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2 results are consistent with the notion that declarative and habit learning compete to mediate task p
5 al predictor of performance on memory tasks (declarative and nondeclarative) than previously thought.
7 eral CPU, or control lesions were trained on declarative and procedural knowledge variants of a novel
8 uning of corticostriatal systems involved in declarative and procedural learning, a capacity potentia
9 eep's capacity to boost the consolidation of declarative and procedural memories, nor sleep's quality
11 ning or injury; second, the knowledge of how declarative and procedural memory operates and how this
13 which are regions assumed to play a role in declarative and procedural memory, provides an anatomica
15 rom multiple cognitive domains, particularly declarative and working memory and executive function.
16 odulate the engagement of hippocampus-based "declarative" and striatum-based "procedural" memory syst
17 ippocampus, a structure involved in spatial, declarative, and contextual memory, after seizures or is
21 during consolidation, impairment of the fast/declarative component leads to improvements in the slow/
23 targeting the pathologic emotional, but not declarative, component of a memory would be ideal for cl
24 ay abolish the pathologic emotional, but not declarative, component of memories allowing alleviation
25 information, which is ordinarily learned as declarative (conscious) knowledge and with the participa
26 al temporal lobe memory system that supports declarative (conscious) memory; and (iii) in humans, bil
27 ment, the reciprocal relationship was found: declarative consolidation was blocked by procedural lear
29 Neural circuits associated with motivated declarative encoding and active threat avoidance have bo
30 ber of disorders, accompanied by deficits in declarative episodic, spatial, and contextual memory per
31 res of processing speed, working memory, and declarative (facial) memory as candidate endophenotypes
33 ntly, the relationship between awareness and declarative (hippocampus-dependent) memory has been ques
34 human data supporting a benefit of sleep for declarative (hippocampus-mediated) memory in humans (for
35 amidal cells are less critically involved in declarative human memory acquisition compared to dentate
37 their WT littermates in situations in which declarative (i.e., place-based) and procedural (i.e., re
38 for developers as well as a straightforward declarative interface that lets users easily share and e
39 a translational schema for NLP that contains declarative knowledge about genes and their associated b
41 ity was correlated with task performance and declarative knowledge after learning under single-task c
43 e importance of considering the influence of declarative knowledge when interpreting age-associated c
44 he latter, including functions as diverse as declarative knowledge, episodic memory, word learning, a
45 ion is thought to require overt reasoning on declarative knowledge, namely, on facts pertaining to pr
50 association of top-down signals relevant for declarative learning and spatially precise ascending tac
51 t cells in the hippocampus appear to support declarative learning by distinguishing novel and familia
52 findings further suggest a brain system for declarative learning motivated by punishment that is dis
53 e motor skill improvement, can be blocked by declarative learning over wake, but not over a night of
54 cits in dyslexia are attributed to an intact declarative learning system combined with an impaired pr
61 in S-R learning from those of a cognitive or declarative medial temporal lobe memory system that incl
62 e refuting the hypothesis that procedural or declarative memories are processed/consolidated in sleep
65 hanisms can be recruited to prevent unwanted declarative memories from entering awareness, and that t
66 rst study to demonstrate that sleep protects declarative memories from subsequent associative interfe
67 during sleep may facilitate the transfer of declarative memories from the hippocampus to the neocort
71 mation critical for establishing spatial and declarative memories will benefit greatly from determini
72 n, a process that enables the flexibility of declarative memories, are both hippocampus-dependent and
73 are essential for the formation of long-term declarative memories, both spatial and non-spatial, but
74 lly known for its role in building long-term declarative memories, enables the spread of value across
77 nown as consolidation, which, in the case of declarative memories, occurs within the medial temporal
85 or-word subscale score) as well as in verbal declarative memory (as measured by the Paragraph Recall
86 ly related structures that are essential for declarative memory (conscious memory for facts and event
87 on have deficits in hippocampal-based verbal declarative memory (e.g., recall of a paragraph) and in
88 ed to identify the neuroanatomy of long-term declarative memory (sometimes termed explicit memory).
