Results 181 to 190 of about 202,744 (245)
Objective Antiphospholipid syndrome (APS) is a thromboinflammatory disorder characterized by clinical and mechanistic heterogeneity that complicates early diagnosis and hinders targeted treatment. We aimed to identify distinct molecular endotypes among antiphospholipid antibody (aPL)–positive patients using whole‐blood transcriptomics.
Amala Ambati +13 more
wiley +1 more source
Epstein-Barr Virus Silences GSDME and Pyroptosis in Gastric Cancer. [PDF]
Lee MH, Lee JY, Kim JY, An YR, Lee SK.
europepmc +1 more source
ABSTRACT Background With the development of new sequencing technologies, metagenomic next‐generation sequencing (mNGS) has become a diagnostic tool for respiratory tract infections. Patients with cancer may develop pneumonia caused by infections or antitumor therapy.
Rong Qin +4 more
wiley +1 more source
Breast Implant-Associated Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma. [PDF]
Maerten T +4 more
europepmc +1 more source
Acute Pancreatitis as an Extrahepatic Complication of Acute Hepatitis E Infection: A Case Report
ABSTRACT Clinicians should consider Hepatitis E Virus (HEV) a rare but significant etiology alongside established primary triggers, including gallstones and alcohol. Early HEV screening for hepatic and pancreatic dysfunction is required to improve care and avoid unnecessary interventions, especially in endemic regions.
Syed Abdur Rehman Shah +4 more
wiley +1 more source
Portal Vein Thrombosis Due to Concomitant Cytomegalovirus and Epstein-Barr Virus Infection: An Underestimated Complication. [PDF]
AlQahtani SY.
europepmc +1 more source
ABSTRACT Phagocytic activity of mesothelial cells is a rare phenomenon requiring careful differentiation from histiocytic hemophagocytosis to ensure appropriate patient management, as these phenomena could exhibit distinct clinical implications. In this study, we report a case of phagocytic mesothelial cells found in pericardial effusion that developed
Hidetoshi Satomi +5 more
wiley +1 more source
Splenic Infarcts in an Adult Male with Epstein-Barr Virus Infection: A Rare Complication. [PDF]
Kalfoutzou A +4 more
europepmc +1 more source
ABSTRACT Background and Aims Crigler‐Najjar Syndrome (CNS) is a rare autosomal recessive disorder caused by uridine diphosphate glucuronosyltransferase (UGT1A1) deficiency, leading to unconjugated hyperbilirubinemia. Without treatment, patients are at high risk of kernicterus and irreversible neurological damage.
Sajad Teimoury +6 more
wiley +1 more source
Solitary thoracic Epstein-Barr virus-associated smooth muscle tumor presenting after kidney transplant: illustrative case. [PDF]
Zsigray BM +4 more
europepmc +1 more source

