TNFRSF1A gen and R92Q and P46L variants. Association with other inflammatory diseases

Gelijkaardige items

• Capillaroscopic findings in children and adolescents with raynaud’s phenomenon: results from study in 92 patients
  door: Montesinos, Berta Lopez, et al.
  Gepubliceerd in: (2014)
• Infectious adverse effects during treatment with IL-1 inhibitors in patients with systemic juvenile idiopathic arthritis and autoinflammatory diseases
  door: Fernandez-Silveira, Laura, et al.
  Gepubliceerd in: (2014)
• NLRP3 Q703K and TNFRSF1A R92Q mutations in a patient with auto inflammatory disease
  door: von Mühlenen, I, et al.
  Gepubliceerd in: (2015)
• PReS-FINAL-2235: Overlap of homozygous TNFRSF1A R92Q mutation with MEVF E148Q mutation versus homozygous TNFRSF1A R92Q mutation: difference in clinical profile in two sisters from Oman
  door: Abdwani, R, et al.
  Gepubliceerd in: (2013)
• The intracellular signalling pathway signature (the signalome) in PBMCs in the presence of a common TRAPS-associated genetic variant, TNFRSF1A p.(Arg121Gln) (legacy p.R92Q) is distinct from normal PBMCs and from other pathogenic variants
  door: Bybee, A, et al.
  Gepubliceerd in: (2015)