G. Clément, Fundamentals of Space Medicine, 2011.
DOI : 10.1007/978-1-4419-9905-4

J. R. Lackner and P. Dizio, Space motion sickness, Experimental Brain Research, vol.13, issue.4???6, pp.377-399, 2006.
DOI : 10.1007/978-1-4757-5702-6

G. R. Holstein, E. Kukielka, and G. P. Martinelli, Anatomical observations of the rat cerebellar nodulus after 24 hr of spaceflight, J. Gravit. Physiol, vol.6, pp.47-50, 1999.

A. B. Newberg, Changes in the central nervous system and their clinical correlates during long-term spaceflight, Aviat. Space. Environ. Med, vol.65, pp.562-572, 1994.

M. D. Ross, A Spaceflight Study of Synaptic Plasticity in Adult Rat Vestibular Maculas, Acta Oto-Laryngologica, vol.13, issue.sup516, pp.1-14, 1994.
DOI : 10.1002/cne.902090407

A. Van-ombergen, Spaceflight-induced neuroplasticity in humans as measured by MRI: what do we know so far?, npj Microgravity, vol.86, issue.1, 2017.
DOI : 10.1007/978-3-7091-6792-2

A. Demertzi, Cortical reorganization in an astronaut?s brain after long-duration spaceflight, Brain Structure and Function, vol.23, issue.1, pp.2873-2876, 2016.
DOI : 10.1111/j.1749-6632.1992.tb25253.x
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884200

N. M. Navasiolava, Long-term dry immersion: review and prospects, European Journal of Applied Physiology, vol.180, issue.1 Suppl, pp.1235-1260, 2011.
DOI : 10.1503/cmaj.090628

A. Pavy-le-traon, M. Heer, M. V. Narici, J. Rittweger, and J. Vernikos, From space to Earth: Advances in human physiology from 20 years of bed rest studies, European Journal of Applied Physiology, vol.101, 1986.

F. Karmali and M. Shelhamer, The dynamics of parabolic flight: Flight characteristics and passenger percepts, Acta Astronautica, vol.63, issue.5-6, pp.594-602, 2008.
DOI : 10.1016/j.actaastro.2008.04.009

B. Lv, Q. Shao, Z. Chen, L. Ma, and T. Wu, Effects of acute electromagnetic fields exposure on the interhemispheric homotopic functional connectivity during resting state, Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBS, pp.2015-1813, 2015.

E. Hermans, M. Henckens, M. Jöels, and G. Fernandez, Dynamic adaptation of large-scale brain networks in response to acute stressors, Trends in Neurosciences, vol.37, issue.6, pp.304-314, 2014.
DOI : 10.1016/j.tins.2014.03.006

H. Van-marle, E. Hermans, S. Qin, and G. Fernandez, Enhanced resting-state connectivity of amygdala in the immediate aftermath of acute psychological stress, NeuroImage, vol.53, issue.1, pp.348-354, 2010.
DOI : 10.1016/j.neuroimage.2010.05.070

E. Tagliazucchi, Increased Global Functional Connectivity Correlates with LSD-Induced Ego Dissolution, Current Biology, vol.26, issue.8, pp.1043-1050, 2016.
DOI : 10.1016/j.cub.2016.02.010
URL : https://www.repository.cam.ac.uk/bitstream/1810/253667/1/Tagliazucchi%20et%20al%202016%20Current%20Biology.pdf

R. L. Carhart-harris, Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin, Proc. Natl. Acad. Sci. USA, pp.2138-2181, 2012.
DOI : 10.1016/j.neuroimage.2003.11.025

C. Lopez, C. Bachofner, M. Mercier, and O. Blanke, Gravity and observer's body orientation influence the visual perception of human body postures, Journal of Vision, vol.9, issue.5, pp.1-14, 2009.
DOI : 10.1167/9.5.1

J. R. Lackner and P. Dizio, Multisensory, cognitive, and motor influences on human spatial orientation in weightlessness, J Vestib Res, vol.3, pp.361-372, 1993.

