Uncertainty-based competition between prefrontal and dorsolateral striatal systems for behavioral control, Nature Neuroscience, vol.58, issue.12, pp.1704-1711, 2005. ,
DOI : 10.1038/nn1560
Habits, Rituals, and the Evaluative Brain, Annual Review of Neuroscience, vol.31, issue.1, pp.359-387, 2008. ,
DOI : 10.1146/annurev.neuro.29.051605.112851
Different time courses of learning-related activity in the prefrontal cortex and striatum, Nature, vol.16, issue.7028, pp.873-876, 2005. ,
DOI : 10.1126/science.274.5286.427
Multiple Representations of Belief States and Action Values in Corticobasal Ganglia Loops, Annals of the New York Academy of Sciences, vol.20, issue.1, pp.213-228, 2007. ,
DOI : 10.1038/nrn1884
Surgical treatment of dyskinesia in Parkinson's disease, Front Neurol, vol.5, p.65, 2014. ,
Pallidal surgery for the treatment of primary generalized dystonia: Long-term follow-up, Clinical Neurology and Neurosurgery, vol.110, issue.2, pp.145-150, 2008. ,
DOI : 10.1016/j.clineuro.2007.10.003
Globus pallidus deep brain stimulation for generalized dystonia: Clinical and PET investigation, Neurology, vol.53, issue.4, pp.871-874, 1999. ,
DOI : 10.1212/WNL.53.4.871
Treatment of Wilson's disease motor complications with deep brain stimulation, Annals of the New York Academy of Sciences, vol.19, issue.Suppl. 1, pp.16-23, 2014. ,
DOI : 10.1111/nyas.12372
Deep brain stimulation for hyperkinetics disorders: dystonia, tardive dyskinesia, and tics, Current Opinion in Neurology, vol.23, pp.420-425, 2010. ,
DOI : 10.1097/WCO.0b013e32833b7798
Motor Sequences and the Basal Ganglia: Kinematics, Not Habits, Journal of Neuroscience, vol.30, issue.22, pp.7685-7690, 2010. ,
DOI : 10.1523/JNEUROSCI.0163-10.2010
Influence of globus pallidus on arm movements in monkeys. I. Effects of kainic acid-induced lesions, J Neurophysiol, vol.52, pp.290-304, 1984. ,
Arm movement performance during reversible basal ganglia lesions in the monkey, Experimental Brain Research, vol.39, issue.2, pp.217-228, 1980. ,
DOI : 10.1007/BF00237552
Basal ganglia motor control. III. Pallidal ablation: normal reaction time, muscle cocontraction, and slow movement, J Neurophysiol, vol.65, pp.330-351, 1991. ,
Some parameters of behavioral contrast and allocation of interim behavior in rats, Journal of the Experimental Analysis of Behavior, vol.44, issue.3, pp.325-335, 1985. ,
DOI : 10.1901/jeab.1985.44-325
Coyotes (Canis latrans) and the matching law, Behavioural Processes, vol.82, issue.2, pp.178-183, 2009. ,
DOI : 10.1016/j.beproc.2009.06.005
The matching law in and within groups of rats1, Journal of the Experimental Analysis of Behavior, vol.27, issue.1, pp.183-194, 1977. ,
DOI : 10.1901/jeab.1977.27-183
Formal properties of the matching law1, Journal of the Experimental Analysis of Behavior, vol.21, issue.1, pp.159-164, 1974. ,
DOI : 10.1901/jeab.1974.21-159
Expectation of reward modulates cognitive signals in the basal ganglia, Nat Neurosci, vol.1, pp.411-416, 1998. ,
Complex Population Response of Dorsal Putamen Neurons Predicts the Ability to Learn, PLoS ONE, vol.191, issue.11, p.80683, 2013. ,
DOI : 10.1371/journal.pone.0080683.s001
URL : https://hal.archives-ouvertes.fr/hal-01160401
Value Representations in the Primate Striatum during??Matching Behavior, Neuron, vol.58, issue.3, pp.451-463, 2008. ,
DOI : 10.1016/j.neuron.2008.02.021
Concurrent schedule assessment of food preference in cows, Journal of the Experimental Analysis of Behavior, vol.32, issue.2, pp.245-254, 1979. ,
DOI : 10.1901/jeab.1979.32-245
Midbrain dopamine neurons encode decisions for future action, Nature Neuroscience, vol.92, issue.8, pp.1057-1063, 2006. ,
DOI : 10.1038/nn1743
