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P02-018 - PSTPIP1 gene mutations in periodic fever patientsDOI 10.1186/1546-0096-11-s1-a125
PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotypeSemantic proximity
P02-006 - A novel PSTPIP1 mutation in PAPA syndromeSemantic proximity
PW01-019 – MEFV gene mutations in 53 periodic fever patientsSemantic proximity
A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndromeSemantic proximity
The expanding spectrum of clinical phenotypes associated with PSTPIP1 mutations: from PAPA to PAMI syndrome and beyond.Semantic proximity
A Comprehensive Overview of the Hereditary Periodic Fever SyndromesSemantic proximity
[Periodic fevers: from genetics to clinical medicine].Semantic proximity
Rare cases of PAMI syndrome in both father and son with the same missense mutation in PSTPIP1 gene and literature review.Semantic proximity
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
Pyogenic arthritis, pyoderma gangrenosum, acne, and hidradenitis suppurativa (PAPASH): a new autoinflammatory syndrome associated with a novel mutation of the PSTPIP1 gene.Semantic proximity
Phenotypic Associations of PSTPIP1 Sequence Variants in PSTPIP1-Associated Autoinflammatory Diseases.Semantic proximity
A new low-penetrance TNFRSF1A mutation causing atypical periodic fever.Semantic proximity
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