A. Van-ombergen, The effect of spaceflight and microgravity on the human brain, Journal of Neurology, vol.141, issue.12, 2017.
DOI : 10.1038/s41526-016-0010-8

A. B. Newberg and A. Alavi, Changes in the central nervous system during long-duration space flight: Implications for neuro-imaging, Advances in Space Research, vol.22, issue.2, pp.185-196, 1998.
DOI : 10.1016/S0273-1177(98)80010-0

B. B. Biswal, J. Van-kylen, and J. S. Hyde, Simultaneous assessment of flow and BOLD signals in resting-state functional connectivity maps, NMR in Biomedicine, vol.17, issue.4-5, pp.165-170, 1997.
DOI : 10.1161/01.STR.5.2.219

M. Lochner and A. J. Thompson, The muscarinic antagonists scopolamine and atropine are competitive antagonists at 5-HT3 receptors, Neuropharmacology, vol.108, pp.220-228, 2016.
DOI : 10.1016/j.neuropharm.2016.04.027
URL : http://doi.org/10.1016/j.neuropharm.2016.04.027

C. D. Wood, J. E. Manno, B. R. Manno, R. C. Odenheimer, and L. Bairnsfather, The effect of antimotion sickness drugs on habituation to motion, Aviat. Sp. Environ. Med, vol.57, pp.539-542, 1986.

A. Van-ombergen, B. D. Lawson, and F. L. Wuyts, Motion sickness and sopite syndrome associated with parabolic flights: a case report, International Journal of Audiology, vol.55, issue.3, pp.189-94, 2016.
DOI : 10.1152/japplphysiol.00149.2015

M. W. Johns, A New Method for Measuring Daytime Sleepiness: The Epworth Sleepiness Scale, Sleep, vol.14, issue.6, pp.540-545, 1991.
DOI : 10.1093/sleep/14.6.540

D. Watson, L. A. Clark, and A. Tellegen, Development and validation of brief measures of positive and negative affect: The PANAS scales., Journal of Personality and Social Psychology, vol.54, issue.6, pp.1063-1070, 1988.
DOI : 10.1037/0022-3514.54.6.1063

P. Gianaros and E. Muth, A questionnaire for the assessment of the multiple dimensions of motion sickness, Aviat. Sp. Environ. Med, vol.72, pp.115-119, 2001.

J. E. Bos, S. N. Mackinnon, and A. Patterson, Motion sickness symptoms in a ship motion simulator: Effects of inside, outside, and no view, Aviat. Sp. Environ. Med, vol.76, pp.1111-1118, 2005.

Y. Behzadi, K. Restom, J. Liau, and T. Liu, A component based noise correction method (CompCor) for BOLD and perfusion based fMRI, NeuroImage, vol.37, issue.1, pp.90-101, 2007.
DOI : 10.1016/j.neuroimage.2007.04.042
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2214855

X. J. Chai, A. N. Castañán, D. Öngür, and S. Whitfield-gabrieli, Anticorrelations in resting state networks without global signal regression, NeuroImage, vol.59, issue.2, pp.1420-1428, 2012.
DOI : 10.1016/j.neuroimage.2011.08.048
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3230748

M. Raichle, The Restless Brain, Brain Connectivity, vol.1, issue.1, pp.3-12, 2011.
DOI : 10.1089/brain.2011.0019
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621343

R. Martuzzi, A whole-brain voxel based measure of intrinsic connectivity contrast reveals local changes in tissue connectivity with anesthetic without a priori assumptions on thresholds or regions of interest, NeuroImage, vol.58, issue.4, pp.1044-1050, 2011.
DOI : 10.1016/j.neuroimage.2011.06.075

D. Vatansever, A. E. Manktelow, B. J. Sahakian, D. K. Menon, and E. A. Stamatakis, Angular default mode network connectivity across working memory load. Hum, Brain Mapp, pp.10-1002, 2016.
DOI : 10.1002/hbm.23341

E. Pravatà, Hyperconnectivity of the dorsolateral prefrontal cortex following mental effort in multiple sclerosis patients with cognitive fatigue, Multiple Sclerosis Journal, vol.22, issue.13, pp.10-1177, 2016.
DOI : 10.1073/pnas.1110024108

A. M. Muller, S. Mérillat, and L. Jäncke, Older but still fluent? Insights from the intrinsically active baseline configuration of the aging brain using a data driven graph-theoretical approach, NeuroImage, vol.127, pp.346-362, 2016.
DOI : 10.1016/j.neuroimage.2015.12.027

