ParkinsonCanadaV1, PascalFrancis, Corpus, bibRecord, 000069

Source memory in normal aging and Parkinson's disease

Identifieur interne : 000069 ( PascalFrancis/Corpus ); précédent : 000068; suivant : 000070

Source memory in normal aging and Parkinson's disease

Auteurs : Patrick S. R. Davidson ; Shaun P. Cook ; Leslie Mcghan ; Thomas Bouchard ; Richard Camicioli

Source :

Journal of neuropsychology : (Print) [ 1748-6645 ] ; 2013.

RBID : Pascal:13-0320400

Descripteurs français

Pascal (Inist)
- Mémoire, Source information, Sénescence, Maladie de Parkinson, Etude expérimentale, Trouble de la mémoire, Homme.

English descriptors

KwdEn :
- Experimental study, Human, Information source, Memory, Memory disorder, Parkinson disease, Senescence.

Abstract

Several theorists have described memory in Parkinson's disease (PD) as involving an amplification of the deficits seen in normal aging, and drawn parallels between PD and frontal lesion patients. Both normal aging and frontal lobe damage impair memory for the context in which one has encountered information (i.e., source memory). We thus sought to determine whether PD patients would show especially poor source memory. We assessed memory for perceptual (voice), spatial (location of loudspeaker), and temporal (list) source memory in 18 PD patients, 23 healthy older adults, and 35 young people. Although both the healthy aged and PD groups performed more poorly than the young on most of the memory tests, the PD patients failed to show significantly greater impairments than the healthy older adults. The PD patients did perform more poorly, however, on a measure of executive function (the Wisconsin Card Sorting Test [WCST]). We discuss potential reasons why PD had a surprisingly minimal effect on source memory in our study, and relate our data to broader theories of memory impairment in Parkinson's disease.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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Format Inist (serveur)

NO :	PASCAL 13-0320400 INIST
ET :	Source memory in normal aging and Parkinson's disease
AU :	DAVIDSON (Patrick S. R.); COOK (Shaun P.); MCGHAN (Leslie); BOUCHARD (Thomas); CAMICIOLI (Richard); EDELSTYN (Nicky); POLIAKOFF (Ellen)
AF :	School of Psychology, Bruyère Research Institute, Centre for Stroke Recovery, University of Ottawa/Canada (1 aut.); Department of Psychology, Millersville University/Pennsylvania/Etats-Unis (2 aut.); Alberta Hospital/Edmonton/Canada (3 aut.); Glenrose Rehabilitation Hospital/Edmonton/Canada (4 aut., 5 aut.); Department of Medicine (Neurology), University of Alberta/Canada (4 aut., 5 aut.); Keele University/Royaume-Uni (1 aut.); University of Manchester/Royaume-Uni (2 aut.)
DT :	Publication en série; Niveau analytique
SO :	Journal of neuropsychology : (Print); ISSN 1748-6645; Royaume-Uni; Da. 2013; Vol. 7; No. 2; Pp. 179-192; Bibl. 3 p.1/4
LA :	Anglais
EA :	Several theorists have described memory in Parkinson's disease (PD) as involving an amplification of the deficits seen in normal aging, and drawn parallels between PD and frontal lesion patients. Both normal aging and frontal lobe damage impair memory for the context in which one has encountered information (i.e., source memory). We thus sought to determine whether PD patients would show especially poor source memory. We assessed memory for perceptual (voice), spatial (location of loudspeaker), and temporal (list) source memory in 18 PD patients, 23 healthy older adults, and 35 young people. Although both the healthy aged and PD groups performed more poorly than the young on most of the memory tests, the PD patients failed to show significantly greater impairments than the healthy older adults. The PD patients did perform more poorly, however, on a measure of executive function (the Wisconsin Card Sorting Test [WCST]). We discuss potential reasons why PD had a surprisingly minimal effect on source memory in our study, and relate our data to broader theories of memory impairment in Parkinson's disease.
CC :	002B18C13; 002B17G; 002A26J05; 002A26F05A
FD :	Mémoire; Source information; Sénescence; Maladie de Parkinson; Etude expérimentale; Trouble de la mémoire; Homme
FG :	Cognition; Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central; Pathologie du système nerveux; Trouble cognitif
ED :	Memory; Information source; Senescence; Parkinson disease; Experimental study; Memory disorder; Human
EG :	Cognition; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease; Nervous system diseases; Cognitive disorder
SD :	Memoria; Fuente información; Senescencia; Parkinson enfermedad; Estudio experimental; Trastorno memoria; Hombre
LO :	INIST-28032.354000501984320030
ID :	13-0320400

