e-cases: June 2003 

Others

• Combination of congenital coagulation disorders: Factor II gene mutation G20210A, Factor V Leiden gene mutation G1691A and Protein S deficiency. A family study.
  González Cocaño MC, Díaz-Golpe V, Martín S, Sánchez del Real J, Redondo MC
  Haematologica 2003; 88:(06) ECR20
  
• Acute renal cortex necrosis caused by arterial thrombosis during treatment for acute promyelocytic leukemia
  M-D Levin, M.G.H. Betjes, Th.H. v.d. Kwast, B.L wenberg, F.W.G. Leebeek
  Haematologica 2003; 88:(06) ECR21
  
• Fulminant hepatitis subsequent to reactivation of precore mutant hepatitis b virus in a patient with lymphoma treated with chemotherapy and rituximab
  José-Ángel Hernández, Raúl Diloy, David Salat, Neus del Río, Xavier Martínez, Josep-María Castellví
  Haematologica 2003; 88:(06) ECR22