E. A. Layden, Perceived social isolation is associated with altered functional connectivity in neural networks associated with tonic alertness and executive control, NeuroImage, vol.145, p.50, 2016.
DOI : 10.1016/j.neuroimage.2016.09.050

J. M. Goldberg, The Vestibular System: A Sixth Sense. The Vestibular System: A Sixth Sense, 2012.
DOI : 10.1093/acprof:oso/9780195167085.001.0001

A. Kheradmand, A. Lasker, and D. S. Zee, Transcranial Magnetic Stimulation (TMS) of the Supramarginal Gyrus: A Window to Perception of Upright, Cerebral Cortex, vol.25, issue.3, pp.765-771, 2015.
DOI : 10.1093/cercor/bht267

F. Fiori, M. Candidi, A. Acciarino, N. David, and S. M. Aglioti, The right temporo parietal junction plays a causal role in maintaining the internal representation of verticality, J. Neurophysiol, vol.3, p.2892015, 2015.

H. Block, A. Bastian, and P. Celnik, Virtual Lesion of Angular Gyrus Disrupts the Relationship between Visuoproprioceptive Weighting and Realignment, Journal of Cognitive Neuroscience, vol.4, issue.4, pp.636-684, 2013.
DOI : 10.3758/BF03198798

G. Bosco, M. Carrozzo, and F. Lacquaniti, Contributions of the Human Temporoparietal Junction and MT/V5+ to the Timing of Interception Revealed by Transcranial Magnetic Stimulation, Journal of Neuroscience, vol.28, issue.46, pp.12071-12084, 2008.
DOI : 10.1523/JNEUROSCI.2869-08.2008

P. Senot, M. Zago, F. Lacquaniti, and J. Mcintyre, Anticipating the Effects of Gravity When Intercepting Moving Objects: Differentiating Up and Down Based on Nonvisual Cues, Journal of Neurophysiology, vol.94, issue.6, pp.4471-4480, 2005.
DOI : 10.1152/jn.00527.2005

P. Senot, When Up Is Down in 0g: How Gravity Sensing Affects the Timing of Interceptive Actions, Journal of Neuroscience, vol.32, issue.6, pp.1969-1973, 2012.
DOI : 10.1523/JNEUROSCI.3886-11.2012

I. Indovina, Representation of Visual Gravitational Motion in the Human Vestibular Cortex, Science, vol.308, issue.5720, pp.416-425, 2005.
DOI : 10.1126/science.1107961

H. J. Block and A. J. Bastian, Sensory weighting and realignment: independent compensatory processes, Journal of Neurophysiology, vol.106, issue.1, pp.59-70, 2011.
DOI : 10.1152/jn.00641.2010
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129718

R. Roll, Proprioceptive information processing in weightlessness, Experimental Brain Research, vol.122, issue.4, pp.393-402, 1998.
DOI : 10.1007/s002210050527

B. Baier, J. Suchan, H. O. Karnath, and M. Dieterich, Neural correlates of disturbed perception of verticality, Neurology, vol.78, issue.10, pp.728-735, 2012.
DOI : 10.1212/WNL.0b013e318248e544

J. Barra, Humans use internal models to construct and update a sense of verticality, Brain, vol.133, issue.12, pp.3552-3563, 2010.
DOI : 10.1093/brain/awq311
URL : https://hal.archives-ouvertes.fr/hal-00775946

S. Ionta, Multisensory Mechanisms in Temporo-Parietal Cortex Support Self-Location and First-Person Perspective, Neuron, vol.70, issue.2, pp.363-374, 2011.
DOI : 10.1016/j.neuron.2011.03.009
URL : http://doi.org/10.1016/j.neuron.2011.03.009

C. Pfeiffer, A. Serino, and O. Blanke, The vestibular system: a spatial reference for bodily self-consciousness, Frontiers in Integrative Neuroscience, vol.60, p.31, 2014.
DOI : 10.1016/j.neuroimage.2011.12.032

C. Lopez, O. Blanke, and F. Mast, The vestibular cortex in the human brain revealed by coordinate-based activation likelihood estimation meta-analysis, Neuroscience, vol.60, pp.162-169, 2012.

