Three German fibrinogen Aα-chain amyloidosis patients with the p.Glu526Val mutation

This publication has 22 references indexed in Scilit:

• Structural analyses of fibrinogen amyloid fibrils
  Amyloid, 2007
• Molecular Basis of Fibrinogen Deficiency
  Pathophysiology of Haemostasis and Thrombosis, 2006
• Successful Hepatorenal Transplantation in Hereditary Amyloidosis Caused by a Frame-Shift Mutation in Fibrinogen Aa -Chain Gene
  American Journal of Transplantation, 2006
• Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aα chain gene
  Kidney International, 2005
• Ostertag revisited: The inherited systemic amyloidoses without neuropathy
  Amyloid, 2005
• Cleavage of AL amyloid proteins and AL amyloid deposits by cathepsins B, K, and L
  The Journal of Pathology, 2004
• Fibrinogen Act chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French family
  Amyloid, 1998
• Fibrinogen Aa Chain Leu 554: an African-American kindred with late onset renal amyloidosis
  Amyloid, 1998
• The molecular basis of renal amyloidosis in Irish-American and Polish-Canadian kindreds
  QJM: An International Journal of Medicine, 1996
• Variant apolipoprotein AI as a major constituent of a human hereditary amyloid
  Biochemical and Biophysical Research Communications, 1988