Dopaminergic system and dream recall: an MRI study in Parkinson's disease patients
Open accessAbstract
We investigated the role of the dopamine system [i.e., subcortical-medial prefrontal cortex (mPFC) network] in dreaming, by studying patients with Parkinson's Disease (PD) as a model of altered dopaminergic transmission. Subcortical volumes and cortical thickness were extracted by 3T-MR images of 27 PD patients and 27 age-matched controls, who were asked to fill out a dream diary upon morning awakening for one week. PD patients do not substantially differ from healthy controls with respect to the sleep, dream, and neuroanatomical measures. Multivariate correlational analyses in PD patients show that dopamine agonist dosage is associated to qualitatively impoverished dreams, as expressed by lower bizarreness and lower emotional load values. Visual vividness (VV) of their dream reports positively correlates with volumes of both the amygdalae and with thickness of the left mPFC. Emotional load also positively correlates with hippocampal volume. Beside the replication of our previous finding on the role of subcortical nuclei in dreaming experience of healthy subjects, this represents the first evidence of a specific role of the amygdala-mPFC dopaminergic network system in dream recall. The association in PD patients between higher dopamine agonist dosages and impoverished dream reports, however, and the significant correlations between VV and mesolimbic regions, however, provide an empirical support to the hypothesis that a dopamine network plays a key role in dream generation. The causal relation is however precluded by the intrinsic limitation of assuming the dopamine agonist dosage as a measure of the hypodopaminergic state in PD. Periodicals, Inc.
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Many afferent and efferent fibers of the posterior and anterior dream systems are connected with the limbic system.
“many of the afferent and efferent fibers of these two systems are connected with the limbic system”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as De Gennaro et al., 2016
The Introduction (page unavailable) says the medial prefrontal cortex connects directly and indirectly to the hippocampus and amygdala, supporting a connection for one of the discussed systems. The Discussion (page unavailable) distinguishes the posterior temporoparietal system from the mesolimbic system, but does not say that afferent and efferent fibers of both systems connect with the limbic system. (LLM, conf=0.82)
Experimental — accuracy not yet measuredThe ventromesial frontal white matter takes part in the interplay between basal forebrain and limbic structures.
“the ventromesial frontal white matter seems to take a part in the interplay between basal forebrain and limbic structures”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as De Gennaro et al., 2016
The Introduction (page unavailable) describes connections between the medial prefrontal cortex and the hippocampus and amygdala. The Discussion (page unavailable) identifies dopaminergic projections in ventromedial frontal white matter and separately discusses basal-forebrain lesions, but does not establish that this white matter mediates an interplay between the basal forebrain and limbic structures. (LLM, conf=0.77)
Experimental — accuracy not yet measuredRecent findings on Parkinson's Disease confirmed an essential interplay between the mPFC and mesolimbic-dopamine system for dreaming.
“the recent findings on PD confirmed the evidence of an essential interplay between the mPFC and mesolimbic-dopamine system for dreaming”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as De Gennaro et al., 2016
The Abstract and Discussion report associations between dream-report features, mPFC thickness, amygdala volume, and dopamine agonist dosage in patients with Parkinson’s disease. The authors call this empirical support for a dopamine network’s role in dreaming, but say a causal relation cannot be established. The claim’s language of a confirmed, essential interplay overstates that evidence. (LLM, conf=0.87)
Experimental — accuracy not yet measuredAccording to the paralimbic hypothesis, emotional salience of dream imagery is due to the activation of the paralimbic cortices by the amygdala, while bizarreness of dream contents is a consequence of prefrontal deactivation, reducing the higher order control on amygdalar and hippocampal functioning.
“According to this hypothesis, emotional salience of dream imagery is due to the activation of the paralimbic cortices by the amygdala,87,88 while bizarreness of dream contents is a consequence of prefrontal deactivation, reducing the higher order control on the amygdalar and hippocampal functioning.110”
From Spotlight on dream recall: the ages of dreams (2018) · cites this paper as [88]
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredLower bizarreness and lower emotional load have been found in Parkinson's disease patients with a hypodopaminergic state.
“At the same time, lower bizarreness and lower emotional load has been found in Parkinson’s disease (PD) patients with a hypodopaminergic state.”
From Spotlight on dream recall: the ages of dreams (2018) · cites this paper as [88]
Parkinson's Disease patients did not differ from healthy subjects with respect to sleep and dream characteristics or neuroanatomical measures.
