The changing scene of amyotrophic lateral sclerosis
By W. Robberecht, T. Philips. Nature Reviews Neuroscience, 2013
966 citations recorded by the source corpus.
Subfields: Neurology
View Paper: https://www.semanticscholar.org/paper/06c70801a5d8883a9899a511e13a7f9913126419
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Neurology
- Henrik Zetterberg
- David M. Wilson
- M. Cookson
- Robert H. Brown
- D. Holtzman
- L. Van Den Bosch
- Clifford J. Woolf
- I. Dewachter
Citations in the corpus
- Intrinsic Membrane Hyperexcitability of ALS Patient-Derived Motor Neurons (2014, background): “, 2014), which is responsible for 40%–50% of familial ALS and approximately 10% of sporadic cases (Robberecht and Philips, 2013).”
- Superoxide dismutases: Dual roles in controlling ROS damage and regulating ROS signaling (2018, neutral): “Altered SOD expression or activity changes are observed in various pathological conditions such as, for example, cancer and amyotropic lateral sclerosis (ALS; Dhar and St Clair, 2012; Robberecht and Philips, 2013).”
- Hallmarks of neurodegenerative diseases. (2023, positive): “28,44,53,54,56,57,65 Mislocalized TDP-43, which functions as an RNA-binding protein, causes altered RNA splicing, RNA stability, and RNA transport.”