The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Genetic Classification of Primary Neurodegenerative Disease
Abstract
During the past 10 years (the “decade of the brain”), some of the genetic causes of many of the primary neurodegenerative diseases, which include Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, prion disease, and many ataxic syndromes, have been found. These breakthroughs mean that for many of these diseases we now know the initiating trigger as well as the final outcome. These diseases have many pathological mechanisms in common, and there may be relatively few pathways to neuronal death seen in these disorders. Thus, treatment strategies developed for a particular disease may be found to have efficacy in more than one disorder.
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Cited by
Antioxidant enzymes and human diseases
MatÉs, J. M., Pérez-Gómez, C., & De Castro, I. N. (1999) · Clinical Biochemistry · doi:10.1016/s0009-9120(99)00075-2 · Cited by 2,099
Unfolding the role of protein misfolding in neurodegenerative diseases
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Oligomeric and fibrillar species of amyloid-β peptides differentially affect neuronal viability
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Metadata
- Authors
- Hardy, J., & Gwinn-Hardy, K.
- Venue
- Science
- Published
- 1998-11-06
- Volume
- 282
- Issue
- 5391
- Pages
- 1075-1079
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2153536347
- Cited by
- 343
- References
- 18
- FWCI
- 18.87
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