Z. Eulenburg, P. Caspers, S. Roski, C. Eickhoff, and S. B. , Meta-analytical definition and functional connectivity of the human vestibular cortex, NeuroImage, vol.60, issue.1, pp.162-169, 2012.
DOI : 10.1016/j.neuroimage.2011.12.032

W. O. Guldin and O. J. Grüsser, Is there a vestibular cortex?, Trends in Neurosciences, vol.21, issue.6, pp.254-259, 1998.
DOI : 10.1016/S0166-2236(97)01211-3

S. Eickhoff, K. Amunts, H. Mohlberg, and K. Zilles, The Human Parietal Operculum. II. Stereotaxic Maps and Correlation with Functional Imaging Results, Cerebral Cortex, vol.16, issue.2, pp.268-279, 2006.
DOI : 10.1093/cercor/bhi106
URL : http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.563.1947

O. Blanke, Multisensory brain mechanisms of bodily self-consciousness, Nature Reviews Neuroscience, vol.40, pp.556-71, 2012.
DOI : 10.1016/S0168-0102(01)00225-5

S. Gallagher, Philosophical conceptions of the self: implications for cognitive science, Trends in Cognitive Sciences, vol.4, issue.1, pp.14-21, 2000.
DOI : 10.1016/S1364-6613(99)01417-5

J. Isnard, M. Guénot, M. Sindou, and F. Mauguière, Clinical Manifestations of Insular Lobe Seizures: A Stereo-electroencephalographic Study, Epilepsia, vol.66, issue.9, pp.1079-1090, 2004.
DOI : 10.1002/ana.10726

D. K. Nguyen, Revisiting the role of the insula in refractory partial epilepsy, Epilepsia, vol.5, issue.Suppl 2, pp.510-520, 2009.
DOI : 10.1111/j.1528-1167.2008.01758.x

L. Heydrich, C. Lopez, M. Seeck, and O. Blanke, Partial and full own-body illusions of epileptic origin in a child with right temporoparietal epilepsy, Epilepsy & Behavior, vol.20, issue.3, pp.583-586, 2011.
DOI : 10.1016/j.yebeh.2011.01.008

O. Blanke, S. Ortigue, T. Landis, and M. Seeck, Neuropsychology: Stimulating illusory own-body perceptions, Nature, vol.80, issue.6904, pp.269-270, 2002.
DOI : 10.1016/S0010-9452(13)80115-3

D. De-ridder, K. Van-laere, P. Dupont, T. Menovsky, and P. Van-de-heyning, Visualizing Out-of-Body Experience in the Brain, New England Journal of Medicine, vol.357, issue.18, pp.1829-1833, 2007.
DOI : 10.1056/NEJMoa070010

A. Graybiel and R. Kellogg, The inversion illusion in parabolic flight: its probable dependence on otolith function, Aerosp. Med, vol.38, pp.1099-1103, 1967.

D. A. Pérennou, Lateropulsion, pushing and verticality perception in hemisphere stroke: a causal relationship?, Brain, vol.131, issue.9, pp.2401-2413, 2008.
DOI : 10.1093/brain/awn170

M. Dieterich, Dominance for Vestibular Cortical Function in the Non-dominant Hemisphere, Cerebral Cortex, vol.13, issue.9, pp.994-1007, 2003.
DOI : 10.1093/cercor/13.9.994

S. Bense, Metabolic changes in vestibular and visual cortices in acute vestibular neuritis, Annals of Neurology, vol.5, issue.5, pp.624-630, 2004.
DOI : 10.1212/WNL.51.3.838

H. Lee, Anatomical Traces of Vocabulary Acquisition in the Adolescent Brain, Journal of Neuroscience, vol.27, issue.5, pp.1184-1193, 2007.
DOI : 10.1523/JNEUROSCI.4442-06.2007

G. Bottini, Identification of the central vestibular projections in man: a positron emission tomography activation study, Experimental Brain Research, vol.99, issue.1, pp.164-169, 1994.
DOI : 10.1007/BF00241421

E. Vitte, Activation of the hippocampal formation by vestibular stimulation: a functional magnetic resonance imaging study, Experimental Brain Research, vol.112, issue.3, pp.523-529, 1996.
DOI : 10.1007/BF00227958

