References
- Bashford J, Wickham A, Iniesta R, et al. Brain Commun. 2020;2(1):fcaa018.
- Bibbings K, Harding PJ, Loram ID, et al. Ultrasound Med Biol. 2019;45:1164–75.
- Planinc D, Muhamood N, Cabassi C, et al. Clin Neurophysiol. 2023;145:71–80.
References
- Bashford J, Wickham A, Iniesta R et al. SPiQE: An automated analytical tool for detecting and characterising fasciculations in amyotrophic lateral sclerosis. Clin Neurophysiol. 2019;130(7):1083–90.
- Bashford J, Wickham A, Iniesta R, et al. Preprocessing surface EMG data removes voluntary muscle activity and enhances SPiQE fasciculation analysis. Clin Neurophysiol. 2020;131(1):265–73.
Reference
- Robertson I, Manly T, Andrade J, et al. `Oops!’: performance correlates of everyday attentional failures in traumatic brain injured and normal subjects. Neuropsychologia. 1997;35(6)747–58.
References
- van Veenhuijzen K, Westeneng HJ, Tan H, et al. Ann Neurol. 2022;93:668–80.
- Dukic S, McMackin R, Buxo T, et al. Human Brain Map. 2019;40:4827–42.
- Nasseroleslami B, Dukic S, Broderick M, et al. Cerebral Cortex. 2019;29:27–41.
Reference
- Neuwirth C, Barkhaus PE, Burkhardt C, Castro J, Czell D, de Carvalho M, Nandedkar S, Stalberg E, Weber M. Motor unit number index (MUNIX) detects motor neuron loss in pre-symptomatic muscles in amyotrophic lateral sclerosis. Clin Neurophysiol. 2017;128(3):495–500
References
- Brettschneider J, Del Tredici K, Toledo JB, et al. Stages of pTDP-43 pathology in amyotrophic lateral sclerosis. Ann Neurol. 2013;74:20–38.
- Bertoux M, O'Callaghan C, Flanagan E, et al. Fronto-striatal atrophy in behavioral variant frontotemporal dementia and Alzheimer's disease. Front Neurol. 2015;6:147.
Reference
- 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
- Vucic S, Ziemann U, Eisen A, et al. J Neurol Neurosurg Psychiatry 2013;84:1161–70.
- Sangari S, Iglesias C, El Mendili M. et al. Clin Neurophysiol. 2016;127(4):1968–77.
- Lackmy-Vallee A, Giboin L.-S., Marchand-Pauvert V. et al. Eur J Neurosci. 2012;35:457–67.
- Kujirai T, Caramia MD, Rothwell JC. et al. J Physiol. 1993;471:501–19.
- Lackmy A, Marchand-Pauvert V. Clin Neurophysiol. 2010;121:612–21
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
- Yu X, Ji C, Shao A. Neurovascular unit dysfunction and neurodegenerative disorders. Front Neurosci. 2020;14:334.
References
- Vucic S, Kiernan M, Handbook Clin Neurol, 2013;116:561–75.
- Grandjean J., Quoilin C., Duque J. Neurophysiologie Clinique. 2018;49(2): 137–47.
References
- Garand KL, Schwertner R, Chen A, et al. Dysphagia. 2018;33:243–50.
- Re GL, Terranova MC, Vernuccio F, et al. Pol J Radiol. 2018;83:e394–400.
Reference
- Hobson-Webb LD, Simmons Z. Muscle Nerve. 60(2):114–123.
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.