Duchenne muscular dystrophy (DMD) is a lethal X-linked recessive muscle disease due to
defect on the gene encoding dystrophin. The lack of a functional dystrophin in muscles results …

… 1 with T1D, analyzed using electron microscopy, and showing a granulocyte (GN) and a
lymphocyte (L) in a microvessel of the exocrine tissue (left panel), and a GN adjacent to acinar …

Background The laboratory diagnosis of hereditary spherocytosis commonly relies on NaCl-based
or glycerol-based red cell osmotic fragility tests; more recently, an assay directly …

Background. Antibodies directed against alloantigens are implicated in the pathogenesis of
several immune reactions complicating transplantation, including humoral rejection after …

… The asymptomatic increase of serum bile acid levels >160 μmol/L that we observed at week
20 and 24 was likely due to the fact that BLV was self-administered before blood sampling, …

… ; total bilirubin, 0.12 to 1.1 mg/dL; serum ferritin, 15 to 150 µg/L; D-dimer <500 µg/L; and C-reactive
protein <0.5 mg/dL. Numbers in bold type indicate statistical significance. …

… L indicates the process of a transplanted hGFAP-positive cell extending toward the cell body
(boxed area in J). LV, lateral ventricle; Cx, cortex; Str, striatum. Scale bar in E = 50 μm for C–…

Small extracellular vesicles (EVs) are able to pass from the central nervous system (CNS)
into peripheral blood and contain molecule markers of their parental origin. The aim of our …

Background Severe acute respiratory syndrome coronavirus 2 is a recently discovered
pathogen responsible of coronavirus disease 2019 (COVID-19). The immunological changes …

Objective MicroRNAs (miRNAs) are regulatory molecules, which have been addressed as
potential biomarkers and therapeutic targets in rheumatic diseases. Here, we investigated the …