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Arnold S. Lippa

Researcher at New York University

Publications -  11
Citations -  5551

Arnold S. Lippa is an academic researcher from New York University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 3, co-authored 3 publications receiving 5304 citations. Previous affiliations of Arnold S. Lippa include American Cyanamid.

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The Cholinergic Hypothesis of Geriatric Memory Dysfunction

TL;DR: Biochemical, electrophysiological, and pharmacological evidence supporting a role for cholinergic dysfunction in age-related memory disturbances is critically reviewed and an attempt has been made to identify pseudoissues, resolve certain controversies, and clarify misconceptions that have occurred in the literature.
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Animal tests of anxiety

TL;DR: This unit presents protocols for the most commonly used animal tests of anxiety, including the Geller‐Seifter conflict test, the social interaction test, light/dark exploration, the elevated plus‐maze, defensive burying, and the thirsty rat conflict.
Journal ArticleDOI

Animal Tests of Anxiety

TL;DR: This unit presents protocols for the most commonly used animal tests of anxiety, including the Geller‐Seifter conflict test, the social interaction test, light/dark exploration, the elevated plus‐maze, defensive burying, and the thirsty rat conflict.
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The imidazodiazepine, KRM-II-81: An example of a newly emerging generation of GABAkines for neurological and psychiatric disorders

TL;DR: KRM-II-81 is the lead compound in a new series of orally bioavailable imidazodiazepines entering IND-enabling safety studies as discussed by the authors , which has a preclinical profile predicting efficacy against pharmacoresistant epilepsy, traumatic brain injury, and neuropathic pain.
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Metabolism, pharmacokinetics, and anticonvulsant activity of a deuterated analog of the α2/3‐selective GABAkine KRM‐II‐81

TL;DR: D5‐K RM‐II‐81, like KRM‐II-81, significantly prevented seizures induced by pentylenetetrazol when given orally and was targeted in the design of a deuterated analog that could be evaluated as a potentially longer‐acting analog.