Mutations of familial hemophagocytic lymphohistiocytosis (FHL) related genes and abnormalities of cytotoxicity function tests in patients with macrophage activation syndrome (MAS) occurring in systemic juvenile idiopathic arthritis (sJIA)

Lignende værker

• Familial Hemophagocytic Lymphohistiocytosis: When Rare Diseases Shed Light on Immune System Functioning
  af: Sieni, Elena, et al.
  Udgivet: (2014)
• Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry
  af: Cetica, Valentina, et al.
  Udgivet: (2016)
• Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis
  af: Meazza, Raffaella, et al.
  Udgivet: (2014)
• Molecular basis of familial hemophagocytic lymphohistiocytosis
  af: Cetica, Valentina, et al.
  Udgivet: (2010)
• PReS-FINAL-2186: Monoallelic mutations of familial hlh-related genes associated to macrophage activation syndrome
  af: Bracaglia, C, et al.
  Udgivet: (2013)