90 ocessing (the paced serial addition task) or declarative memory (the delayed paragraph recall task),
92 1.48; 95% CI, 1.08-2.04; P = .02), impaired declarative memory abilities (beta = -0.87; HR, 0.42; 95
93 n attention and working memory abilities and declarative memory abilities (Cohen d, approximately 0.8
94 n attention and working memory abilities and declarative memory abilities, is a robust characteristic
97 approaches to the treatment of psychosis and declarative memory alterations and in novel animal prepa
99 sm for substantial normal variation in human declarative memory and suggest that the basic effects of
100 The hippocampus is crucial for episodic or declarative memory and the theta rhythm has been implica
104 motivation has been demonstrated to enhance declarative memory by facilitating systems-level consoli
105 hypothesis that circadian arrhythmia impairs declarative memory by increasing the relative influence
106 cortical acetylcholine in a rodent model of declarative memory by infusing the cholinergic muscarini
108 Type 3, n = 5) showed significantly reduced declarative memory capacities (intracarotid amobarbital
109 view that the hippocampus mediates a general declarative memory capacity in animals, as it does in hu
111 Alzheimer's disease (AD), the impairment of declarative memory coincides with the accumulation of ex
114 s followed by an improved procedural but not declarative memory consolidation under conditions of SD.
116 Individuals with T2DM had specific verbal declarative memory deficits, reduced hippocampal and pre
119 nce for hippocampal involvement in long-term declarative memory encoding and for the view that the am
120 campal region and the amygdala, in long-term declarative memory encoding was examined by using positr
121 e imaging in humans to examine mechanisms of declarative memory enhancement when subjects were motiva
123 hat the medial temporal lobe (MTL) subserves declarative memory exclusively, whereas nondeclarative m
125 a is involved with the formation of enhanced declarative memory for emotionally arousing events.
128 al stimulation to the amygdala could enhance declarative memory for specific images of neutral object
130 ars to have a complex influence on long-term declarative memory for those stimuli: Whereas emotion en
131 hese two processes are related in supporting declarative memory formation and how they are compromise
132 view that the amygdala is not involved with declarative memory formation for nonemotional material.
135 ols; (3) that hippocampal volumes and verbal declarative memory function will be positively correlate
136 associational activity in CA3, with degraded declarative memory function, and with formation of false
137 on are consistently reported; impairments in declarative memory function, especially in the flexible
138 The temporal lobes play a prominent role in declarative memory function, including episodic memory (
139 ed the nature and recovery of procedural and declarative memory functioning in a cocaine-abusing coho
144 premise that the amygdala causally enhances declarative memory has not been directly tested in human
145 l loss (HS ILAE Type 2; n = 13) did not show declarative memory impairment and were indistinguishable
147 et) substitution is associated with impaired declarative memory in healthy volunteers and patients wi
152 , the idea that MTL components contribute to declarative memory in similar ways has also been contrad
154 ongest arguments against a role for sleep in declarative memory involves the demonstration that the m
160 One of the most widely studied examples of declarative memory is the capacity to recognize recently
164 cortical regions was associated with better declarative memory only in bipolar disorder subjects, an
166 onance imaging was used with a simple visual declarative memory paradigm to test for differences in n
167 inding is minimized, showing that relational/declarative memory per se is not impaired in aging.
176 wo functions of the fronto-parietal network: declarative memory retrievals and updating of working me
178 igm is a particularly good system to explore declarative memory since humans do not acquire trace con
179 gdala is not a site of long-term explicit or declarative memory storage, but serves to influence memo
180 sentation of the trauma in the context-based declarative memory system in favor of its overrepresenta
182 ask the benefits of sleep by challenging the declarative memory system with competing information (in
183 a significant limitation on the hippocampal declarative memory system, and impaired interference man
184 rovide evidence for an interaction between a declarative memory system, dependent on the medial tempo
188 al evidence suggests prolonged maturation of declarative memory systems in the human brain from child
190 detrimental effect on a sensitive nonverbal declarative memory task in cocaine-dependent subjects fo
192 l functioning during performance of a verbal declarative memory task in subjects with midlife major d
194 left dorsolateral prefrontal cortex during a declarative memory task involving learning a set of word
196 onal magnetic resonance imagery responses of declarative memory tasks in the medial temporal lobe (MT
197 sia, however, have shown that performance on declarative memory tasks may not always be dependent on
198 the performance of hippocampal-based verbal declarative memory tasks was measured by using positron
199 re separated in time and may make demands on declarative memory that are beyond the capacity of amnes
200 l-process theory predicts no effect, whereas declarative memory theory predicts impairment of all typ
201 The latter finding is incompatible with declarative memory theory, whereas the former constrains
202 maturation of the neural systems supporting declarative memory to assess the necessity of early memo
204 These findings not only demonstrate enhanced declarative memory when individuals have perceived contr
205 executive" functions, and some components of declarative memory with aging, most studies have failed
206 dose produced reversible decreases in verbal declarative memory without effects on nonverbal memory,
208 pisodic and semantic memory (together termed declarative memory) is an unresolved and much-debated to
210 they support the link between aware memory, declarative memory, and hippocampus-dependent memory.
