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Indian Journal of Pathology and Microbiology, 2021 Hemophagocytic lymphohistiocytosis (HLH) is a rare and potentially life-threatening condition associated with high mortality and can be classified into primary (familial) and secondary HLH.
Subramaniam Ramkumar
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HLH-1 is required for establishing muscle proteostasis.
, 2016 (A) Q0, Q35, Q0;hlh-1(cc561) or Q35;hlh-1(cc561) embryos laid at 15°C were scored for embryonic arrest. Data are presented as means ± SEM of at least 6 independent experiments.
Yael Bar-Lavan (3608987) +5 more
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Dengue hemorhagic fever associated hemophagocytc lymphohistiocytosis in primigravida: A case report
Asian Pacific Journal of Tropical MedicineRationale: Hemophagocytic lymphohistiocytosis (HLH) is a rare but severe complication of dengue virus infection, associated with high mortality. We report a case of a 9-week primigravida presenting with high grade fever spikes and a positive Dengue NS1 ...
Pyrus Bhellum +3 more
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Frontiers in Immunology, 2019 Hemophagocytic lymphohistiocytosis (HLH) can be classified into primary HLH and secondary HLH. Primary HLH usually occurs in infants and children with an underlying genetic defect, and there are also teens and occasional adults with primary HLH.
Yi Miao +47 more
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Genetic features of late onset primary hemophagocytic lymphohistiocytosis in adolescence or adulthood. [PDF]
PLoS ONE, 2014 Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening condition of uncontrolled immune activation leading to extreme inflammation. Primary HLH was once believed to be a disease that occurred only in infancy or young children, and was rarely ...
Yini Wang +9 more
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, 2019 In wild-type C. elegans under starvation conditions, HLH-30 activates lysosome biogenesis and catabolic pathways, which encourage starvation survival and prime the animal for recovery from starvation upon re-feeding. Without HLH-30, C.
Ben Zhou (197219) +1 more
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Mediterranean Journal of Hematology and Infectious Diseases, 2014 Background and objective: Hemophagocytic lymphohistiocytosis (HLH) is a life threatening hyper inflammatory disease. It is difficult to differentiate between primary and secondary HLH based on clinical findings at the onset of disease.
seval ozen +7 more
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Extreme hypertriglyceridemia in an infant with hemophagocytic lymphohistiocytosis and hydroxycobalamin deficiency [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2015 Introduction. Hemophagocytic lymphohistiocytosis (HLH) is a severe hyperinflammatory condition characterized by fever, cytopenias, hepatosplenomegaly and hemophagocytosis.
Dokmanović Lidija +6 more
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Frontiers in Oncology, 2023 Haemophagocytic lymphohistiocytosis (HLH) is a cytokine-driven inflammatory syndrome caused by uncontrolled hypersecretion of inflammatory cytokines. Conventional first-line treatment for HLH included HLH-94 and HLH-2004 regimens.
Lin Zhao +4 more
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HLHS: Power of the Chick Model
Journal of Cardiovascular Development and Disease, 2022 Background: Hypoplastic left heart syndrome (HLHS) is a rare but deadly form of human congenital heart disease, most likely of diverse etiologies. Hemodynamic alterations such as those resulting from premature foramen ovale closure or aortic stenosis are among the possible pathways.
openaire +3 more sources