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Elliot J. Glotfelty

Researcher at National Institutes of Health

Publications -  20
Citations -  323

Elliot J. Glotfelty is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Neuroprotection & Medicine. The author has an hindex of 8, co-authored 15 publications receiving 164 citations. Previous affiliations of Elliot J. Glotfelty include United States Department of the Army & United States Army Medical Research Institute of Chemical Defense.

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Journal ArticleDOI

Structural, morphological, and functional correlates of corneal endothelial toxicity following corneal exposure to sulfur mustard vapor

TL;DR: A model is proposed that explains the relationships among SM dose, the biphasic progression, and the various clinical trajectories of corneal SM injury and that provides a mechanism for temporal variations in MGK onset.
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Glucagon-like peptide-1 (GLP-1)-based receptor agonists as a treatment for Parkinson's disease.

TL;DR: This mini-review describes the development of GLP-1R agonists and their potential therapeutic value in treating Parkinson’s Disease, and presents preclinical data offering insights into the use of monomeric dual- and tri-agonist incretin-based mimetics for neurodegenerative disorders.
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Incretin Mimetics as Rational Candidates for the Treatment of Traumatic Brain Injury

TL;DR: A growing body of literature supports the use of glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic peptide (GIP), and glucagon (Gcg) receptor (R) agonists, along with unimolecular combinations of these therapies, for their potent neurotrophic/neuroprotective activities across a variety of cellular and animal models of chronic neurodegenerative diseases.
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Role of chronic neuroinflammation in neuroplasticity and cognitive function: A hypothesis

TL;DR: Evaluating the efficacy of 3,6'-dithioPomalidomide in 5xFAD Alzheimer's disease mice to test the hypothesis that neuroinflammation is directly involved in the development of synaptic/neuronal loss and cognitive decline is tested.