Results 31 to 40 of about 22,345 (254)

Diagnostic guidelines for HLH (HLH-2004 criteria) [15].

open access: yes, 2021
Diagnostic guidelines for HLH (HLH-2004 criteria) [15].
Lei Wang (6656)   +7 more
core   +1 more source

Simple Evaluation of Clinical Situation and Subtypes of Pediatric Hemophagocytic Lymphohistiocytosis by Cytokine Patterns

open access: yesFrontiers in Immunology, 2022
BackgroundHemophagocytic lymphohistiocytosis (HLH) is a rapidly fatal disease caused by immune dysregulation. Early initiation of treatment is imperative for saving lives.
Xiao-Jun Xu   +15 more
doaj   +1 more source

Epidemiological investigation of hemophagocytic lymphohistiocytosis in China

open access: yesOrphanet Journal of Rare Diseases, 2021
Background Currently, most research on hemophagocytic lymphohistiocytosis (HLH) have focused on etiology and therapy, leaving few epidemiological reports. The published studies of China are mainly regional investigations.
Shuyan Yao   +16 more
doaj   +1 more source

Incidence and survival of haemophagocytic lymphohistiocytosis: A population‐based cohort study from England

open access: yes, 2022
Background: Haemophagocytic lymphohistiocytosis (HLH) is a rare hyper-inflammatory condition with poor outcomes. Objectives: Few population-based estimates of the incidence and survival in adults exist. We aimed to provide these data for England. Methods:
Lucy Elliss‐Brookes   +23 more
core   +1 more source

Niemann - Pick disease associated with hemophagocytic syndrome

open access: yesTurkish Journal of Hematology, 2010
Hemophagocytic lymphohistiocytosis (HLH) is a disease characterized by phagocytosis of blood cells by macrophages within the lymphoreticular tissue. It can develop secondary to some diseases or be familial as a result of genetic mutations.
Serap Karaman   +3 more
doaj   +1 more source

Hemophagocytic Lymphohistiocytosis after ChAdOx1 nCoV-19 Coronavirus Vaccination in a Patient with no Known Comorbidities

open access: yesIndian Journal of Medical Specialities, 2022
Hemophagocytic lymphohistiocytosis (HLH) is an inflammatory condition where there is marked cytopenia and large-scale activation of macrophages and CD8+ cytotoxic T cells.
Nitin Rai   +4 more
doaj   +1 more source

HLH-30/TFEB is abnormally activated in alfa-1(ok3062).

open access: yes, 2020
(A) Representative images of HLH-30::GFP expression patterns in wild-type or alfa-1(ok3062) C. elegans under well-fed (upper panels) or starvation (lower panels) conditions. Enlarged images of the boxed areas are shown in each panel.
Yon Ju Ji (3359057)   +5 more
core   +1 more source

Hemophagocytic lymphohistiocytosis secondary to dengue fever

open access: yesEuropean Journal of Case Reports in Internal Medicine
Hemophagocytic 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
doaj   +1 more source

HLH-1 Modulates Muscle Proteostasis During Caenorhabditis elegans Larval Development

open access: yesFrontiers 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
doaj   +1 more source

Data_Sheet_1_High Mortality of HLH in ICU Regardless Etiology or Treatment.docx

open access: yes, 2021
Background: Adult hemophagocytic lymphohistiocytosis (HLH) is highly lethal in the ICU. The diagnostic and therapeutic emergency that HLH represents is compounded by its unknown pathophysiological mechanisms.
Marc Gainnier (64989)   +10 more
core   +1 more source

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