Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the
most common systemic vasculitis in children, characterized by diverse clinical …

IgA, previously called Henoch-Schönlein vasculitis, is an essential immune component that
drives the host immune response to the external environment. As IgA has the unique …

The term “vasculitis” refers to a group of rare immune‐mediated diseases characterized by
the dysregulated immune system attacking blood vessels located in any organ of the body …

Immunoglobulin-A vasculitis (IgAV) is classically a childhood small-sized blood vessel
vasculitis with predominant involvement of the skin. Gastrointestinal and joint manifestations …

IgA vasculitis with nephritis (IgAVN) shares many pathogenetic features with IgA
nephropathy (IgAN). The purpose of this review is to describe our current understanding of …

What are the challenges ahead and how have we responded so far when it comes to the
non-granulomatous systemic vasculitis, characterized mainly by deposits of IgA immune …

Objective Adult‐onset IgA vasculitis (Henoch‐Schönlein)(Ig AV) is a rare systemic vasculitis
characterized by IgA1‐dominant deposits. The treatment of adult‐onset Ig AV is …

Abstract Purpose of Review The purpose of the study is to perform an update on the current
knowledge on genetics, clinical manifestations, and therapy in immunoglobulin A vasculitis …

Muscle bulk in adult healthy humans is highly variable even after height, age, and sex are
accounted for. Low muscle mass, due to fewer and/or smaller constituent muscle fibers …

Objective: Immunoglobulin A vasculitis/Henoch–Schönlein purpura (IgAV/HSP) is a systemic
vasculitis involving small vessels with the deposition of immune complexes containing IgA. It …