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Pascal:13-0320400

Le document en format XML

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<front><div type="abstract" xml:lang="en">Several theorists have described memory in Parkinson's disease (PD) as involving an amplification of the deficits seen in normal aging, and drawn parallels between PD and frontal lesion patients. Both normal aging and frontal lobe damage impair memory for the context in which one has encountered information (i.e., source memory). We thus sought to determine whether PD patients would show especially poor source memory. We assessed memory for perceptual (voice), spatial (location of loudspeaker), and temporal (list) source memory in 18 PD patients, 23 healthy older adults, and 35 young people. Although both the healthy aged and PD groups performed more poorly than the young on most of the memory tests, the PD patients failed to show significantly greater impairments than the healthy older adults. The PD patients did perform more poorly, however, on a measure of executive function (the Wisconsin Card Sorting Test [WCST]). We discuss potential reasons why PD had a surprisingly minimal effect on source memory in our study, and relate our data to broader theories of memory impairment in Parkinson's disease.</div>
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<s5>03</s5>
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<fC03 i1="03" i2="X" l="SPA"><s0>Senescencia</s0>
<s5>03</s5>
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<fC03 i1="04" i2="X" l="FRE"><s0>Maladie de Parkinson</s0>
<s2>NM</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Parkinson disease</s0>
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<s5>04</s5>
</fC03>
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<s2>NM</s2>
<s5>04</s5>
</fC03>
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<s5>05</s5>
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<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Trouble de la mémoire</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Memory disorder</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Trastorno memoria</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Homme</s0>
<s5>18</s5>
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<s5>18</s5>
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<fC03 i1="07" i2="X" l="SPA"><s0>Hombre</s0>
<s5>18</s5>
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<s5>37</s5>
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<s5>37</s5>
</fC07>
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<s5>37</s5>
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<fC07 i1="02" i2="X" l="FRE"><s0>Pathologie de l'encéphale</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Syndrome extrapyramidal</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Pathologie du   système nerveux central</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Pathologie du   système nerveux</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>42</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Trouble cognitif</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Cognitive disorder</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Trastorno cognitivo</s0>
<s5>43</s5>
</fC07>
<fN21><s1>301</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 13-0320400 INIST</NO>
<ET>Source memory in normal aging and Parkinson's disease</ET>
<AU>DAVIDSON (Patrick S. R.); COOK (Shaun P.); MCGHAN (Leslie); BOUCHARD (Thomas); CAMICIOLI (Richard); EDELSTYN (Nicky); POLIAKOFF (Ellen)</AU>
<AF>School of Psychology, Bruyère Research Institute, Centre for Stroke Recovery, University of Ottawa/Canada (1 aut.); Department of Psychology, Millersville University/Pennsylvania/Etats-Unis (2 aut.); Alberta Hospital/Edmonton/Canada (3 aut.); Glenrose Rehabilitation Hospital/Edmonton/Canada (4 aut., 5 aut.); Department of Medicine (Neurology), University of Alberta/Canada (4 aut., 5 aut.); Keele University/Royaume-Uni (1 aut.); University of Manchester/Royaume-Uni (2 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Journal of neuropsychology : (Print); ISSN 1748-6645; Royaume-Uni; Da. 2013; Vol. 7; No. 2; Pp. 179-192; Bibl. 3 p.1/4</SO>
<LA>Anglais</LA>
<EA>Several theorists have described memory in Parkinson's disease (PD) as involving an amplification of the deficits seen in normal aging, and drawn parallels between PD and frontal lesion patients. Both normal aging and frontal lobe damage impair memory for the context in which one has encountered information (i.e., source memory). We thus sought to determine whether PD patients would show especially poor source memory. We assessed memory for perceptual (voice), spatial (location of loudspeaker), and temporal (list) source memory in 18 PD patients, 23 healthy older adults, and 35 young people. Although both the healthy aged and PD groups performed more poorly than the young on most of the memory tests, the PD patients failed to show significantly greater impairments than the healthy older adults. The PD patients did perform more poorly, however, on a measure of executive function (the Wisconsin Card Sorting Test [WCST]). We discuss potential reasons why PD had a surprisingly minimal effect on source memory in our study, and relate our data to broader theories of memory impairment in Parkinson's disease.</EA>
<CC>002B18C13; 002B17G; 002A26J05; 002A26F05A</CC>
<FD>Mémoire; Source information; Sénescence; Maladie de Parkinson; Etude expérimentale; Trouble de la mémoire; Homme</FD>
<FG>Cognition; Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central; Pathologie du   système nerveux; Trouble cognitif</FG>
<ED>Memory; Information source; Senescence; Parkinson disease; Experimental study; Memory disorder; Human</ED>
<EG>Cognition; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease; Nervous system diseases; Cognitive disorder</EG>
<SD>Memoria; Fuente información; Senescencia; Parkinson enfermedad; Estudio experimental; Trastorno memoria; Hombre</SD>
<LO>INIST-28032.354000501984320030</LO>
<ID>13-0320400</ID>
</server>
</inist>
</record>

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	La maladie de Parkinson au Canada (serveur d'exploration)
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La maladie de Parkinson au Canada (serveur d'exploration)

Source memory in normal aging and Parkinson's disease

Source memory in normal aging and Parkinson's disease

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