A case of familial ALS due to multi-system proteinopathy 1 and Huntington disease

Amyotroph Lateral Scler Frontotemporal Degener. 2015 Mar;16(1-2):124-6. doi: 10.3109/21678421.2014.952238. Epub 2014 Sep 10.
No abstract available

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / etiology*
  • Brain / pathology
  • Glial Fibrillary Acidic Protein / metabolism
  • Humans
  • Huntington Disease / complications*
  • Male
  • Middle Aged
  • Neurons / metabolism
  • TDP-43 Proteinopathies / complications*

Substances

  • Glial Fibrillary Acidic Protein