211 d tests of processing speed, working memory, declarative memory, and intelligence, no evidence for pl
212 sitively correlated with psychosis severity, declarative memory, and overall cognitive performance (P
214 emporal lobe damage impairs the formation of declarative memory, and that semantic knowledge is impai
215 esponse to altered scenes reflect conscious, declarative memory, and they support the link between aw
216 s, but the extent to which animals also have declarative memory, and whether inferential expression o
217 temporal lobes are known to be critical for declarative memory, at present the neural mechanisms sup
218 Performance was examined for tests of verbal declarative memory, attention, and executive function.
219 a newly learned rule makes heavy demands on declarative memory, but after thousands of repetitions r
220 mory can be disrupted by a task that engages declarative memory, but the slow motor memory is immune
221 emporal lobe structures are known to support declarative memory, but there is not consensus about wha
222 mpus dependent because, as in other tasks of declarative memory, conscious knowledge must be acquired
223 ial temporal lobe (MTL), a critical area for declarative memory, have been shown to change their tuni
224 th lower scores on measures of attention and declarative memory, including several measures of audito
225 e relationship between the basal ganglia and declarative memory, including the involvement of striatu
226 rast, showed more specific associations with declarative memory, letter fluency and processing speed
228 nitary memory system supporting all types of declarative memory, our conscious memory for facts and e
229 The hippocampus is critical for encoding declarative memory, our repository of knowledge of who,
230 depression) on general intellectual ability, declarative memory, procedural memory, executive functio
231 tive performance scores, executive function, declarative memory, processing speed, or visuoperception
232 ests could be summarized as four constructs: declarative memory, signal discrimination, working memor
234 ppocampus plays a broad role in episodic and declarative memory, whereas others argue for a specific
235 nts derives from their general impairment in declarative memory, which affects performance on most 2-
236 The findings support the distinction between declarative memory, which depends on the hippocampus and
237 hought to operate together in the service of declarative memory--memory for facts and events--having
238 The hippocampus serves a critical role in declarative memory--our capacity to recall everyday fact
239 n function that may use such interactions is declarative memory--that is, memory that can be consciou
240 memory consolidates in a manner analogous to declarative memory--that is, with the formation of a mem
241 aration reveals action-independent coding of declarative memory-based familiarity and confidence of c
269 a causal link between these two features of declarative memory: Temporal binding is a necessary cond
271 ppocampal region of the brain is crucial for declarative or episodic memory for a broad range of mate
274 g depending upon whether the task emphasized declarative or nondeclarative memory, even when the to-b
275 ort of incidental/observational learning in "declarative" or "episodic" memory versus the striatal su
276 fewer instances of word use, vocalizations, declarative pointing, social gaze, and orienting to name
279 ible expression, indicating that non-spatial declarative processing depends specifically on the hippo
282 f reconsolidation-updating theory by using a declarative recall task and sequences similar to phone n
284 icated the hippocampal formation in spatial, declarative/relational and episodic types of memory.
286 e subject (S), verb (V), and object (O) in a declarative sentence of the type "the man (S) killed (V)
288 ed learning strategy from a single-cue-based declarative strategy to a multicue-based procedural stra
293 pal formation participates in acquisition of declarative tasks but is not the site of their long-term
295 form of FOXP2 promotes faster switching from declarative to procedural learning strategies when the t
298 xia syndrome-affected participants with poor declarative verbal memory would have pronounced abnormal
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