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Poster Communications Themes

Theme 08 - Clinical Imaging and Electrophysiology

References

References

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  • Brettschneider J, Del Tredici K, Toledo JB, et al. Stages of pTDP-43 pathology in amyotrophic lateral sclerosis. Ann Neurol. 2013;74:20–38.
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  • Devlin AC, Burr K, Borooah S. et al. Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability. Nature Commun. 2015;6(1).

References

References

  • Vaughan SK, Kemp Z, Hatzipetros T. et al. Degeneration of proprioceptive sensory nerve endings in mice harboring amyotrophic lateral sclerosis-causing mutations. J Comp Neurol. 2015;523(17):2477–94.
  • Iglesias C, Sangari S, El Mendili M. et al. Electrophysiological and spinal imaging evidences for sensory dysfunction in amyotrophic lateral sclerosis. BMJ Open. 2015;5(2):e007659.
  • Sangari S, Giron A, Marrelec G. et al. Abnormal cortical brain integration of somatosensory afferents in ALS. Clin Neurophysiol. 2018;129(4):874–84.

References

  • Lee H, Gunraj C, Chen R. J Physiol. 2007;580(Pt3):1021–32.
  • Karandreas N, Papadopoulou M, Kokotis P, et al. ALS. 2007;8(2):112–8.

References

  • Brettschneider J, Del Tredici K, Toledo JB, et al. Stages of pTDP-43 pathology in amyotrophic lateral sclerosis. Ann Neurol. 2013;74(1):20–38.
  • Dieckmann N, Roediger A, Prell T, et al. Cortical and subcortical grey matter atrophy in Amyotrophic Lateral Sclerosis correlates with measures of disease accumulation independent of disease aggressiveness. Neuroimage Clin. 2022;36:103162.

Reference

References

References

Reference

References

  • Ceccanti M, Pozzilli V, Cambieri C. et al. Creatine kinase and progression rate in amyotrophic lateral sclerosis. Cells. 2020;9(5):1174.
  • Nijssen J. Motor neuron vulnerability and resistance in amyotrophic lateral sclerosis. Acta Neuropathol. 2017;133(6):863–85.
  • Vogt T. Functional properties of motor units in motor neuron diseases and neuropathies. Electroencephalogr Clin Neurophysiol. 1997;105(4):328–32.

References

  • Swash M. Why are upper motor neuron signs difficult to elicit in amyotrophic lateral sclerosis? J Neurol Neurosurg Psychiatry. 2012;83(6):659–62.
  • Shefner JM, Al-Chalabi A, Baker MR, et al. A proposal for new diagnostic criteria for ALS. Clin Neurophysiol. 2020;131(8):1975–8.
  • Wendebourg MJ, Sander L, Kesenheimer E, et al. The spinal cord lateral tract sign in amyotrophic lateral sclerosis: an rAMIRA based MRI sign for upper motor neuron involvement in a clinical setting. Poster presented at ENCALS; 2022.

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