“PD patients did not differ from healthy subjects with respect to sleep and dream characteristics or the neuroanatomical measures”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as De Gennaro et al., 2016
Higher dopamine agonist dosage is associated with qualitatively impoverished dream experience, as indicated by reduced bizarreness and emotional load levels.
“higher dopamine agonist dosage was associated with qualitatively impoverished DE, as indicated by reduced bizarreness and emotional load levels”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as De Gennaro et al., 2016
Vividness in dream experience is related to the amygdalae and the thickness of the left mPFC.
“confirming that vividness is related to the amygdalae and also the thickness of the left mPFC”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as De Gennaro et al., 2016
Emotional load is positively correlated with hippocampal volume, suggesting a role of the amygdala-mPFC dopaminergic network system in dream recall.
“while emotional load is positively correlated with hippocampal volume, suggesting a role of amygdala–mPFC dopaminergic network system in dream recall.88”
From Spotlight on dream recall: the ages of dreams (2018) · cites this paper as [88]
Visual vividness has been found to positively correlate with the volume of amygdala and the thickness of the left medial prefrontal cortex in Parkinson's disease patients.
“Visual vividness has been found to positively correlate with the volume of amygdala and the thickness of the left medial prefrontal cortex (mPFC) in PD patients”
From Spotlight on dream recall: the ages of dreams (2018) · cites this paper as [88]
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Cites
Folstein, M. F., Folstein, S. E., & McHugh, P. R. (1975) · Journal of Psychiatric Research · doi:10.1016/0022-3956(75)90026-6 · Cited by 88,282 · see citing works
Hirono, N., Mori, E., Ikejiri, Y., Imamura, T., Shimomura, T., Hashimoto, M., Yamashita, H., & Ikeda, M. (1997) · PubMed · Cited by 21,010 · see citing works
Kok, J. S., Berg, I. J., & Scherder, E. J. A. (2013) · Dementia and Geriatric Cognitive Disorders Extra · doi:10.1159/000353441 · Cited by 20,589 · see citing works
Older Adults' Reasons for Using Technology while Aging in Place
Peek, S. T. M., Luijkx, K. G., Rijnaard, M. D., Nieboer, M. E., van der Voort, C. S., Aarts, S., van Hoof, J., Vrijhoef, H. J., & Wouters, E. (2015) · Gerontology · doi:10.1159/000430949 · Cited by 19,803 · see citing works
Sensitivity and False Alarm Rate of a Fall Sensor in Long-Term Fall Detection in the Elderly
Kangas, M., Korpelainen, R., Vikman, I., Nyberg, L., & Jämsä, T. J. (2014) · Gerontology · doi:10.1159/000362720 · Cited by 19,003 · see citing works
Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR)
American Psychiatric Association (2000) · doi:10.1176/appi.books.9780890423349 · Cited by 11,069 · see citing works
Cortical Surface-Based Analysis
Dale, A. M., Fischl, B., & Sereno, M. I. (1999) · NeuroImage · doi:10.1006/nimg.1998.0395 · Cited by 10,910 · see citing works
Staging of brain pathology related to sporadic Parkinson’s disease
Braak, H., Tredici, K. D., Rüb, U., de Vos, R. A. I., Jansen Steur, E. N. H., & Braak, E. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00065-9 · Cited by 10,777 · see citing works
Hughes, A. J., Daniel, S. E., Kilford, L., & Lees, A. J. (1992) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.55.3.181 · Cited by 10,378 · see citing works
Fischl, B., Salat, D. H., Busa, E., Albert, M., Dieterich, M., Haselgrove, C., van der Kouwe, A., Killiany, R., Kennedy, D., Klaveness, S., et al. (2002) · Neuron · doi:10.1016/s0896-6273(02)00569-x · Cited by 8,610 · see citing works
What's wrong with Bonferroni adjustments
Perneger, T. V. (1998) · BMJ · doi:10.1136/bmj.316.7139.1236 · Cited by 5,900 · see citing works
Measuring the thickness of the human cerebral cortex from magnetic resonance images
Fischl, B. R., & Dale, A. M. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.200033797 · Cited by 5,789 · see citing works
Automatically Parcellating the Human Cerebral Cortex
Fischl, B. R. (2003) · Cerebral Cortex · doi:10.1093/cercor/bhg087 · Cited by 4,208 · see citing works
Clinical diagnostic criteria for dementia associated with Parkinson’s disease
Emre, M., Aarsland, D., Brown, R., Burn, D. J., Duyckaerts, C., Mizuno, Y., Broe, G. A., Cummings, J., Dickson, D. W., Gauthier, S., et al. (2007) · Movement Disorders · doi:10.1002/mds.21507 · Cited by 3,027 · see citing works
