Contemporary genetic research has provided evidences that angioedema represents a
diverse family of disorders related to kinin metabolism, with a much greater genetic complexity …

Nasu-hakola disease (NHD) is a rare disease characterized by bone cysts and fractures,
frontal lobe syndrome, and progressive presenile dementia. NHD may be the prototype of …

Hereditary angioedema (HAE) is becoming much more genetically complex than was initially
considered. Thus, the role of HAE genetics is expanding beyond research laboratories, …

Objective Transcription factor forkhead box protein 3 (Foxp3) specifically characterizes the
thymically derived naturally occurring regulatory T cells (Tregs). Limited evidence indicates …

Background The consensus documents published to date on hereditary angioedema with C1
inhibitor deficiency (C1‐ INH ‐ HAE ) have focused on adult patients. Many of the previous …

The induction of the autophagy machinery, a process for the catabolism of cytosolic proteins
and organelles, constitutes a crucial mechanism in innate immunity. However, the …

Bone morphogenetic proteins (BMPs) are pleiotropic secreted proteins, structurally related to
transforming growth factor (TGF)-β and activins. BMPs play pivotal roles in the regulation of …

A serosurvey of IgG antibodies against severe acute respiratory coronavirus 2 (SARS-CoV-2)
was performed during March and April 2020. Among 6,586 leftover sera, 24 (0.36%) were …

(Fig 1, B). Nevertheless, CMV-specific T-cell responses were detectable by 4.5 months post-BMT
with a stimulation index of 61 and robust IFN-g, TNF-a secretion (536.5 pg/mL and 11.4 …

A Knowledge, Attitudes and Practices (KAP) study was conducted at the end of May 2021
engaging 1456 healthcare workers (HCWs) from 20 hospitals throughout Greece. Acceptance …