Results 91 to 100 of about 13,346 (189)
ABSTRACT Background and Aims Wilson's disease (WD) is a genetic disorder of copper metabolism in which early diagnosis remains challenging, particularly in acute liver failure (ALF). Relative exchangeable copper (REC) and exchangeable copper (CuEXC) are emerging biomarkers for diagnosis and monitoring, but data from larger cohorts are limited.
Sebastian Köhrer +10 more
wiley +1 more source
Hemophagocytic lymphohistiocytosis in adults
Dear Sir, I read with interest a recent article by Antonodimitrakis and colleagues in your journal presenting a case of acquired hemophagocytic lymphohistiocytosis (HLH) in a 60-year-old woman suffering from diabetes mellitus type 2 (1). The reported patient developed a life-threatening HLH associated with a reactivation of an Epstein–Barr virus ...
openaire +2 more sources
Familial hemophagocytic lymphohistiocytosis [PDF]
T E, Herman, M J, Siegel
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The article presents a clinical case of successful application of high doses of normal human immunoglobulin in a patient with secondary hemophagocytic syndrome associated with adenovirus infection, who was in the clinic of infectious diseases of the ...
A. A. Selʹkina +10 more
doaj +1 more source
Plenary Abstracts Session & Oral Presentations
HemaSphere, Volume 10, Issue S1, June 2026.
wiley +1 more source
Nonfamilial hemophagocytic lymphohistiocytosis [PDF]
Evans R, Fernández-Pérez, Abdi A, Jama
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Cyclic Fevers in Pregnancy: A Case of Parvovirus-Related Hemophagocytic Lymphohistiocytosis. [PDF]
Rich DJ +4 more
europepmc +1 more source
Hemophagocytic lymphohistiocytosis presenting with persistent hyperlactatemia: a distinct phenotype. [PDF]
Wang D, Guo L.
europepmc +1 more source

