Microcircuitry of the direct and indirect pathways of the basal ganglia.

[1]  J. M. Kemp.  The termination of strio-pallidal and strio-nigral fibres. , 1970, Brain research.

[2]  T. Powell,et al.  The termination of fibres from the cerebral cortex and thalamus upon dendritic spines in the caudate nucleus: a study with the Golgi method. , 1971, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[3]  T. Powell,et al.  The structure of the caudate nucleus of the cat: light and electron microscopy. , 1971, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[4]  H. Künzle.  Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study inMacaca fascicularis , 1975, Brain Research.

[5]  M. Sugimori,et al.  Monosynaptic inputs to caudate neurons identified by intracellular injection of horseradish peroxidase , 1976, Brain Research.

[6]  W. Nauta,et al.  An intricately patterned prefronto‐caudate projection in the rhesus monkey , 1977, The Journal of comparative neurology.

[7]  H. Nauta.  Projections of the pallidal complex: An autoradiographic study in the cat , 1979, Neuroscience.

[8]  P. Somogyi,et al.  An approach to tracing neuron networks in the cerebral cortex and basal ganglia. Combination of golgi staining, retrograde transport of horseradish peroxidase and anterograde degeneration of synaptic boutons in the same material , 1979, Neuroscience.

[9]  J. E. Vaughn,et al.  The GABA Neurons and their axon terminals in rat corpus striatum as demonstrated by GAD immunocytochemistry , 1979, The Journal of comparative neurology.

[10]  K. Usunoff,et al.  Corticosubthalamic projection in the cat: an electron microscopic study , 1979, Brain Research.

[11]  Charles J. Wilson,et al.  Fine structure and synaptic connections of the common spiny neuron of the rat neostriatum: A study employing intracellular injection of horseradish peroxidase , 1980 .

[12]  T. Hattori,et al.  Single subthalamic nucleus neurons project to both the globus pallidus and substantia nigra in rat , 1980, The Journal of comparative neurology.

[13]  C. Sotelo,et al.  Dopaminergic dendrites in the pars reticulata of the rat substantia nigra and their striatal input. combined immunocytochemical localization of tyrosine hydroxylase and anterograde degeneration , 1981, Neuroscience.

[14]  P. Somogyi,et al.  Monosynaptic input from the nucleus accumbens-ventral striatum region to retrogradely labelled nigrostriatal neurones , 1981, Brain Research.

[15]  P Pasik,et al.  A Golgi and ultrastructural study of the monkey globus pallidus , 1982, The Journal of comparative neurology.

[16]  P. Groves.  A theory of the functional organization of the neostriatum and the neostriatal control of voluntary movement , 1983, Brain Research Reviews.

[17]  André Parent,et al.  The pallidointralaminar and pallidonigral projections in primate as studied by retrograde double-labeling method , 1983, Brain Research.

[18]  A. Jayaraman.  Topographic organization and morphology of peripallidal and pallidal cells projecting to the striatum in cats , 1983, Brain Research.

[19]  M. D. Crutcher,et al.  Relations between movement and single cell discharge in the substantia nigra of the behaving monkey , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[20]  C. Hammond,et al.  Intracellular labelling of rat subthalamic neurones with horseradish peroxidase: Computer analysis of dendrites and characterization of axon arborization , 1983, Neuroscience.

[21]  G. Percheron,et al.  A Golgi analysis of the primate globus pallidus. I. Inconstant processes of large neurons, other neuronal types, and afferent axons , 1984, The Journal of comparative neurology.

[22]  W. Nauta,et al.  Afferent and efferent relationships of the basal ganglia. , 1984, Ciba Foundation symposium.

[23]  C. Gerfen.  The neostriatal mosaic: compartmentalization of corticostriatal input and striatonigral output systems , 1984, Nature.

[24]  A. D. Smith,et al.  Characterization of pallidonigral neurons in the rat by a combination of Golgi impregnation and retrograde transport of horseradish peroxidase: their monosynaptic input from the neostriatum , 1984, Journal of neurocytology.

[25]  T. Hattori,et al.  Organization and efferent projections of nucleus tegmenti pedunculopontinus pars compacta with special reference to its cholinergic aspects , 1984, Neuroscience.

[26]  T. F. Freund,et al.  Tyrosine hydroxylase-immunoreactive boutons in synaptic contact with identified striatonigral neurons, with particular reference to dendritic spines , 1984, Neuroscience.

