Autonomic dysfunction in amyotrophic lateral sclerosis: A neurophysiological and neurosonology study
Journal of Neuroimaging2022Vol. 32(4), pp. 710–719
Citations Over TimeTop 10% of 2022 papers
Μarianna Papadopoulou, Eleni Bakola, Απόστολος Παπαποστόλου, Maria‐Ioanna Stefanou, Christos Moschovos, Stavroula Salakou, Panagiotis Zis, Vasiliki Zouvelou, Vasilios Κ. Kimiskidis, Elisabeth Chroni, Georgios Tsivgoulis
Abstract
This study confirms the presence of autonomic dysfunction in ALS patients and provides evidence of VN atrophy that correlates with disease severity and duration and is independent of bulbar involvement. Degeneration of dorsal nucleus neurons of the VN is hypothesized.
Related Papers
- → Progressive Muskelatrophie(2007)7 cited
- [Lower motor neuron diseases with predominantly upper limbs affection: are they independent forms or atypical variants of amyotrophic lateral sclerosis?].(2006)
- Oral Care of a Patient with Amyotrophic Lateral Sclerosis (ALS)(2018)
- → Predictors of survival in amyotrophic lateral sclerosis(2007)
- → Diagnosis and classification of motor neuron disease(2019)