Sort by: Order: Results:

Now showing items 1-4 of 4

  • Genetic Epidemiology and Cognitive Endophenotyping in Amyotrophic Lateral Sclerosis 

    Ryan, Marie (Trinity College Dublin. School of Medicine. Discipline of Clinical Medicine, 2021)
    Amyotrophic Lateral Sclerosis (ALS) is a progressive debilitating and ultimately fatal neurodegenerative disorder affecting both upper (UMN) and lower (LMN) motor neurons. While it has been long known to exist on a spectrum ...
  • Human Neurodegeneration: A Spectral EEG and TMS based Approach in Amyotrophic Lateral Sclerosis 

    McMackin, Roisin (Trinity College Dublin. School of Medicine. Discipline of Clinical Medicine, 2021)
    Amyotrophic lateral sclerosis (ALS) is defined by the neurodegeneration of upper and lower motor neurons of the corticospinal tract, resulting in progressive, terminal and incurable decline in movement, speech and swallowing ...
  • Motor and extra-motor involvement in amyotrophic lateral sclerosis 

    CHIPIKA, RANGARIROYASHE HANNAH (Trinity College Dublin. School of Medicine. Discipline of Clinical Medicine, 2019)
    Amyotrophic Lateral Sclerosis (ALS) is primarily associated with pathology in the motor cortex and corticospinal tract. Based on clinical observations, it is increasingly recognised that extra-motor symptoms add to the ...
  • Neuropsychological and Neuropsychiatric Endophenotypes in Amyotrophic Lateral Sclerosis 

    Costello, Emmet (Trinity College Dublin. School of Medicine. Discipline of Clinical Medicine, 2022)
    Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease, characterized by progressive muscle weakness and death, usually within 3-5 years from symptom onset. ALS is now recognized to be a multi-system ...