Results 31 to 40 of about 24,724 (214)
Niemann - Pick disease associated with hemophagocytic syndrome
Turkish 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
Severe <i>Plasmodium vivax</i> Malaria Complicated by Secondary Hemophagocytic Lymphohistiocytosis, Disseminated Intravascular Coagulation, and Acute Pancreatitis: A Case Report. [PDF]
Clin Case RepABSTRACT Plasmodium vivax (P. vivax) malaria, once regarded as a comparatively benign infection, is increasingly recognized as a cause of severe, potentially life‐threatening multisystem disease. Concurrent secondary hemophagocytic lymphohistiocytosis (HLH), disseminated intravascular coagulation (DIC), and acute pancreatitis complicating P.
Nafian T +5 more
europepmc +2 more sources
High Mortality of HLH in ICU Regardless Etiology or Treatment
Frontiers in Medicine, 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.
Amandine Bichon +18 more
doaj +1 more source
Evaluation of children with haemophagocytic lymphohistiocytosis (HLH) at Red Cross War Memorial Children's Hospital 1991-2010 [PDF]
, 2011 Includes bibliographical references.Haemophagocytic Lymphohistiocytosis (HLH) is a rare haematological disorder in children. However, this is probably an underestimation due to the difficulty in diagnosing the disease.
Switala, Juli
core +1 more source
Frontiers 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
Orphanet 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
Indian 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
Journal of Pediatric Critical Care, 2016 Hemophagocytic lymphohistiocytosis (HLH) is a rare but life-threatening disease caused by uninhibited hyperinflammatory reaction that can lead to fulminant, life threatening multi organ failure and whose pathophysiology and clinical characteristics are ...
Rohit Kapoor +2 more
doaj +1 more source
HLH-30/TFEB is abnormally activated in alfa-1(ok3062).
, 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
Pakistan Armed Forces Medical Journal, 2016 Objective: To compare the mean consumption of equipotent doses of tramadol and nalbuphine for first 12 hours of post-operative analgesia, in patients undergoing gynaecological laparotomies. Study Design: Randomized clinical trial. Place and Durration of
Tanveer Hussain +3 more
doaj +2 more sources