Objective Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder characterised by fibrosis and microvascular obliteration of the skin and internal organs. Organ involvement mostly manifests after a variable period of the onset of Raynaud's phenomenon (RP). We aimed to map the incidence and predictors of pulmonary, cardiac, gastrointestinal (GI) and renal involvement in the early course of SSc. Methods In the EUSTAR cohort, patients with early SSc were identified as those who had a visit within the first year after RP onset. Incident SSc organ manifestations and their risk factors were assessed using Kaplan-Meier methods and Cox regression analysis. Results Of the 695 SSc patients who had a baseline visit within ...
Puffy fingers and Raynaud's phenomenon (RP) are important clinical predictors of the development of ...
<p><b>Objective</b>: The aim of this study was to analyse differences in clinical presentation in pa...
Objective. The clinical course of SSc depends on subtype, organ involvement and age. Few data are re...
Objective Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder charac...
OBJECTIVE Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder chara...
Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder characterised by...
Objectives To longitudinally map the onset and identify risk factors for skin sclerosis and digital ...
OBJECTIVES To longitudinally map the onset and identify risk factors for skin sclerosis and digital...
<p>Kaplan-Meier curves with 95% CI of the manifestation of any first non-RP feature after RP onset i...
Background: Systemic sclerosis (SSc) is a multisystem autoimmune disease, which is classified into a...
Systemic sclerosis (SSc) is a rare, clinically heterogeneous, severe multisystem disorder characteri...
Systemic sclerosis (SSc) is a systemic autoimmune disease charac- terised by generalized microangiop...
Systemic sclerosis (SSc) is a multisystem autoimmune disease which is classified into a diffuse cuta...
Systemic sclerosis (SSc) is a chronic connective tissue disease characterized by widespread microvas...
Puffy fingers and Raynaud's phenomenon (RP) are important clinical predictors of the development of ...
<p><b>Objective</b>: The aim of this study was to analyse differences in clinical presentation in pa...
Objective. The clinical course of SSc depends on subtype, organ involvement and age. Few data are re...
Objective Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder charac...
OBJECTIVE Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder chara...
Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder characterised by...
Objectives To longitudinally map the onset and identify risk factors for skin sclerosis and digital ...
OBJECTIVES To longitudinally map the onset and identify risk factors for skin sclerosis and digital...
<p>Kaplan-Meier curves with 95% CI of the manifestation of any first non-RP feature after RP onset i...
Background: Systemic sclerosis (SSc) is a multisystem autoimmune disease, which is classified into a...
Systemic sclerosis (SSc) is a rare, clinically heterogeneous, severe multisystem disorder characteri...
Systemic sclerosis (SSc) is a systemic autoimmune disease charac- terised by generalized microangiop...
Systemic sclerosis (SSc) is a multisystem autoimmune disease which is classified into a diffuse cuta...
Systemic sclerosis (SSc) is a chronic connective tissue disease characterized by widespread microvas...
Puffy fingers and Raynaud's phenomenon (RP) are important clinical predictors of the development of ...
<p><b>Objective</b>: The aim of this study was to analyse differences in clinical presentation in pa...
Objective. The clinical course of SSc depends on subtype, organ involvement and age. Few data are re...