martínez-Gallo M
Int J Hematol; 2020 Mar; 111(3):440-450. PubMed ID: 31865540
[TBL] [Abstract][Full Text] [Related]
3. Clinical presentation and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in China: A retrospective multicenter study.
Xu XJ; Wang HS; Ju XL; Xiao PF; Xiao Y; Xue HM; Shi HY; Gao YJ; Jia GC; Li XR; Zhao WH; Wang NL; Tang YM;
Pediatr Blood Cancer; 2017 Apr; 64(4):. PubMed ID: 27781387
[TBL] [Abstract][Full Text] [Related]
4. [The study of gene mutations in unknown refractory viral infection and primary hemophagocytic lymphohistiocytosis].
Tong CR; Liu HX; Xie JJ; Wang F; Cai P; Wang H; Zhu J; Teng W; Zhang X; Yang JF; Zhang YL; Fei XH; Zhao J; Yin YM; Wu T; Wang JB; Sun Y; Liu R; Shi XD; Lu DP
Zhonghua Nei Ke Za Zhi; 2011 Apr; 50(4):280-3. PubMed ID: 21600143
[TBL] [Abstract][Full Text] [Related]
5. 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]
6.
Benavides N; Spessott WA; Sanmillan ML; Vargas M; Livingston MS; Erickson N; Pozos TC; McCormick ME; Scharrig E; Messinger YH; Giraudo CG
Front Immunol; 2020; 11():545414. PubMed ID: 33162974
[TBL] [Abstract][Full Text] [Related]
7. Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient With Hemophagocytic Syndrome and Langerhans Cell Histiocytosis.
Viñas-Giménez L; Rincón R; Colobran R; de la Cruz X; Celis VP; Dapena JL; Alsina L; Sayós J; Martínez-Gallo M
Front Immunol; 2021; 12():723836. PubMed ID: 34630398
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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
Int J Hematol; 2017 Aug; 106(2):282-290. PubMed ID: 28353193
[TBL] [Abstract][Full Text] [Related]
10. STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5.
Cetica V; Santoro A; Gilmour KC; Sieni E; Beutel K; Pende D; Marcenaro S; Koch F; Grieve S; Wheeler R; Zhao F; zur Stadt U; Griffiths GM; Aricò M
J Med Genet; 2010 Sep; 47(9):595-600. PubMed ID: 20798128
[TBL] [Abstract][Full Text] [Related]
11. Haemophagocytic lymphohistiocytosis and Epstein-Barr virus: a complex relationship with diverse origins, expression and outcomes.
El-Mallawany NK; Curry CV; Allen CE
Br J Haematol; 2022 Jan; 196(1):31-44. PubMed ID: 34169507
[TBL] [Abstract][Full Text] [Related]
12. Familial hemophagocytic lymphohistiocytosis type 5 in a Chinese Tibetan patient caused by a novel compound heterozygous mutation in STXBP2.
Tang X; Guo X; Li Q; Huang Z
Medicine (Baltimore); 2019 Oct; 98(43):e17674. PubMed ID: 31651895
[TBL] [Abstract][Full Text] [Related]
13. Epstein-Barr virus-associated haemophagocytic lymphohistiocytosis complicated by neurological involvement in a patient with dermatomyositis: A case report and literature review.
Xu T; Xiong L; Tang L
Mod Rheumatol Case Rep; 2023 Jan; 7(1):293-297. PubMed ID: 35861298
[TBL] [Abstract][Full Text] [Related]
14. Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation.
Albayrak M; Kaya Z; Yilmaz-Keskin E; Stadt UZ; Koçak U; Gürsel T
Turk J Pediatr; 2009; 51(4):371-4. PubMed ID: 19950846
[TBL] [Abstract][Full Text] [Related]
15. Secondary Leukemia in a Patient With EBV-HLH Carrying Heterozygous STXBP2 Variant.
Liao M; Yu J
J Pediatr Hematol Oncol; 2022 Mar; 44(2):e526-e528. PubMed ID: 33661178
[TBL] [Abstract][Full Text] [Related]
16. Hemophagocytic lymphohistiocytosis caused by dominant-negative mutations in STXBP2 that inhibit SNARE-mediated membrane fusion.
Spessott WA; Sanmillan ML; McCormick ME; Patel N; Villanueva J; Zhang K; Nichols KE; Giraudo CG
Blood; 2015 Mar; 125(10):1566-77. PubMed ID: 25564401
[TBL] [Abstract][Full Text] [Related]
17. Treatment of Epstein Barr virus-induced haemophagocytic lymphohistiocytosis with rituximab-containing chemo-immunotherapeutic regimens.
Chellapandian D; Das R; Zelley K; Wiener SJ; Zhao H; Teachey DT; Nichols KE;
Br J Haematol; 2013 Aug; 162(3):376-82. PubMed ID: 23692048
[TBL] [Abstract][Full Text] [Related]
18. Severe hemorrhagic coagulopathy with hemophagocytic lymphohistiocytosis secondary to Epstein-Barr virus-associated T-cell lymphoproliferative disorder.
Nawathe PA; Ravindranath TM; Satwani P; Baird JS
Pediatr Crit Care Med; 2013 May; 14(4):e176-81. PubMed ID: 23439459
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Pediatric hemophagocytic lymphohistiocytosis.
Canna SW; Marsh RA
Blood; 2020 Apr; 135(16):1332-1343. PubMed ID: 32107531
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]