These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
10. Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity. Meeths M; Chiang SC; Löfstedt A; Müller ML; Tesi B; Henter JI; Bryceson YT Exp Cell Res; 2014 Jul; 325(1):10-7. PubMed ID: 24680986 [TBL] [Abstract][Full Text] [Related]
11. Mouse Cytomegalovirus Infection in BALB/c Mice Resembles Virus-Associated Secondary Hemophagocytic Lymphohistiocytosis and Shows a Pathogenesis Distinct from Primary Hemophagocytic Lymphohistiocytosis. Brisse E; Imbrechts M; Put K; Avau A; Mitera T; Berghmans N; Rutgeerts O; Waer M; Ninivaggi M; Kelchtermans H; Boon L; Snoeck R; Wouters CH; Andrei G; Matthys P J Immunol; 2016 Apr; 196(7):3124-34. PubMed ID: 26903481 [TBL] [Abstract][Full Text] [Related]
12. An animal model of hemophagocytic lymphohistiocytosis (HLH): CD8+ T cells and interferon gamma are essential for the disorder. Jordan MB; Hildeman D; Kappler J; Marrack P Blood; 2004 Aug; 104(3):735-43. PubMed ID: 15069016 [TBL] [Abstract][Full Text] [Related]
17. Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome. Villanueva J; Lee S; Giannini EH; Graham TB; Passo MH; Filipovich A; Grom AA Arthritis Res Ther; 2005; 7(1):R30-7. PubMed ID: 15642140 [TBL] [Abstract][Full Text] [Related]
18. Functional and genetic testing in adults with HLH reveals an inflammatory profile rather than a cytotoxicity defect. Carvelli J; Piperoglou C; Farnarier C; Vely F; Mazodier K; Audonnet S; Nitschke P; Bole-Feysot C; Boucekine M; Cambon A; Hamidou M; Harle JR; de Saint Basile G; Kaplanski G Blood; 2020 Jul; 136(5):542-552. PubMed ID: 32356861 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]