Carlesimo, G. A., Caltagirone, C., Gainotti, G., Fadda, L., Gallassi, R., Lorusso, S., Marfia, G. A., Marra, C., Nocentini, U., & Parnetti, L. (2008) · European Neurology · doi:10.1159/000117297 · Cited by 1,234 · see citing works
Self-citationFunctional neuroanatomy of human rapid-eye-movement sleep and dreaming
Maquet, P., Péters, J.-M., Aerts, J., Delfiore, G., Degueldre, C., Luxen, A., & Franck, G. (1996) · Nature · doi:10.1038/383163a0 · Cited by 1,168 · see citing works
The cognitive neuroscience of sleep: neuronal systems, consciousness and learning
Hobson, J. A., & Pace-Schott, E. F. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn915 · Cited by 835 · see citing works
Burton, E. J. (2004) · Brain · doi:10.1093/brain/awh088 · Cited by 643 · see citing works
Validity of the Italian Version of the Pittsburgh Sleep Quality Index (PSQI)
Curcio, G., Tempesta, D., Scarlata, S., Marzano, C., Moroni, F., Rossini, P. M., Ferrara, M., & Gennaro, L. D. (2012) · Neurological Sciences · doi:10.1007/s10072-012-1085-y · Cited by 604 · see citing works
Self-citationDreaming and REM sleep are controlled by different brain mechanisms
Solms, M. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00003988 · Cited by 595 · see citing works
Pont‐Sunyer, C., Hotter, A., Gaig, C., Seppi, K., Compta, Y., Katzenschlager, R., Mas, N., Hofeneder, D., Brücke, T., Bayés, A., et al. (2015) · Movement Disorders · doi:10.1002/mds.26077 · Cited by 511 · see citing works
Costafreda, S. G., Fu, C. H. Y., Lee, L., Everitt, B., Brammer, M. J., & David, A. S. (2006) · Human Brain Mapping · doi:10.1002/hbm.20221 · Cited by 496 · see citing works
Magnetic resonance imaging markers of Parkinson's disease nigrostriatal signature
Péran, P., Cherubini, A., Assogna, F., Piras, F., Quattrocchi, C., Peppe, A., Celsis, P., Rascol, O., Démonet, J.-F., Stefani, A., et al. (2010) · Brain · doi:10.1093/brain/awq212 · Cited by 399 · see citing works
Self-citationLéna, I., Parrot, S., Deschaux, O., Muffat‐Joly, S., Sauvinet, V., Renaud, B., Suaud‐Chagny, M. ‐., & Gottesmann, C. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20602 · Cited by 322 · see citing works
The amygdala and medial prefrontal cortex: partners in the fear circuit
Marek, R., Strobel, C., Bredy, T. W., & Sah, P. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.248575 · Cited by 304 · see citing works
Dahan, L., Astier, B., Vautrelle, N., Urbain, N., Kocsis, B., & Chouvet, G. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301251 · Cited by 289 · see citing works
Dreaming as mind wandering: evidence from functional neuroimaging and first-person content reports
Fox, K. C. R., Nijeboer, S., Solomonova, E., Domhoff, G. W., & Christoff, K. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00412 · Cited by 289 · see citing works
Cerebral atrophy and its relation to cognitive impairment in Parkinson disease
Nagano‐Saito, A., Washimi, Y., Arahata, Y., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000149510.41793.50 · Cited by 284 · see citing works
(1997) · Cited by 270 · see citing works
Pfefferbaum, A., Rohlfing, T., Rosenbloom, M. J., Chu, W., Colrain, I. M., & Sullivan, E. V. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.008 · Cited by 256 · see citing works
Nausieda, P. A., Weiner, W. J., Kaplan, L. R., Weber, S., & Klawans, H. L. (1982) · Clinical Neuropharmacology · doi:10.1097/00002826-198205020-00003 · Cited by 245 · see citing works
The roles of the reward system in sleep and dreaming
Perogamvros, L., & Schwartz, S. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.05.010 · Cited by 239 · see citing works
Structural Brain Changes in Parkinson Disease With Dementia
Summerfield, C., Junqué, C., TOLOSA, E. S., Salgado‐Pineda, P., Gómez‐Ansón, B., Martı́, M. J., Pástor, P., Ramírez‐Ruiz, B., & Mercader, J. (2005) · Archives of Neurology · doi:10.1001/archneur.62.2.281 · Cited by 228 · see citing works
Zelikowsky, M., Hersman, S., Chawla, M. K., Barnes, C. A., & Fanselow, M. S. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3624-13.2014 · Cited by 216 · see citing works
REM and NREM sleep reports: comparison of word frequencies by cognitive classes
Antrobus, J. (1983) · Psychophysiology · doi:10.1111/j.1469-8986.1983.tb03015.x · Cited by 215 · see citing works
What are the memory sources of dreaming?
