Hereditary cardiac amyloidosis associated with the transthyretin Ile122 mutation in a white man

Lignende værker

• Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile)
  af: Nágela S. V. Nunes, et al.
• Transthyretin Ile 122 and cardiac amyloidosis in African-Americans. 2 case reports.
  af: Jacobson, D R, et al.
  Udgivet: (1997)
• A case of cardiac amyloidosis in an elderly Japanese patient with amyloidogenic transthyretin Val122Ile variant
  af: Ono, Ryohei, et al.
  Udgivet: (2020)
• Sex Differences in the Phenotype of Transthyretin Cardiac Amyloidosis due to Val122Ile Mutation: Insights from Non-Invasive Pressure-Volume Analysis
  af: Batra, Jaya, et al.
  Udgivet: (2020)
• Hereditary transthyretin amyloidosis
  af: T. A. Adyan, et al.
  Udgivet: (2020-01-01)