Results 91 to 100 of about 24,724 (214)
: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome. Complement component 3 (C3), a central effector molecule in 3 separate complement pathways, has been linked to inflammatory diseases.
Xuemei Shu +6 more
doaj +1 more source
HLH-29 Regulates ftn-1 Expression.
(A) Schematic representation of the ftn-1 transgenes used in this study. Empty triangle, predicted HLH-30 binding site (CACGTG); filled triangle, predicted HLH-29 binding sites (CATGCG or CACGCG) with arrows indicating the corresponding orientations ...
Gaolin Zheng Milledge (393588) +4 more
core +1 more source
Effect of PRC1 mutants on HLH-3 protein levels.
Quantification of the fluorescence levels (arbitrary units) in AIY neurons of HLH-3 protein (hlh-3endo::mNeonGreen (vlc28)) at epidermal enclosure embryonic stage. Each dot represents one neuron.
Carole Couillault (271357) +4 more
core +1 more source
Metagenomic analysis of Rhipicephalus linnaei from the Brazilian Amazon revealed the presence of RNA viruses belonging to the families Chuviridae, Phenuiviridae, Orthomyxoviridae and Rhabdoviridae. This study reports the first detection of Brown dog tick mivirus 1 and Brown dog tick phlebovirus 2 in Brazil, based on genomic characterization and ...
Lucas Henrique da Silva e Silva +13 more
wiley +1 more source
ABSTRACT Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare life‐threatening mucocutaneous reactions that remain poorly characterized in pediatric populations. Using the Healthcare Cost and Utilization Project (HCUP) Kids' Inpatient Database (KID), the prevalence of SJS/TEN hospitalizations declined from 0.02% in 2016 to 0.009%
Shazli Razi +5 more
wiley +1 more source
Average temperature as a marker of lymphoma-associated HLH [PDF]
Methods: This retrospective analysis aimed to assess whether a 12-hour mean temperature (measured around either diagnosis of HLH or peak ferritin value) has value as a quick and simple diagnostic test for HLH in people with lymphoproliferative disease ...
Goddard, J. +3 more
core +1 more source
Clinicogenetic Characterization of H Syndrome in a South African Child
ABSTRACT H syndrome is a rare autosomal recessive genodermatosis caused by loss‐of‐function SLC29A3 variants, combining hyperpigmented indurated plaques and hypertrichosis with life‐threatening autoinflammation. We report a 5‐year‐old South African girl of first‐cousin parents who presented with hyperinflammation mimicking macrophage activation ...
Tshimogo Tswelopele Sathekge +1 more
wiley +1 more source
Inherited Hemophagocytic Lymphohistiocytosis (HLH)
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal immune disorder characterized by uncontrolled lymphocyte- and macrophage-activation.
Pachlopnik Schmid, Jana; https://orcid.org/ +5 more
core +1 more source
ABSTRACT Introduction The Dobbs v. Jackson Women's Health Organization United States (US) Supreme Court decision exacerbated inequitable access to abortion rights in the United States. This study aimed to determine the degree of agreement on which strategies should be prioritized to restore, protect, and expand abortion access. Methodology From July to
Sarah Pickering +54 more
wiley +1 more source
Monocyte/macrophages may exert prominent roles in macrophage activation syndrome
Secondary Hemophagocytic lymphohistiocytosis (sHLH) is a life-threatening complication mostly occurs in adult patients with rheumatic disease, infection or lymphoma. To adequately steer treatment, clear discrimination of sHLH entities is essential.
Dongfei Yin, Jingshi Wang, Zhao Wang
doaj +1 more source