Nielsen, T. A., & Stenstrom, P. (2005) · Nature · doi:10.1038/nature04288 · Cited by 208 · see citing works
Feldmann, Á., Illés, Z., Kosztolányi, P., Illes, E., Mike, A., Kövér, F., Balás, I., Kovács, N., & Nagy, F. T. (2007) · Movement Disorders · doi:10.1002/mds.21765 · Cited by 182 · see citing works
The Neuropsychology of Dreams: A Clinico-Anatomical Study
Pace-Schott, E. F., & Hobson, J. A. (1998) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(98)01166-8 · Cited by 164 · see citing works
Messina, D., Cerasa, A., Condino, F., Arabia, G., Novellino, F., Nicoletti, G., Salsone, M., Morelli, M., Lanza, P. L., & Quattrone, A. (2011) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2010.12.010 · Cited by 163 · see citing works
Pinter, M. M., Pogarell, O. M., & Oertel, W. H. (1999) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.66.4.436 · Cited by 155 · see citing works
Price, S. L., Paviour, D. C., Scahill, R. I., Stevens, J., Rossor, M. N., Lees, A. J., & Fox, N. C. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.06.013 · Cited by 152 · see citing works
Dream phenomena induced by chronic Levodopa therapy
Sharf, B., Moskovitz, C., Lupton, M. D., & Klawans, H. L. (1978) · Journal of Neural Transmission · doi:10.1007/bf01579073 · Cited by 137 · see citing works
Stickgold, R., Malia, A., Fosse, R., Propper, R., & Hobson, J. A. (2001) · Sleep · doi:10.1093/sleep/24.2.171 · Cited by 136 · see citing works
Focal cortical and subcortical atrophy in early Parkinson's disease
Tinaz, S., Courtney, M. G., & Stern, C. E. (2010) · Movement Disorders · doi:10.1002/mds.23453 · Cited by 129 · see citing works
Thompson, D. F., & Pierce, D. R. (1999) · Annals of Pharmacotherapy · doi:10.1345/aph.18150 · Cited by 127 · see citing works
Methods correcting for multiple testing: operating characteristics
Brown, B. W., & Russell, K. E. (1997) · Statistics in Medicine · doi:10.1002/(sici)1097-0258(19971130)16:22 · Cited by 118 · see citing works
Correlation of Parkinson Disease Severity and18F-DTBZ Positron Emission Tomography
Hsiao, I., Weng, Y.-H., Hsieh, C., Lin, W., Wey, S., Kung, M., Yen, T., Lu, C., & Lin, K. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2014.290 · Cited by 118 · see citing works
The neural substrate for dreaming: is it a subsystem of the default network?
