Early intervention with tafamidis provides long-term benefit in delaying neurological progression in patients with transthyretin familial amyloid polyneuropathy

Gelijkaardige items

• Early intervention with tafamidis provides long-term (5.5-year) delay of neurologic progression in transthyretin hereditary amyloid polyneuropathy
  door: Waddington Cruz, Márcia, et al.
  Gepubliceerd in: (2016)
• Influence of baseline neurologic severity on disease progression and the associated disease-modifying effects of tafamidis in patients with transthyretin amyloid polyneuropathy
  door: Leslie Amass, et al.
  Gepubliceerd in: (2018-12-01)
• Influence of baseline neurologic severity on disease progression and the associated disease-modifying effects of tafamidis in patients with transthyretin amyloid polyneuropathy
  door: Amass, Leslie, et al.
  Gepubliceerd in: (2018)
• Tafamidis reduces disease progression in patients with transthyretin familial amyloid polyneuropathy: supportive post-hoc analyses of a pivotal trial
  door: Keohane, Denis, et al.
  Gepubliceerd in: (2015)
• Tafamidis delays neurological progression comparably across Val30Met and non‐Val30Met genotypes in transthyretin familial amyloid polyneuropathy
  door: Gundapaneni, B. K., et al.
  Gepubliceerd in: (2017)