Cited by 892Memory and Neural MechanismsMemory Processes and InfluencesNeural and Behavioral Psychology Studies

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A triple dissociation of memory systems: Hippocampus, amygdala, and dorsal striatum.

McDonald, Robert J., White, Norman M.·1993·Behavioral Neuroscience

DOI 10.1037/0735-7044.107.1.3

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The basal ganglia.
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Authors: McDonald, R. J., & White, N. M.
ORCID: McDonald, Robert J.
White, Norman M.
Venue: Behavioral Neuroscience
Publisher: American Psychological Association (APA)
Published: 1993
Volume: 107
Issue: 1
Pages: 3-22
ISSN: 0735-7044 (ISSN-L)
1939-0084
DOI: 10.1037/0735-7044.107.1.3
OpenAlex: W4232217111
Cited by: 885
References: 0
Citations by year: 2025: 4 · 2024: 5 · 2023: 18 · 2022: 12 · 2021: 18 · 2020: 53 · 2019: 19 · 2018: 31 · 2017: 35 · 2016: 40 · 2015: 34 · 2014: 25 · 2013: 33 · 2012: 23
FWCI: 9.82
Type: journal article
Language: en
Open access: closed
Locations: Behavioral Neuroscience (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords: memory systems, hippocampus, amygdala, dorsal striatum, memory dissociation

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A triple dissociation of memory systems: Hippocampus, amygdala, and dorsal striatum.

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