340 related articles for article (PubMed ID: 25086802)
1. Genetic defects in cytolysis in macrophage activation syndrome.
Zhang M; Behrens EM; Atkinson TP; Shakoory B; Grom AA; Cron RQ
Curr Rheumatol Rep; 2014; 16(9):439. PubMed ID: 25086802
[TBL] [Abstract][Full Text] [Related]
2. The genetics of macrophage activation syndrome.
Schulert GS; Cron RQ
Genes Immun; 2020 May; 21(3):169-181. PubMed ID: 32291394
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Natural Killer Cells in Systemic Autoinflammatory Diseases: A Focus on Systemic Juvenile Idiopathic Arthritis and Macrophage Activation Syndrome.
Vandenhaute J; Wouters CH; Matthys P
Front Immunol; 2019; 10():3089. PubMed ID: 32010140
[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. The Immunology of Macrophage Activation Syndrome.
Crayne CB; Albeituni S; Nichols KE; Cron RQ
Front Immunol; 2019; 10():119. PubMed ID: 30774631
[TBL] [Abstract][Full Text] [Related]
7. 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
Arthritis Rheumatol; 2014 Dec; 66(12):3486-95. PubMed ID: 25047945
[TBL] [Abstract][Full Text] [Related]
8. Cytokine Storm Syndrome.
Cron RQ; Goyal G; Chatham WW
Annu Rev Med; 2023 Jan; 74():321-337. PubMed ID: 36228171
[TBL] [Abstract][Full Text] [Related]
9. Mutations in the perforin gene can be linked to macrophage activation syndrome in patients with systemic onset juvenile idiopathic arthritis.
Vastert SJ; van Wijk R; D'Urbano LE; de Vooght KM; de Jager W; Ravelli A; Magni-Manzoni S; Insalaco A; Cortis E; van Solinge WW; Prakken BJ; Wulffraat NM; de Benedetti F; Kuis W
Rheumatology (Oxford); 2010 Mar; 49(3):441-9. PubMed ID: 20019066
[TBL] [Abstract][Full Text] [Related]
10. Clinical features and correct diagnosis of macrophage activation syndrome.
Cron RQ; Davi S; Minoia F; Ravelli A
Expert Rev Clin Immunol; 2015; 11(9):1043-53. PubMed ID: 26082353
[TBL] [Abstract][Full Text] [Related]
11. Macrophage activation syndrome as part of systemic juvenile idiopathic arthritis: diagnosis, genetics, pathophysiology and treatment.
Ravelli A; Grom AA; Behrens EM; Cron RQ
Genes Immun; 2012 Jun; 13(4):289-98. PubMed ID: 22418018
[TBL] [Abstract][Full Text] [Related]
12. Interleukin-18 diagnostically distinguishes and pathogenically promotes human and murine macrophage activation syndrome.
Weiss ES; Girard-Guyonvarc'h C; Holzinger D; de Jesus AA; Tariq Z; Picarsic J; Schiffrin EJ; Foell D; Grom AA; Ammann S; Ehl S; Hoshino T; Goldbach-Mansky R; Gabay C; Canna SW
Blood; 2018 Mar; 131(13):1442-1455. PubMed ID: 29326099
[TBL] [Abstract][Full Text] [Related]
13. Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia.
Esmaeilzadeh H; Bemanian MH; Nabavi M; Arshi S; Fallahpour M; Fuchs I; zur Stadt U; Warnatz K; Ammann S; Ehl S; Lehmberg K; Rezaei N
J Clin Immunol; 2015 Jan; 35(1):22-5. PubMed ID: 25491289
[TBL] [Abstract][Full Text] [Related]
14. Macrophage activation syndrome in autoimmune disease.
Deane S; Selmi C; Teuber SS; Gershwin ME
Int Arch Allergy Immunol; 2010; 153(2):109-20. PubMed ID: 20407267
[TBL] [Abstract][Full Text] [Related]
15. 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
J Infect Dis; 2016 Apr; 213(7):1180-8. PubMed ID: 26597256
[TBL] [Abstract][Full Text] [Related]
16. Familial hemophagocytic lymphohistiocytosis: a model for understanding the human machinery of cellular cytotoxicity.
Sieni E; Cetica V; Mastrodicasa E; Pende D; Moretta L; Griffiths G; Aricò M
Cell Mol Life Sci; 2012 Jan; 69(1):29-40. PubMed ID: 21990010
[TBL] [Abstract][Full Text] [Related]
17. Macrophage activation syndrome and cytokine-directed therapies.
Schulert GS; Grom AA
Best Pract Res Clin Rheumatol; 2014 Apr; 28(2):277-92. PubMed ID: 24974063
[TBL] [Abstract][Full Text] [Related]
18. Efficacy of Moderately Dosed Etoposide in Macrophage Activation Syndrome-Hemophagocytic Lymphohistiocytosis.
Horne A; von Bahr Greenwood T; Chiang SCC; Meeths M; Björklund C; Ekelund M; Erensjö P; Berg S; Hagelberg S; Bryceson YT; Andersson U; Henter JI
J Rheumatol; 2021 Oct; 48(10):1596-1602. PubMed ID: 33589555
[TBL] [Abstract][Full Text] [Related]
19. Genetic Deficiency of Interferon-γ Reveals Interferon-γ-Independent Manifestations of Murine Hemophagocytic Lymphohistiocytosis.
Burn TN; Weaver L; Rood JE; Chu N; Bodansky A; Kreiger PA; Behrens EM
Arthritis Rheumatol; 2020 Feb; 72(2):335-347. PubMed ID: 31400073
[TBL] [Abstract][Full Text] [Related]
20. 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
Arthritis Rheum; 2008 Feb; 58(2):567-70. PubMed ID: 18240215
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]