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6,773 results

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Page 1
HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.
Henter JI, Horne A, Aricó M, Egeler RM, Filipovich AH, Imashuku S, Ladisch S, McClain K, Webb D, Winiarski J, Janka G. Henter JI, et al. Pediatr Blood Cancer. 2007 Feb;48(2):124-31. doi: 10.1002/pbc.21039. Pediatr Blood Cancer. 2007. PMID: 16937360
In HLH-94, the first prospective international treatment study for hemophagocytic lymphohistiocytosis (HLH), diagnosis was based on five criteria (fever, splenomegaly, bicytopenia, hypertriglyceridemia and/or hypofibrinogenemia, and hemophagocytosis). ...
In HLH-94, the first prospective international treatment study for hemophagocytic lymphohistiocytosis (HLH), diagnosis was bas …
Approaching hemophagocytic lymphohistiocytosis.
Chinnici A, Beneforti L, Pegoraro F, Trambusti I, Tondo A, Favre C, Coniglio ML, Sieni E. Chinnici A, et al. Front Immunol. 2023 Jun 22;14:1210041. doi: 10.3389/fimmu.2023.1210041. eCollection 2023. Front Immunol. 2023. PMID: 37426667 Free PMC article. Review.
Hemophagocytic Lymphohistiocytosis (HLH) is a rare clinical condition characterized by sustained but ineffective immune system activation, leading to severe and systemic hyperinflammation. ...Genetic analysis is mandatory to confirm familial hemophagocytic
Hemophagocytic Lymphohistiocytosis (HLH) is a rare clinical condition characterized by sustained but ineffective immune system
Hemophagocytic lymphohistiocytosis: An update on pathogenesis, diagnosis, and therapy.
Griffin G, Shenoi S, Hughes GC. Griffin G, et al. Best Pract Res Clin Rheumatol. 2020 Aug;34(4):101515. doi: 10.1016/j.berh.2020.101515. Epub 2020 May 7. Best Pract Res Clin Rheumatol. 2020. PMID: 32387063 Review.
Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening state of immune hyperactivation that arises in the setting of genetic mutations and infectious, inflammatory, or neoplastic triggers. ...
Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening state of immune hyperactivation that arises in the settin
Hemophagocytic Lymphohistiocytosis.
Al-Samkari H, Berliner N. Al-Samkari H, et al. Annu Rev Pathol. 2018 Jan 24;13:27-49. doi: 10.1146/annurev-pathol-020117-043625. Epub 2017 Sep 13. Annu Rev Pathol. 2018. PMID: 28934563 Review.
Hemophagocytic lymphohistiocytosis is a life-threatening disorder characterized by unbridled activation of cytotoxic T lymphocytes, natural killer (NK) cells, and macrophages resulting in hypercytokinemia and immune-mediated injury of multiple organ systems. ...
Hemophagocytic lymphohistiocytosis is a life-threatening disorder characterized by unbridled activation of cytotoxic T lymphoc
Hemophagocytic Lymphohistiocytosis.
Ponnatt TS, Lilley CM, Mirza KM. Ponnatt TS, et al. Arch Pathol Lab Med. 2022 Apr 1;146(4):507-519. doi: 10.5858/arpa.2020-0802-RA. Arch Pathol Lab Med. 2022. PMID: 34347856 Free article. Review.
CONTEXT.-: Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening disorder of immune regulation that can eventually result in end-organ damage and death. ...
CONTEXT.-: Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening disorder of immune regulation that can eventua …
Hemophagocytic Lymphohistiocytosis.
Skinner J, Yankey B, Shelton BK. Skinner J, et al. AACN Adv Crit Care. 2019 Summer;30(2):151-164. doi: 10.4037/aacnacc2019463. AACN Adv Crit Care. 2019. PMID: 31151946 Review.
Hemophagocytic lymphohistiocytosis is a life-threatening condition associated with hyperinflammation and multiple organ dysfunction. ...
Hemophagocytic lymphohistiocytosis is a life-threatening condition associated with hyperinflammation and multiple organ dysfun
History of Hemophagocytic Lymphohistiocytosis.
Janka GE. Janka GE. Adv Exp Med Biol. 2024;1448:9-19. doi: 10.1007/978-3-031-59815-9_2. Adv Exp Med Biol. 2024. PMID: 39117804 Review.
Hemophagocytic lymphohistiocytosis (HLH) is a severe cytokine storm syndrome (CSS), which until the turn of the century, was barely known but is now receiving increased attention. ...
Hemophagocytic lymphohistiocytosis (HLH) is a severe cytokine storm syndrome (CSS), which until the turn of the century, was b
How I treat hemophagocytic lymphohistiocytosis.
Jordan MB, Allen CE, Weitzman S, Filipovich AH, McClain KL. Jordan MB, et al. Blood. 2011 Oct 13;118(15):4041-52. doi: 10.1182/blood-2011-03-278127. Epub 2011 Aug 9. Blood. 2011. PMID: 21828139 Free PMC article. Review.
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation, occurring as either a familial disorder or a sporadic condition, in association with a variety of triggers. ...
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation, occurring as either a familial disorde
Virus-triggered secondary hemophagocytic lymphohistiocytosis.
Imashuku S, Morimoto A, Ishii E. Imashuku S, et al. Acta Paediatr. 2021 Oct;110(10):2729-2736. doi: 10.1111/apa.15973. Epub 2021 Jun 22. Acta Paediatr. 2021. PMID: 34096649 Review.
Primary (familial/hereditary) and secondary (non-familial/hereditary) hemophagocytic lymphohistiocytosis (HLH) are hyperinflammatory and hypercytokinemic syndromes. ...
Primary (familial/hereditary) and secondary (non-familial/hereditary) hemophagocytic lymphohistiocytosis (HLH) are hyperinflam …
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.
Hemophagocytic lymphohistiocytosis (HLH) is extremely rare in the neonatal period. The incidence of neonatal HLH is not confirmed and may range from 1 in 50,000 to 150,000. ...
Hemophagocytic lymphohistiocytosis (HLH) is extremely rare in the neonatal period. The incidence of neonatal HLH is not confir
6,773 results