Associated Papers
Impact of Mediterranean Fever Gene Mutations on Clinical Characteristics in Patients With Inflammatory Bowel Disease.
Nakamura T et al.
Gastro Hep Advances, 2026
Adenine phosphoribosyltransferase (APRT) deficiency: an increasingly recognized disease.
Leow EH et al.
International Urology and Nephrology, 2025
Associations of MEFV gene variants, IL-33, and sST2 with the risk of Henoch-Schönlein purpura in children.
Ruan Y et al.
Heliyon, 2024
Possible Association of Mutations in the MEFV Gene with the Intestinal Phenotype of Behçet's Disease and Refractoriness to Treatment.
Furuta Y et al.
Journal of Clinical Medicine, 2023
Single-Center Overview of Pediatric Monogenic Autoinflammatory Diseases in the Past Decade: A Summary and Beyond.
Wang W et al.
Frontiers in Immunology, 2020
Longitudinal analysis of serum interleukin-18 in patients with familial Mediterranean fever carrying MEFV mutations in exon 10.
Wada T et al.
Cytokine, 2018
Genetics of immunoglobulin-A vasculitis (Henoch-Schönlein purpura): An updated review.
López-Mejías R et al.
Autoimmunity Reviews, 2018
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