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Macrophage activation syndrome in juvenile dermatomyositis: a case report and a comprehensive review of the literature
Macrophage activation syndrome in juvenile dermatomyositis: a case report and a comprehensive review of the literature
Macrophage activation syndrome (MAS) is a severe and life-threatening syndrome associated with autoimmune diseases. The co...
Predictors of persisting pain in children with Juvenile Idiopathic Arthritis: a case control study nested in the ReACCh-Out cohort
Predictors of persisting pain in children with Juvenile Idiopathic Arthritis: a case control study nested in the ReACCh-Out cohort
To identify baseline predictors of persisting pain in children with Juvenile Idiopathic Arthritis (JIA), relative to patie...
Structural ultrasound of joints and tendons in healthy children: development of normative data
Structural ultrasound of joints and tendons in healthy children: development of normative data
Musculoskeletal ultrasound is a well accessible technique to assess disease activity in children with juvenile idiopathic ...
Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositis
Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositis
Juvenile dermatomyositis (jDM) is the most common idiopathic inflammatory myopathy of childhood. Amyopathic or hypomyopath...
Panniculitis with late onset enthesitis-related arthritis: a case report
Panniculitis with late onset enthesitis-related arthritis: a case report
Panniculitis, a type of inflammation of subcutaneous fat, is a relatively uncommon condition that usually presents as infl...
A case of neonatal sweet syndrome associated with mevalonate kinase deficiency
A case of neonatal sweet syndrome associated with mevalonate kinase deficiency
Sweet syndrome (SS), also known as acute febrile neutrophilic dermatosis, is an immunologic syndrome characterized by wide...
Subcutaneous tocilizumab in the management of non-infectious uveitis in children: a brief report
Subcutaneous tocilizumab in the management of non-infectious uveitis in children: a brief report
Tocilizumab is a humanized monoclonal antibody that acts as an IL-6 receptor antagonist. Intravenous tocilizumab is consid...
The impact of the COVID-19 pandemic on patients with juvenile idiopathic inflammatory myopathies
The impact of the COVID-19 pandemic on patients with juvenile idiopathic inflammatory myopathies
Throughout the COVID-19 pandemic, there have been concerns regarding the risks of infection in patients with autoimmune di...
Childhood-onset rheumatoid arthritis at a tertiary hospital in Senegal, West Africa
Childhood-onset rheumatoid arthritis at a tertiary hospital in Senegal, West Africa
Childhood-onset rheumatoid arthritis (CORA), known as rheumatoid factor (RF)-positive juvenile idiopathic arthritis is a t...
Disease evolution in systemic juvenile idiopathic arthritis: an international, observational cohort study through JIRcohort
Disease evolution in systemic juvenile idiopathic arthritis: an international, observational cohort study through JIRcohort
Systemic juvenile idiopathic arthritis (systemic JIA) is a severe disease with both systemic and joint inflammation. This ...
Survey of adolescents’ needs and parents’ views on sexual health in juvenile idiopathic arthritis
Survey of adolescents’ needs and parents’ views on sexual health in juvenile idiopathic arthritis
Although the advent of new therapeutics for juvenile idiopathic arthritis (JIA) patients has considerably lessened the imp...
Extreme Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA): a discrete group of patients
Extreme Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA): a discrete group of patients
Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome is the most common periodic fever...
Successful experience of tofacitinib treatment in patients with Fibrodysplasia Ossificans Progressiva
Successful experience of tofacitinib treatment in patients with Fibrodysplasia Ossificans Progressiva
Fibrodysplasia ossificans progressive (FOP) is an ultra-rare genetic disorder that is caused by a mutation in the ACVR1 ge...
Pediatric-onset limited ANCA-associated vasculitis arising during pre-existing chronic recurrent multifocal osteomyelitis
Pediatric-onset limited ANCA-associated vasculitis arising during pre-existing chronic recurrent multifocal osteomyelitis
Granulomatosis with polyangiitis (GPA) is an autoimmune disease characterized by chronic vasculitis involving small to med...
Elevated serum IFN-γand IFN-γ/IL-6 ratio in Kikuchi-Fujimoto disease
Elevated serum IFN-γand IFN-γ/IL-6 ratio in Kikuchi-Fujimoto disease
Kikuchi-Fujimoto disease (KFD) is typically a benign, self-limiting inflammatory disease. The diagnosis of KFD can be chal...
A case series on recurrent and persisting IgA vasculitis (Henoch Schonlein purpura) in children
A case series on recurrent and persisting IgA vasculitis (Henoch Schonlein purpura) in children
IgA vasculitis (IgAV) is a small vessel vasculitis that is more common in childhood. Very limited evidence exists on patie...
A novel PRKDC mutation caused B lymphocytes V(D)J rearrangement disorder in the SLE-DAH like symptoms patient
A novel PRKDC mutation caused B lymphocytes V(D)J rearrangement disorder in the SLE-DAH like symptoms patient
Analyzed the clinical features and treatment process of the patient suffering from immunodeficiency with systemic lupus er...
Impact of SARS-CoV-2 on the clinical presentation of juvenile idiopathic inflammatory myopathies
Impact of SARS-CoV-2 on the clinical presentation of juvenile idiopathic inflammatory myopathies
Growing evidence suggests that infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may trigger idi...
Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility
Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility
Kawasaki disease (KD) is an acute pediatric vasculitis affecting genetically susceptible infants and children. Although th...
Monoarticular juvenile idiopathic arthritis as a distinct clinical entity A proof-of-concept study
Monoarticular juvenile idiopathic arthritis as a distinct clinical entity A proof-of-concept study
Currently, monoarticular Juvenile Idiopathic Arthritis (monoJIA) is included in the ILAR classification as oligoarticular ...
C1-C2 subluxation in enthesitis-related arthritis: two case reports and literature review of ten cases
C1-C2 subluxation in enthesitis-related arthritis: two case reports and literature review of ten cases
C1-C2 subluxation is a rare complication of enthesitis-related arthritis (ERA). If left untreated, it may lead to function...
Identifying circRNA-associated-ceRNA networks in juvenile spondyloarthropathies patients
Identifying circRNA-associated-ceRNA networks in juvenile spondyloarthropathies patients
Juvenile spondyloarthropathies (JSpA) are defined as a heterogeneous group of diseases that start before the age of 16. Th...