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MEFV and NLRP3 gene variants in children with pfapa syndrome in sloveniaDOI 10.1186/1546-0096-12-s1-p81
Clinical features and genetic background of the periodic Fever syndrome with aphthous stomatitis, pharyngitis, and adenitis: a single center longitudinal study of 81 patients.Semantic proximity
P03-005 - MEFV heterozygous mutations in PFAPA patientsSemantic proximity
An unusual phenotype in Muckle-Wells syndrome associated with NLRP3 E311K.Semantic proximity
PW01-019 – MEFV gene mutations in 53 periodic fever patientsSemantic proximity
Significance of I313V mutation of NLPR3 gene in two pediatric patientsSemantic proximity
Clinical and subclinical features and MEFV mutation distribution in of FMF patients’ siblingsSemantic proximity
PW03-009 – Genetics of PFAPA syndromeSemantic proximity
Current understanding of the phenotypic spectrum of patients with NLRP1 variants.Semantic proximity
Post COVID recurrent fever in children with polymorphisms in the innate immunity regulator, pyrin; MEFV gene.Semantic proximity
PW02-026 - Low frequency variants of NLRP3 in CAPS patientsSemantic proximity
The clinical phenotype of Israeli patients with Q703K mutation in the NLRP3 geneSemantic proximity
Analysis of the genetic basis of periodic fever with aphthous stomatitis, pharyngitis and cervical adenitis (PFAPA) syndromeSemantic proximity
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