William Domhoff, G. (2011) · Consciousness and Cognition · doi:10.1016/j.concog.2011.03.001 · Cited by 118 · see citing works
Resting brain activity varies with dream recall frequency between subjects
Eichenlaub, J.-B., Nicolas, A., Daltrozzo, J., Redouté, J., Costes, N., & Ruby, P. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.6 · Cited by 107 · see citing works
Patton, M. H., Bizup, B. T., & Grace, A. A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2449-13.2013 · Cited by 94 · see citing works
Amygdala and hippocampus volumetry and diffusivity in relation to dreaming
De Gennaro, L., Cipolli, C., Cherubini, A., Assogna, F., Cacciari, C., Marzano, C., Curcio, G., Ferrara, M., Caltagirone, C., & Spalletta, G. (2011) · Human Brain Mapping · doi:10.1002/hbm.21120 · Cited by 79 · see citing works
Self-citationSleep and dreaming : origins, nature and functions
Cohen, D. B. (1979) · Cited by 78 · see citing works
White matter hyperintensities segmentation: a new semi-automated method
Iorio, M., Spalletta, G., Chiapponi, C., Luccichenti, G., Cacciari, C., Orfei, M. D., Caltagirone, C., & Piras, F. (2013) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2013.00076 · Cited by 65 · see citing works
Self-citationClinicopathological characteristics of freezing of gait in autopsy‐confirmed Parkinson's disease
Virmani, T., Moskowitz, C. B., Vonsattel, J., & Fahn, S. (2015) · Movement Disorders · doi:10.1002/mds.26346 · Cited by 56 · see citing works
De Gennaro, L., Marzano, C., Cipolli, C., & Ferrara, M. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.017 · Cited by 48 · see citing works
Self-citationAlexithymia and Dream Recall Upon Spontaneous Morning Awakening
Gennaro, L. D., Ferrara, M., Cristiani, R., Curcio, G., Martiradonna, V., & Bertini, M. (2003) · Psychosomatic Medicine · doi:10.1097/01.psy.0000058373.50240.71 · Cited by 46 · see citing works
Self-citationMcLaughlin, T., Blum, K., Oscar‐Berman, M., Febo, M., Agan, G., Fratantonio, J. L., Simpatico, T. A., & Gold, M. S. (2015) · Journal of Behavioral Addictions · doi:10.1556/2006.4.2015.008 · Cited by 44 · see citing works
Primary sleep disorder prevalence in patients with newly diagnosed Parkinson's disease
Prudon, B., Duncan, G. W., Khoo, T. K., Yarnall, A. J., Burn, D. J., & Anderson, K. N. (2013) · Movement Disorders · doi:10.1002/mds.25730 · Cited by 44 · see citing works
Recovery sleep after sleep deprivation almost completely abolishes dream recall
De Gennaro, L., Marzano, C., Moroni, F., Curcio, G., Ferrara, M., & Cipolli, C. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.09.030 · Cited by 44 · see citing works
Self-citationDream features in the early stages of Parkinson’s Disease
Bugalho, P., & Paiva, T. (2011) · Journal of Neural Transmission · doi:10.1007/s00702-011-0679-5 · Cited by 44 · see citing works
Manual MRI parcellation of the frontal lobe
Ranta, M. E., Crocetti, D., Clauss, J. A., Kraut, M. A., Mostofsky, S. H., & Kaufmann, W. E. (2009) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2009.01.006 · Cited by 39 · see citing works
Lack of polysomnographic Non‐REM sleep changes in early Parkinson's disease
Diederich, N. J., Rufra, O., Pieri, V., Hipp, G., & Vaillant, M. (2013) · Movement Disorders · doi:10.1002/mds.25520 · Cited by 32 · see citing works
Fagioli, I. (2002) · Sleep Medicine Reviews · doi:10.1053/smrv.2001.0214 · Cited by 31 · see citing works
Spoken and written dream communication: Differences and methodological aspects
Casagrande, M., & Cortini, P. (2008) · Consciousness and Cognition · doi:10.1016/j.concog.2007.11.002 · Cited by 26 · see citing works
Yang, H.-J., Kim, Y. E., Yun, J. Y., Kim, H., & Jeon, B. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091906 · Cited by 22 · see citing works
Rapid Eye Movement Sleep Behavior Disorder: A Window on the Emotional World of Parkinson Disease
Mariotti, P., Quaranta, D., Giacopo, R. D., Bentivoglio, A. R., Mazza, M., Martini, A., Canestri, J., & Marca, G. D. (2015) · SLEEP · doi:10.5665/sleep.4416 · Cited by 21 · see citing works
Pace-Schott, E. F. (2011) · Principles and Practice of Sleep Medicine · doi:10.1016/b978-1-4160-6645-3.00048-7 · Cited by 19 · see citing works
Modified leucotomy: report of 100 cases
