Stages of pTDP‐43 pathology in amyotrophic lateral sclerosis

By J. Brettschneider, K. Del Tredici, J. Toledo, John L. Robinson, D. Irwin, Murray C. Grossman, Eunran Suh, V. Deerlin, E. Wood, Young Baek and 10 more. Annals of Neurology, 2013

986 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Neurology

View Paper: https://www.semanticscholar.org/paper/cf4da61cc8dac23816bcd5ee55fd24c23827ec8e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cellular and Molecular Neuroscience

1. Dennis W. Dickson
2. Reisa A. Sperling
3. John Q. Trojanowski
4. Clifford R. Jack Jr.
5. Peter T. Nelson
6. William W. Seeley

In Neurology

1. Dennis W. Dickson
2. Brittany N. Dugger
3. Helena Chui
4. Julie A. Schneider
5. Reisa A. Sperling
6. John Q. Trojanowski
7. Clifford R. Jack Jr.
8. William W. Seeley

Citations in the corpus

• Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report (2019, background): “This does not address regions that would be assessed in separate TDP-43 pathological staging schemes developed for ALS or FTLD-TDP (Brettschneider et al., 2013; Fatima et al., 2015; Tan et al., 2015; Verde et al., 2017; Neumann and Mackenzie, 2019).”
• Pathology of Neurodegenerative Diseases. (2017, background): “Although motor neurons are most vulnerable, there is spread of the pathology to extramotor sites (e.g., hippocampus, amygdala, and cortex) in cases with longstanding disease or in those with dementia (Brettschneider et al. 2013).”