Results 21 to 30 of about 732 (166)
AB0982 SERUM ALBUMIN LEVELS AND DEPRESSION IN JSLE [PDF]
Annals of the Rheumatic Diseases, 2020 Background: Albumin is a negative acute phase response protein synthesized in the liver, being an important marker of inflammation. Under inflammatory conditions, the transcapillary escape rate of albumin may increase, leading to hypoalbuminaemia. Systemic lupus erythematosus (SLE) is a chronic condition involving multiple organ systems, inducing ...
S. Ganhão +5 more
openaire +1 more source
COVID19-Related Onset and Relapses of Juvenile Systemic Lupus Erythematosus-Like Disease. [PDF]
J Paediatr Child HealthJournal of Paediatrics and Child Health, Volume 61, Issue 8, Page 1318-1321, August 2025.
Cannata C +3 more
europepmc +2 more sources
Juvenile Systemic Lupus Erythematosus Presenting with Esophagitis and Severe Oral Mucositis
Case Reports in Rheumatology, Volume 2021, Issue 1, 2021., 2021 We present a case of a previously healthy adolescent female who developed severe oral mucositis and acute esophagitis as her presenting symptoms of juvenile systemic lupus erythematosus. Mucositis involving the lips is infrequently reported in systemic lupus erythematosus, and to our knowledge, this is the first reported case of acute, non‐infectious ...
Emily Schildt +3 more
wiley +1 more source
Vasculitis in Juvenile-Onset Systemic Lupus Erythematosus
Frontiers in Pediatrics, 2019 Juvenile-onset systemic lupus erythematosus (JSLE) is a rare, heterogeneous multisystem autoimmune disease that can affect any organ, and present with diverse clinical and serological manifestations. Vasculitis can be a feature of JSLE.
Eve M. D. Smith +4 more
doaj +1 more source
AB0983 LIPID METABOLISM AND DISEASE ACTIVITY IN JSLE PATIENTS [PDF]
Annals of the Rheumatic Diseases, 2020 Background: Systemic lupus erythematosus (SLE) is an autoimmune systemic disease associated with premature atherosclerosis. Risk factors include dyslipoproteinemia, inflammation, oxidized low-density lipoprotein (LDL), hyperhomocysteinemia and antiphospholipid antibodies.
S. Ganhão +4 more
openaire +1 more source
Pediatric Rheumatology Online Journal, 2023 Background This study aimed to describe the prevalence of the various clinical features and severity of juvenile systemic lupus erythematosus (jSLE) and to assess predictors of AQP4-Ab positivity in jSLE. In addition, we assessed the relationship of AQP4-
Yasmeen Shaaban +4 more
doaj +1 more source
Ovarian dysfunction in adolescent girls with autoimmune rheumatic diseases
Pediatric Rheumatology Online Journal, 2023 Objective To explore the different menstrual and pubertal abnormalities in adolescent females with systemic autoimmune rheumatic diseases (ARD). Methods The study included adolescent girls aged 13–18 years with juvenile idiopathic arthritis (JIA ...
Mohamed Taman +3 more
doaj +1 more source
BMC Pediatrics, 2019 Background We have recognized 15 children with jSLE and the antecedent of IgA vasculitis (HSP). This association is not broadly present in the literature.
Chiharu Murata +7 more
doaj +1 more source
P24 Correlation between serum autoantibodies and clinical manifestations in jSLE [PDF]
Poster presentations, 2020 Background Systemic Lupus Erythematosus (SLE) has a large clinical spectrum, ranging from mild to severe disease. Some studies have proven correlations between specific autoantibodies and particular clinical manifestations. The aim is to assess if there is any correlation between autoantibodies and clinical manifestations in our sample.
Sara Ganhão +3 more
openaire +1 more source
Atopy in children with juvenile systemic lupus erythematosus is associated with severe disease. [PDF]
PLoS ONE, 2017 The influence of co-existing atopy on the prognosis of juvenile systemic lupus erythematosus (JSLE) was assessed in this study. Patients diagnosed with JSLE between October 2005 and April 2016 were enrolled in a prospective study and followed up for 2 ...
Ruru Guo +4 more
doaj +1 more source