Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

Arch Neurol. 1968 Jun;18(6):603-18. doi: 10.1001/archneur.1968.00470360025002.
No abstract available

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Ataxia
  • Cerebrospinal Fluid Proteins
  • Child
  • Demyelinating Diseases
  • Electrophysiology
  • Female
  • Gait
  • Genes, Dominant
  • Genes, Recessive
  • Humans
  • Hypertrophy
  • Male
  • Middle Aged
  • Muscular Atrophy / genetics*
  • Neural Conduction
  • Pedigree
  • Peripheral Nerves / physiology
  • Peripheral Nervous System Diseases / genetics*
  • Polyneuropathies
  • Prognosis

Substances

  • Cerebrospinal Fluid Proteins