[27]  M. D. Crutcher,et al.  Primate globus pallidus and subthalamic nucleus: functional organization. , 1985, Journal of neurophysiology.

[28]  M. Williams,et al.  The striatonigral projection and nigrotectal neurons in the rat. A correlated light and electron microscopic study demonstrating a monosynaptic striatal input to identified nigrotectal neurons using a combined degeneration and horseradish peroxidase procedure , 1985, Neuroscience.

[29]  W. Nauta,et al.  Efferent connections of the ventral pallidum: Evidence of a dual striato pallidofugal pathway , 1985, The Journal of comparative neurology.

[30]  J. Wu,et al.  Glutamate decarboxylase‐immunoreactive structures in the rat neostriatum: A correlated light and electron microscopic study including a combination of Golgi impregnation with immunocytochemistry , 1985, The Journal of comparative neurology.

[31]  S Afsharpour,et al.  Topographical projections of the cerebral cortex to the subthalamic nucleus , 1985, The Journal of comparative neurology.

[32]  D. Amaral,et al.  The amygdalostriatal projections in the monkey. An anterograde tracing study , 1985, Brain Research.

[33]  C. Gerfen.  The neostriatal mosaic. I. compartmental organization of projections from the striatum to the substantia nigra in the rat , 1985, The Journal of comparative neurology.

[34]  P. Goldman-Rakic,et al.  Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  B. V. Updyke,et al.  Projection of the digit and wrist area of precentral gyrus to the putamen: Relation between topography and physiological properties of neurons in the putamen , 1985, Brain Research.

[36]  C. Hammond,et al.  Stimulation of the subthalamic nucleus enhances the release of dopamine in the rat substantia nigra , 1986, Brain Research.

[37]  Larry L. Butcher,et al.  Cholinergic systems in the rat brain: III. Projections from the pontomesencephalic tegmentum to the thalamus, tectum, basal ganglia, and basal forebrain , 1986, Brain Research Bulletin.

[38]  A. Parent,et al.  Differential connections of caudate nucleus and putamen in the squirrel monkey (Saimiri sciureus) , 1986, Neuroscience.

[39]  R. M. Beckstead,et al.  Striatal axons to the globus pallidus, entopeduncular nucleus and substantia nigra come mainly from separate cell populations in cat , 1986, Neuroscience.

[40]  S. T. Kitai,et al.  The organization of divergent axonal projections from the midbrain raphe nuclei in the rat , 1986, The Journal of comparative neurology.

[41]  K. Chase,et al.  Glutamic acid decarboxylase and enkephalin immunoreactive axon terminals in the rat neostriatum synapse with striatonigral neurons. , 1986, Brain Research.

[42]  M B Hancock,et al.  Two-color immunoperoxidase staining: visualization of anatomic relationships between immunoreactive neural elements. , 1986, The American journal of anatomy.

[43]  J. Price,et al.  Sources of presumptive glutamergic/aspartergic afferents to the rat ventral striatopallidal region , 1987, The Journal of comparative neurology.

[44]  T. Hattori,et al.  Long descending direct projection from the basal ganglia to the spinal cord: a revival of the extrapyramidal concept , 1987, Brain Research.

[45]  G. Percheron,et al.  Spatial Organization and Information Processing in the Core of the Basal Ganglia , 1987 .

[46]  A. Graybiel,et al.  Subdivisions of the dopamine-containing A8-A9-A10 complex identified by their differential mesostriatal innervation of striosomes and extrastriosomal matrix , 1987, Neuroscience.

[47]  M. Delong,et al.  Altered Tonic Activity of Neurons in the Globus Pallidus and Subthalamic Nucleus in the Primate MPTP Model of Parkinsonism , 1987 .

[48]  T. Moriizumi,et al.  Synaptic organization of the cat entopeduncular nucleus with special reference to the relationship between the afferents to entopedunculothalamic projection neurons: An electron microscope study by a combined degeneration and horseradish peroxidase tracing technique , 1987, Neuroscience.

[49]  André Parent,et al.  Neurons of the subthalamic nucleus in primates display glutamate but not GABA immunoreactivity , 1988, Brain Research.

[50]  H. T. Chang.  Substance P-dopamine relationship in the rat substantia nigra: a light and electron microscopy study of double immunocytochemically labeled materials , 1988, Brain Research.