M. Suzuki, Cortical and subcortical vestibular response to caloric stimulation detected by functional magnetic resonance imaging, Cognitive Brain Research, vol.12, issue.3, pp.441-449, 2001.
DOI : 10.1016/S0926-6410(01)00080-5

A. Deutschländer, Sensory system interactions during simultaneous vestibular and visual stimulation in PET, Human Brain Mapping, vol.11, issue.Suppl, pp.92-103, 2002.
DOI : 10.1006/nimg.1995.1023

S. Bense, T. Stephan, T. Yousry, T. Brandt, and M. Dieterich, Multisensory cortical signal increases and decreases during vestibular galvanic stimulation (fMRI), J. Neurophysiol, vol.85, pp.886-899, 2001.

T. Stephan, Functional MRI of galvanic vestibular stimulation with alternating currents at different frequencies, NeuroImage, vol.26, issue.3, pp.721-732, 2005.
DOI : 10.1016/j.neuroimage.2005.02.049

L. Q. Uddin, Dissociable Connectivity within Human Angular Gyrus and Intraparietal Sulcus: Evidence from Functional and Structural Connectivity, Cerebral Cortex, vol.20, issue.11, pp.2636-2646, 2010.
DOI : 10.1093/cercor/bhq011
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951845

M. D. Fox, The human brain is intrinsically organized into dynamic, 2005.
DOI : 10.1073/pnas.0504136102
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1157105

P. Fransson, Spontaneous low-frequency BOLD signal fluctuations: An fMRI investigation of the resting-state default mode of brain function hypothesis, Human Brain Mapping, vol.8, issue.1, pp.15-29, 2005.
DOI : 10.1038/nrn894

S. Whitfield-gabrieli, Hyperactivity and hyperconnectivity of the default network in schizophrenia and in first-degree relatives of persons with schizophrenia, Proc. Natl. Acad. Sci. USA, pp.1279-84, 2009.
DOI : 10.1002/(SICI)1097-0193(1997)5:2<133::AID-HBM7>3.0.CO;2-4

A. Vanhaudenhuyse, Two Distinct Neuronal Networks Mediate the Awareness of Environment and of Self, Journal of Cognitive Neuroscience, vol.174, issue.3, pp.570-578, 2011.
DOI : 10.1093/brain/124.7.1263

A. Demertzi, A. Soddu, M. Faymonville, M. A. Bahri, and O. Gosseries, Hypnotic modulation of resting state fMRI default mode and extrinsic network connectivity. Slow Brain Oscillations of Sleep Resting State and Vigilance 193, 2011.
DOI : 10.1016/b978-0-444-53839-0.00020-x
URL : http://orbi.ulg.ac.be/bitstream/2268/99391/1/demertzi_hypnosis_PBR2011.pdf

J. B. Keller, Resting-state anticorrelations between medial and lateral prefrontal cortex: Association with working memory, aging, and individual differences, Cortex, vol.64, pp.271-280, 2015.
DOI : 10.1016/j.cortex.2014.12.001
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346444

D. Perri and C. , Neural correlates of consciousness in patients who have emerged from a minimally conscious state: a cross-sectional multimodal imaging study, The Lancet Neurology, vol.15, issue.8, pp.830-872, 2016.
DOI : 10.1016/S1474-4422(16)00111-3

A. Demertzi, A. Soddu, and S. Laureys, Consciousness supporting networks, Consciousness supporting networks, pp.239-244, 2013.
DOI : 10.1016/j.conb.2012.12.003
URL : http://orbi.ulg.ac.be/bitstream/2268/152565/1/Demertzi_CurOpNeurob_2013.pdf

A. Demertzi, Looking for the Self in Pathological Unconsciousness, Frontiers in Human Neuroscience, vol.7, pp.1-6, 2013.
DOI : 10.3389/fnhum.2013.00538

J. E. Bos and W. Bles, Modelling motion sickness and subjective vertical mismatch detailed for vertical motions, Brain Research Bulletin, vol.47, issue.5, pp.537-542, 1998.
DOI : 10.1016/S0361-9230(98)00088-4