Bradley, K. C., Dax, E. C., & Walsh, K. W. (1958) · Medical Journal of Australia · doi:10.5694/j.1326-5377.1958.tb86117.x · Cited by 13 · see citing works
D’Agostino, A., Gaspari, D. D., Antonini, A., Kantzas, I., Limosani, I., Manzone, M. L., Schiavella, M., Paganini, L., Siri, C., Rizzi, P., et al. (2010) · Journal of Neuropsychiatry · doi:10.1176/jnp.2010.22.4.395 · Cited by 8 · see citing works
High-resolution intersubject averaging and a coordinate system for the cortical surface
Fischl, B., Sereno, M. I., Tootell, R. B. H., & Dale, A. M. (1999) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1999)8:4
Flagged first, then by citations
Research works printed but not linked: 4
- American Psychiatric Association (2000): Diagnostic and Statistical Manual of Mental Disorders, 4th ed Washington, DC: Task Force. [Google Scholar]
- Pace‐Schott EF (2007): The frontal lobes and dreaming In: Barrett D, McNamara P, editors. The New Science of Dreaming. Westport, CT: Praeger, Greenwood Press; p 115–154. [Google Scholar]
- Pont‐Sunyer C, Hotter A, Gaig C, Seppi K, Compta Y, Katzenschlager R, Mas N, Hofeneder D, Brücke T, Bayés A, Wenzel K, Infante J, Zach H, Pirker W, Posada IJ, Alvarez R, Ispierto L, De Fàbregues O, Callén A, Palasi A, Aguilar M, Marti MJ, Valldeoriola F, Salamero M, Poewe W Tolosa E (2015): The Onset of Nonmotor Symptoms in Parkinson's disease (The ONSET PD Study). Mov Disord 30:229–237. [DOI] [PubMed] [Google Scholar]
- Sankoh AJ, Huque MF, Dubey SD (1997): Some comments on frequently used multiple endpoint adjustments methods in clinical trials. Stat Med 16:2529–2542. [DOI] [PubMed] [Google Scholar]
Cited by
Sorted by citations
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Siclari, F., Valli, K., & Arnulf, I. (2020) · The Lancet Neurology · doi:10.1016/s1474-4422(20)30275-1 · Cited by 98 · see citing works
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Cipolli, C., Ferrara, M., De Gennaro, L., & Plazzi, G. (2017) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2016.07.005 · Cited by 67 · see citing works
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Scarpelli, S., Bartolacci, C., D’Atri, A., Gorgoni, M., & De Gennaro, L. (2019) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph16193658 · Cited by 41 · see citing works
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Gott, J. A., Stücker, S., Kanske, P., Haaker, J., & Dresler, M. (2024) · Consciousness and Cognition · doi:10.1016/j.concog.2023.103608 · Cited by 25 · see citing works
- Authors
- De Gennaro, L., Lanteri, O., Piras, F., Scarpelli, S., Assogna, F., Ferrara, M., Caltagirone, C., & Spalletta, G.
- Affiliations
- Department of Psychology University of Rome “Sapienza,” Rome Italy
- Sapienza University of Rome (IT)
- Centro Ricerche Enrico Fermi (IT)
- Fondazione Santa Lucia (IT)
- Department of Life, Health and Environmental Sciences University of L'aquila Italy
- University of Rome Tor Vergata (IT)
- Baylor College of Medicine (US)
- Venue
- Human Brain Mapping
- Publisher
- Wiley
- Published
- 2015-12-24
- Volume
- 37
- Issue
- 3
- Pages
- 1136-1147
- ISSN
- 1065-9471 (ISSN-L)
- 1097-0193
- PMC
- PMC6867535
- OpenAlex
- W2198267268
- Cited by
- 45
- References
- 70
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 1 · 2023: 2 · 2022: 7 · 2021: 4 · 2020: 7 · 2019: 6 · 2018: 4 · 2017: 3 · 2016: 3
- FWCI
- 2.01
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Human Brain Mapping (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
- Archivio Istituzionale della Ricerca - Università degli Studi dell Aquila (submittedVersion)
- Funders
- Luigi De Gennaro from Ministero della Salute (Ministry of Health) (RF-2009-1528677)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- dream recall, dopaminergic system, Parkinson's disease, dopamine agonists, medial prefrontal cortex, amygdala, hippocampus, dream vividness, dream bizarreness, mesolimbic system, subcortical volume, cortical thickness
- MeSH terms
- Adult, Aged, Antiparkinson Agents, Brain, Dreams, Emotions, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Organ Size, Parkinson Disease, Mental Recall, Sleep, Dopamine Agonists
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