Brain Hemispheres Selectively Track the Expected Value of Contralateral Options, Journal of Neuroscience, vol.29, issue.43, pp.13465-13472, 2009. ,
DOI : 10.1523/JNEUROSCI.1500-09.2009
Why am I lost without dopamine? Effects of 6-OHDA lesion on the encoding of reward and decision process in CA3, Neurobiology of Disease, vol.59, pp.151-164, 2013. ,
DOI : 10.1016/j.nbd.2013.07.014
URL : https://hal.archives-ouvertes.fr/hal-01160385
Representation of Action-Specific Reward Values in the Striatum, Science, vol.310, issue.5752, pp.1337-1340, 2005. ,
DOI : 10.1126/science.1115270
Shaping of Motor Responses by Incentive Values through the Basal Ganglia, Journal of Neuroscience, vol.27, issue.5, pp.1176-1183, 2007. ,
DOI : 10.1523/JNEUROSCI.3745-06.2007
The rhesus monkey brain in stereotaxic coordinates, 2000. ,
Competition between Feedback Loops Underlies Normal and Pathological Dynamics in the Basal Ganglia, Journal of Neuroscience, vol.26, issue.13, pp.3567-3583, 2006. ,
DOI : 10.1523/JNEUROSCI.5050-05.2006
URL : https://hal.archives-ouvertes.fr/hal-00094738
Interaction between cognitive and motor cortico-basal ganglia loops during decision making: a computational study, Journal of Neurophysiology, vol.109, issue.12, pp.3025-3040, 2013. ,
DOI : 10.1152/jn.00026.2013
URL : https://hal.archives-ouvertes.fr/hal-00828004
A long journey into reproducible computational neuroscience, Frontiers in Computational Neuroscience, vol.515, p.30, 2015. ,
DOI : 10.1038/515151a
URL : https://hal.archives-ouvertes.fr/hal-01109483
The functional anatomy of basal ganglia disorders, Trends in Neurosciences, vol.12, issue.10, pp.366-375, 1989. ,
DOI : 10.1016/0166-2236(89)90074-X
Preparation for movement: neural representations of intended direction in three motor areas of the monkey, J Neurophysiol, vol.64, pp.133-150, 1990. ,
Functional Organization of the Basal Ganglia: Contributions of Single-Cell Recording Studies, Ciba Found Sym, vol.2, pp.64-82, 1984. ,
DOI : 10.1002/9780470720882.ch5
Pallidal discharge related to the kinematics of reaching movements in two dimensions, J Neurophysiol, vol.77, pp.1051-1074, 1997. ,
MOTOR FUNCTION OF THE MONKEY GLOBUS PALLIDUS, Brain, vol.114, issue.4, pp.1685-1702, 1991. ,
DOI : 10.1093/brain/114.4.1685
Reinforcement Learning in Continuous Time and Space, Neural Computation, vol.3, issue.1, pp.219-245, 2000. ,
DOI : 10.1109/9.580874
Separate neural substrates for skill learning and performance in the ventral and dorsal striatum, Nature Neuroscience, vol.113, issue.1, pp.126-131, 2007. ,
DOI : 10.1016/S0306-4522(99)00575-8
Hold Your Horses: Impulsivity, Deep Brain Stimulation, and Medication in Parkinsonism, Science, vol.318, issue.5854, pp.1309-1312, 2007. ,
DOI : 10.1126/science.1146157
Parkinson's Disease, the Subthalamic Nucleus, Inhibition, and Impulsivity, Movement Disorders, vol.3, issue.4 Suppl 1, pp.128-140, 2015. ,
DOI : 10.1002/mds.26049
Bilateral Lesions of the Subthalamic Nucleus Induce Multiple Deficits in an Attentional Task in Rats, European Journal of Neuroscience, vol.32, issue.suppl., pp.2086-2099, 1997. ,
DOI : 10.1111/j.1460-9568.1997.tb01376.x
Basal ganglia preferentially encode context dependent choice in a twoarmed bandit task, Front Syst Neurosci, vol.5, p.23, 2011. ,
URL : https://hal.archives-ouvertes.fr/hal-01155573
Analysis of Probabilistic Classification Learning in Patients With Parkinson's Disease Before and After Pallidotomy Surgery, Learning & Memory, vol.10, issue.3, pp.226-236, 2003. ,
DOI : 10.1101/lm.45903
What can man do without basal ganglia motor output? The effect of combined unilateral subthalamotomy and pallidotomy in a patient with Parkinson's disease, Experimental Neurology, vol.220, issue.2, pp.283-292, 2009. ,
DOI : 10.1016/j.expneurol.2009.08.030