More recently, several journals proposed the name 'granulomatosis with polyangiitis' in a 2011 editorial.

Article: Cardiac involvement in granulomatosis with polyangiitis (Wegener granulomatosis).

Churg-Strauss syndrome (also known as eosinophilic granulomatosis with polyangiitis, EGPA, or allergic granulomatosis) is a medium and small vessel autoimmune vasculitis, leading to necrosis.

Hypomorphic RAG mutations are seen in patients with midline granulomatous disease; an autoimmune disorder that is commonly seen in patients with granulomatosis with polyangiitis (Wegenr's disease) and NK/T cell lymphomas.

It has also been shown that up to 70% of patients with granulomatosis with polyangiitis (previously known as Wegener's granulomatosis) are chronic nasal carriers of Staphylococcus aureus, with carriers having an eight times increased risk of relapse.

ANCAs are associated with small vessel vasculitides including granulomatosis with polyangiitis (previously known as Wegener's granulomatosis), microscopic polyangiitis, primary pauciimmune necrotizing cresentric glomerulonephritis (a type of renal-limited microscopic polyangiitis), Churg-Strauss syndrome and drug induced vasculitides.

It is sometimes considered to be part of a spectrum with Wegener's granulomatosis.

The exact cause of Wegener's granulomatosis is not known.

Wegener's granulomatosis: prospective clinical and therapeutic experience with 85 patients for 21 years.

In diseases such as Wegener's granulomatosis, immune suppression is required.

The press was now a condition, like lupus erythematosus or Wegener's granulomatosis.

Sera from eight patients with Wegener's granulomatosis were studied.

Wegener's granulomatosis is usually suspected only when a patient has had unexplained symptoms for a long period of time.

A systematic review of 84 trials examined the evidence for various treatments in Wegener's granulomatosis.

This includes certain forms of vasculitis (such as Wegener's granulomatosis, in which it was not effective).

Wegener's granulomatosis is one of the autoimmune conditions that may precipitate hearing loss.

Similar treatment abolished positive staining using sera from patients with Wegener's granulomatosis.

Whether this autoantibody has direct pathogenic importance, as in Wegener's granulomatosis, remains to be determined.

These granulomas are the main reason for the appellation of "Wegener's granulomatosis", although it is not an essential feature.

House at first thinks it's Wegener's granulomatosis.

Differentiation from Wegener's granulomatosis is not difficult.

Wegener's granulomatosis, an autoimmune condition, may precipitate hearing loss.

Other diseases that involve connective tissue, such as sarcoidosis and Wegener's granulomatosis.

It is most commonly due to Wegener's granulomatosis or Goodpasture's syndrome.

Wegener's granulomatosis is a rare disease.

It is also used to treat certain types of blood vessel disease (such as Wegener's granulomatosis, microscopic polyangiitis).

Emotional support and information for patients with life-threatening uncommon Wegener's granulomatosis and related vasculitis illnesses.

Lung nodules can also occur in immune disorders such as rheumatoid arthritis or Wegener's granulomatosis.

Colvin took ill with Wegener's granulomatosis, a rare inflammation of blood vessels, which nearly took his life.

Although this disease was known before Wegener's description, since the 1950s it has been called by the name Wegener's granulomatosis.

Eight patients with Wegener's granulomatosis were all positive, showing the characteristic granular, diffuse cytoplasmic immunofluorescence pattern.