Back to search

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotypeDOI 10.1186/1546-0096-11-s1-a158
The expanding spectrum of clinical phenotypes associated with PSTPIP1 mutations: from PAPA to PAMI syndrome and beyond.Semantic proximity
P02-006 - A novel PSTPIP1 mutation in PAPA syndromeSemantic proximity
A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndromeSemantic proximity
P02-018 - PSTPIP1 gene mutations in periodic fever patientsSemantic proximity
Rare cases of PAMI syndrome in both father and son with the same missense mutation in PSTPIP1 gene and literature review.Semantic proximity
PW02-031 - Genetic and clinical manifestations of CAPSSemantic proximity
Update of Emerinopathies’ clinical-genetic spectrum: the French network experienceSemantic proximity
Comorbidities or different entities? Phenotype variability associated with PSENEN mutations.Semantic proximity
Genetic lessons learned from pathogenic variants in KRT1.Semantic proximity
The true culprit within the SPINK1 p.N34S-containing haplotype is still at large.Semantic proximity
Mutation of PACS1: the milder end of the spectrum.Semantic proximity
A global map of associations between types of protein posttranslational modifications and human genetic diseasesSemantic proximity
Select a neighboring publication to make it the new centre.