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A Patient Heterozygous for R92Q Mutation with Periodic Fever and Aphthous Stomatitis, Pharyngitis, and Adenitis (Pfapa) Syndrome-Like Phenotype
(Turkish J Pediatrics, 2018)
Tumor necrosis factor receptor associated periodic syndrome (TRAPS) is an autosomal dominant disease caused by mutations located on the type 1 tumor necrosis factor receptor (TNFRSF1A) gene. Here we present a 3-year-old ...
Predictors of Methotrexate Response in Turkish Children with Oligoarticular and Polyarticular Juvenile Idiopathic Arthritis
(Turkish J Pediatrics, 2017)
Methotrexate (MTX) is the most commonly used disease modifying antirheumatic drug in juvenile idiopathic arthritis (JIA). We aimed to define predictor factors for response to MTX in Turkish children with oligo- and ...
Vasculitis: Do We Know More To Classify Better?
(Springer, 2015)
The systemic vasculitides are a heterogeneous group of disorders characterized by the inflammation of blood vessels. The development and implementation of advanced diagnostic tests and genetic studies have resulted in ...