Background. Behçet’s disease is a rare type of vasculitis. Validated activity and damage scores were developed for vasculitis patients in order to allow a better way to evaluate disease activity and decide treatment plans. Objective. The main objective was to compare two vasculitis activity scores applied to a group of patients diagnosed with Behçet’s disease and establish correlations between them, damage and the need for immunosuppressive therapy. The secondary objective was to evaluate the connection between damage progression, classical immunosuppressant therapy and long-term cortisone use. Methods. A study was performed on a cohort of patients diagnosed with Behçet’s disease according The International Criteria for Behçet‘s Disease...
OBJECTIVES: Patient-reported outcomes are increasingly accepted to be major domains in chronic disor...
Aim: Currently, several different instruments are used to measure disease activity and extent in cli...
Behçet’s disease is a multi-organ inflammatory disorder with systemic vasculitis of unknown etiology...
Objective. Assessment of disease activity in vasculitis can be achieved using the BVAS, a clinical c...
The continuing morbidity of patients with vasculitis, despite the improved prognosis with aggressive...
Methods. A total of 238 patients with vasculitis from seven countries in Europe were evaluated at a ...
The systemic vasculitides are a group of rare, chronic, relapsing, but often progressive inflammator...
Objective: To develop and validate the evidence-based and consensus-based Behçet's Syndrome Overall ...
OBJECTIVE: To develop and validate the evidence-based and consensus-based Behçet's Syndrome Overall ...
Background: Objective scoring systems of disease activity and disease-associated damage have proven ...
Antineutrophil cytoplasm antibody associated vasculitis has been transformed from life-threatening c...
Objective: Patient-reported outcomes are increasingly accepted to be major domains in chronic disord...
Objectives: To compare patients' and physician's global assessment of disease activity in ANCA-assoc...
OBJECTIVES: The disease activity of Behçet's disease is inadequately defined, and there is no consen...
Systemic vasculitides are a group of heterogeneous conditions with overlapping patterns of clinical ...
OBJECTIVES: Patient-reported outcomes are increasingly accepted to be major domains in chronic disor...
Aim: Currently, several different instruments are used to measure disease activity and extent in cli...
Behçet’s disease is a multi-organ inflammatory disorder with systemic vasculitis of unknown etiology...
Objective. Assessment of disease activity in vasculitis can be achieved using the BVAS, a clinical c...
The continuing morbidity of patients with vasculitis, despite the improved prognosis with aggressive...
Methods. A total of 238 patients with vasculitis from seven countries in Europe were evaluated at a ...
The systemic vasculitides are a group of rare, chronic, relapsing, but often progressive inflammator...
Objective: To develop and validate the evidence-based and consensus-based Behçet's Syndrome Overall ...
OBJECTIVE: To develop and validate the evidence-based and consensus-based Behçet's Syndrome Overall ...
Background: Objective scoring systems of disease activity and disease-associated damage have proven ...
Antineutrophil cytoplasm antibody associated vasculitis has been transformed from life-threatening c...
Objective: Patient-reported outcomes are increasingly accepted to be major domains in chronic disord...
Objectives: To compare patients' and physician's global assessment of disease activity in ANCA-assoc...
OBJECTIVES: The disease activity of Behçet's disease is inadequately defined, and there is no consen...
Systemic vasculitides are a group of heterogeneous conditions with overlapping patterns of clinical ...
OBJECTIVES: Patient-reported outcomes are increasingly accepted to be major domains in chronic disor...
Aim: Currently, several different instruments are used to measure disease activity and extent in cli...
Behçet’s disease is a multi-organ inflammatory disorder with systemic vasculitis of unknown etiology...