MEVALONATE KINASE DEFICIENCY ASSOCIATED WITH RECURRENT LIVER DYSFUNCTION, MACROPHAGE ACTIVATION SYNDROME AND PERFORIN GENE POLYMORPHISM

Схожие документы

• Mevalonate kinase deficiency: current perspectives
  по: Favier, Leslie A, et al.
  Опубликовано: (2016)
• MACROPHAGE ACTIVATION SYNDROME AND CYTOKINE DIRECTED THERAPIES
  по: Schulert, Grant S., et al.
  Опубликовано: (2014)
• Pathogenesis of Macrophage Activation Syndrome and Potential for Cytokine-Directed Therapies
  по: Schulert, Grant S., et al.
  Опубликовано: (2014)
• Mevalonate kinase deficiency presenting as recurrent rectal abscesses and perianal fistulae
  по: Dunn, Kara, et al.
  Опубликовано: (2017)
• Novel UNC13D intronic variant disrupting a NFκB enhancer in a patient with recurrent macrophage activation syndrome and systemic juvenile idiopathic arthritis
  по: Schulert, Grant S., et al.
  Опубликовано: (2018)