Citation Tools
PDFNeurological rarities
IgG4-related disease: a rare but treatable cause of refractory intracranial hypertension
Download to a citation manager
Download the citation for this article by clicking on one of the following citation managers:
- Cite this article as:
- IgG4-related disease: a rare but treatable cause of refractory intracranial hypertension
Other content recommended for you
- IgG4-related hypertrophic pachymeningitis with chronic subdural haematoma
- A nationwide survey of hypertrophic pachymeningitis in Japan
- Rituximab for corticosteroid-resistant relapsing IgG4-related intracranial pachymeningitis: report of two cases
- Advances in the diagnosis and management of IgG4 related disease
- IgG4-related disease presenting with multiorgan involvement
- Pathological findings of hypertrophic pachymeningitis associated with eosinophilic granulomatosis with polyangiitis
- Clinicopathological case: headache and systemic inflammatory illness—Occam vs Hickam
- The enigmatic immunoglobulin G4-related disease and its varied cardiovascular manifestations
- Plasmablasts as a biomarker for IgG4-related disease, independent of serum IgG4 concentrations
- Hypertrophic pachymeningoencephalitis associated with temporal giant cell arteritis