Factor V Leiden mutation does not correlate with retinal vascular occlusion in white patients with Behçet’s disease

Παρόμοια τεκμήρια

• Thrombophilia: genetic polymorphisms and their association with retinal vascular occlusive disease
  ανά: CHAK, M, κ.ά.
  Έκδοση: (2001)
• Behcet's disease with retinal vascular lesions.
  ανά: Smith, R. B., κ.ά.
  Έκδοση: (1967)
• Influence of factor V Leiden on the development of neovascularisation secondary to central retinal vein occlusion
  ανά: Hvarfner, C, κ.ά.
  Έκδοση: (2003)
• Combined Central Retinal Artery and Vein Occlusion Associated with Factor V Leiden Mutation and Treated with Hyperbaric Oxygen
  ανά: Lemos, José Alberto, κ.ά.
  Έκδοση: (2015)
• The association of the PTPN22 620W polymorphism with Behçet's disease
  ανά: Baranathan, Vijay, κ.ά.
  Έκδοση: (2007)