Results 1 to 10 of about 24,724 (214)
Hemophagocytic lymphohistiocytosis secondary to dengue fever
European Journal of Case Reports in Internal MedicineHemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome often misdiagnosed due to its rarity and overlapping symptoms with sepsis or organ dysfunction.
Simon Kashfi +4 more
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HLH-1 Modulates Muscle Proteostasis During Caenorhabditis elegans Larval Development
Frontiers in Cell and Developmental Biology, 2022 Muscle proteostasis is shaped by the myogenic transcription factor MyoD which regulates the expression of chaperones during muscle differentiation. Whether MyoD can also modulate chaperone expression in terminally differentiated muscle cells remains open.
Khairun Nisaa, Anat Ben-Zvi
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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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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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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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Fatal case of EBV induced hemophagocytic lymphohistiocytosis (HLH), presenting with acute abdomen
Saudi Journal of Emergency MedicineIntroduction : Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome with excessive immune activation. Primary or secondary HLH, have a high mortality rate approaching 50%, despite multiple management regiments.
Gina Rami Salama Ibrahim Abdelmesih
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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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BMC Infectious Diseases, 2021 Background Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive inflammation. We aimed to describe the clinical and laboratory findings of HLH patients secondary to Visceral leishmaniasis (VL) and their treatment outcome during a 4-year ...
Hadi Mottaghipisheh +9 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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Biophysical Properties and Cytotoxicity of Feruloylated Helix Lucorum Hemocyanin
Acta Chimica Slovenica, 2020 For the first time Helix lucorum hemocyanin (HlH) has been feruloylated. Two HlH conjugates with 40- and 120- ferulic acid residues were prepared, denoted as FA-HlH-1 and FA-HlH-2.
Maya Guncheva +4 more
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