P. Denise, C. Darlot, J. Droulez, B. Cohen, and A. Berthoz, Motion perceptions induced by off-vertical axis rotation (OVAR) at small angles of tilt, Experimental Brain Research, vol.47, issue.1, pp.106-114, 1988.
DOI : 10.1007/BF00279665

J. Neimer, S. Eskiizmirliler, J. Dominey-ventre, and C. Darlot, Trains with a view to sickness, Current Biology, vol.11, issue.14, pp.549-550, 2001.
DOI : 10.1016/S0960-9822(01)00339-6
URL : https://hal.archives-ouvertes.fr/hal-00332315

U. Ebert, M. Siepmann, R. Oertel, K. A. Wesnes, and W. Kirch, Pharmacokinetics and Pharmacodynamics of Scopolamine after Subcutaneous Administration, The Journal of Clinical Pharmacology, vol.55, issue.8, pp.720-726, 1998.
DOI : 10.1016/0013-4694(83)90124-4

R. Sperling, Functional MRI detection of pharmacologically induced memory impairment, Proceedings of the National Academy of Sciences, vol.290, issue.5500, pp.455-460, 2002.
DOI : 10.1126/science.290.5500.2315

K. Schon, Scopolamine Reduces Persistent Activity Related to Long-Term Encoding in the Parahippocampal Gyrus during Delayed Matching in Humans, Journal of Neuroscience, vol.25, issue.40, pp.9112-9135, 2005.
DOI : 10.1523/JNEUROSCI.1982-05.2005

B. Voss, Cholinergic blockade under working memory demands encountered by increased rehearsal strategies: evidence from fMRI in healthy subjects, European Archives of Psychiatry and Clinical Neuroscience, vol.260, issue.Suppl 2, pp.329-339, 2012.
DOI : 10.1007/s00406-010-0160-8

D. Shah, Acute modulation of the cholinergic system in the mouse brain detected by pharmacological resting-state functional MRI, NeuroImage, vol.109, pp.151-159, 2015.
DOI : 10.1016/j.neuroimage.2015.01.009

J. Lackner, Motion sickness: more than nausea and vomiting, Experimental Brain Research, vol.101, issue.Pt 2, pp.2493-2510, 2014.
DOI : 10.1046/j.1440-1681.2002.03612.x
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112051

M. Alda, Validation of the Spanish version of the Multidimensional State Boredom Scale (MSBS), Health and Quality of Life Outcomes, vol.90, issue.1, p.59, 2015.
DOI : 10.1037/0022-3514.90.2.288

S. Schneider, Parabolic flight experience is related to increased release of stress hormones, European Journal of Applied Physiology, vol.94, issue.Suppl 9, pp.301-308, 2007.
DOI : 10.1080/00222895.1978.10735150

S. Schneider, The effect of parabolic flight on perceived physical, motivational and psychological state in men and women: Correlation with neuroendocrine stress parameters and electrocortical activity, Stress, vol.26, issue.4, pp.336-349, 2009.
DOI : 10.1016/S0306-4530(01)00025-7

C. Strewe, for their assistance and expertise in the preparation of the parabolic flight campaigns. Also, we would like to thank Dr) and Federico Raimondo, MSc (Department of Computer Science, University of Buenos Aires, Argentina) for methods consultation and code sharing, Enzo Tagliazucchi (Institut du Cerveau et de la Moelle Epinière ? ICM This work was supported by the European Space Agency (ESA) and BELSPO Prodex the Research Foundation Flanders (FWO Vlaanderen) the Belgian National Funds for Scientific Research (FRS-FNRS), the Wallonie-Bruxelles International, the James McDonnell Foundation, IAP research network P7/06 of the Belgian Government (Belgian Science Policy), the European Commission, the Public Utility Foundation 'Université Européenne du Travail' , " Fondazione Europea di Ricerca Biomedica " , the Bial Foundation, the Human Brain Project, pp.673-680, 2012.

H. The and L. , A.V.O. is a Research Fellow of the Research Foundation Flanders (Belgium, FWO Vlaanderen), B.J. is Postdoctoral Fellow at FWO Vlaanderen, A.D. is Postdoctoral Fellow at FRS-FNRS, S.L. is Research Director at FRS-FNRS
URL : https://hal.archives-ouvertes.fr/jpa-00245245