• Login
  • Search
  • Login
  • Search
E-Poster Portal
The International Child Neurology Congresses
  • ePosters
  • Presenters
  1. You are here:  
  2. Home
  3. 101.Arthrogryposis multiplex congenita and scn1a mutations: another reported case and treatment guidance
Details
Alyssa Robison
Category: ePosters
Hits: 81
  • Alyssa Robison
Previous article: 100.A case report of sequential seizure semiology as a sign of genetic etiology Prev Next article: 102.Paraneoplastic guillain-barre syndrome: a case report and call for modified diagnostic criteria Next