Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian children

Documenti analoghi

• The Easy Handgrip Test as a Tool for Assessing Motor Fatigability in Children With Charcot‐Marie‐Tooth Disease Type 1A
  di: Ester da Silva Estevam, et al.
  Pubblicazione: (2025)
• Monoclonal gammopathy‐associated peripheral neuropathies: Uncovering pearls and challenges
  di: Trajano Aguiar Pires Gonçalves, et al.
  Pubblicazione: (2024)
• Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology
  di: Antonino Uncini, et al.
  Pubblicazione: (2024)
• Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies
  di: Alessandro Geroldi, et al.
  Pubblicazione: (2024)
• Cytokines and chemokines in patients with chronic inflammatory demyelinating polyradiculoneuropathy and multifocal motor neuropathy: A systematic review
  di: Claudia Cutellè, et al.
  Pubblicazione: (2024)