Cited by 1,186Memory and Neural MechanismsNeuroscience and Neuropharmacology ResearchNeurogenesis and neuroplasticity mechanisms

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The Hippocampus Book

·2006·Oxford University Press eBooks

DOI 10.1093/acprof:oso/9780195100273.001.0001

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Abstract

Abstract The hippocampus is one of a group of remarkable structures embedded within the brain's medial temporal lobe. Long known to be important for memory, it has been a prime focus of neuroscience research for many years. This book aims to facilitate developments in the field in a major way by bringing together contributions by leading international scientists knowledgeable about hippocampal anatomy, physiology, and function. This book offers an up-to-date account of what the hippocampus does, how it does it, and what happens when things go wrong. At the same time, it illustrates how research focusing on this single brain structure has revealed principles of wider generality for the whole brain in relation to anatomical connectivity, synaptic plasticity, cognition and behavior, and computational algorithms. Well-organized in its presentation of both theory and experimental data, this book illustrates the astonishing progress that has been made in unraveling the workings of the brain.

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“Published by Elsevier Inc a b s t r a c t a r t i c l e i n f o”
Background
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Background
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Venue: Oxford University Press eBooks
Publisher: Oxford University Press
Published: 2006-12-14
DOI: 10.1093/acprof:oso/9780195100273.001.0001
OpenAlex: W644076287
Cited by: 1,186
References: 0
Citations by year: 2026: 15 · 2025: 33 · 2024: 37 · 2023: 32 · 2022: 44 · 2021: 68 · 2020: 71 · 2019: 67 · 2018: 79 · 2017: 66 · 2016: 60 · 2015: 78 · 2014: 91 · 2013: 108 · 2012: 68
FWCI: 12.76
Type: book
Language: en
Open access: closed
Locations: Oxford University Press eBooks (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: hippocampus, medial temporal lobe, memory, hippocampal anatomy, hippocampal dysfunction, synaptic plasticity, structural connectivity, cognition and behavior, computational neuroscience, brain function

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