[51]  T. Mahalik.  Direct demonstration of interactions between substance P immunoreactive terminals and tyrosine hydroxylase immunoreactive neurons in the substantia nigra of the rat: An ultrastructural study , 1988, Synapse.

[52]  J. Bolam,et al.  Cholinergic synaptic input to different parts of spiny striatonigral neurons in the rat , 1988, The Journal of comparative neurology.

[53]  A. D. Smith,et al.  Identification of synaptic terminals of thalamic or cortical origin in contact with distinct medium‐size spiny neurons in the rat neostriatum , 1988, The Journal of comparative neurology.

[54]  P. Somogyi,et al.  Synaptic Relationships of Golgi-Impregnated Neurons as Identified by Electrophysiological or Immunocytochemical Techniques , 1989 .

[55]  Y. Smith,et al.  Neurons of the substantia nigra reticulata receive a dense GABA-containing input from the globus pallidus in the rat , 1989, Brain Research.

[56]  L. Descarries,et al.  Serotonin innervation in adult rat neostriatum. II. Ultrastructural features: a radioautographic and immunocytochemical study , 1989, Brain Research.

[57]  O. Bosler,et al.  Ultrastructural correlates of functional relationships between nigral dopaminergic or cortical afferent fibers and neuropeptide Y-containing neurons in the rat striatum , 1989, Neuroscience Letters.

[58]  A. Mcgeorge,et al.  The organization of the projection from the cerebral cortex to the striatum in the rat , 1989, Neuroscience.

[59]  P. Somogyi,et al.  Immunocytochemistry and Synaptic Relationships of Physiologically Characterized HRP-Filled Neurons , 1989 .

[60]  C. Asanuma,et al.  Axonal arborizations of a magnocellular basal nucleus input and their relation to the neurons in the thalamic reticular nucleus of rats. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[61]  Y. Smith,et al.  The output neurones and the dopaminergic neurones of the substantia nigra receive a GABA‐Containing input from the globus pallidus in the rat , 1990, The Journal of comparative neurology.

[62]  B. Bloch,et al.  Dopamine receptor gene expression by enkephalin neurons in rat forebrain. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[63]  V. Pickel,et al.  Spiny neurons lacking choline acetyltransferase immunoreactivity are major targets of cholinergic and catecholaminergic terminals in rat striatum , 1990, Journal of neuroscience research.

[64]  Y. Smith,et al.  Topographical and Synaptic Organization of the GABA‐Containing Pallidosubthalamic Projection in the Rat , 1990, The European journal of neuroscience.

[65]  A. Parent,et al.  Efferent projections of the subthalamic nucleus in the squirrel monkey as studied by the PHA‐L anterograde tracing method , 1990, The Journal of comparative neurology.

[66]  C. Asanuma,et al.  Light and electron microscopic evidence for a GABAergic projection from the caudal basal forebrain to the thalamic reticular nucleus in rats , 1990, The Journal of comparative neurology.

[67]  N. Canteras,et al.  Afferent connections of the subthalamic nucleus: a combined retrograde and anterograde horseradish peroxidase study in the rat , 1990, Brain Research.

[68]  S. Haber,et al.  Evidence for interconnections between the two segments of the globus pallidus in primates: a PHA-L anterograde tracing study , 1990, Brain Research.

[69]  A. Parent.  Extrinsic connections of the basal ganglia , 1990, Trends in Neurosciences.

[70]  H. Bergman,et al.  Reversal of experimental parkinsonism by lesions of the subthalamic nucleus. , 1990, Science.

[71]  A. D. Smith,et al.  The neural network of the basal ganglia as revealed by the study of synaptic connections of identified neurones , 1990, Trends in Neurosciences.

[72]  H. Groenewegen,et al.  Connections of the subthalamic nucleus with ventral striatopallidal parts of the basal ganglia in the rat , 1990, The Journal of comparative neurology.

[73]  A. Graybiel.  Neurotransmitters and neuromodulators in the basal ganglia , 1990, Trends in Neurosciences.

[74]  H. Kita,et al.  Amygdaloid projections to the frontal cortex and the striatum in the rat , 1990, The Journal of comparative neurology.

[75]  C. Wilson,et al.  Projection subtypes of rat neostriatal matrix cells revealed by intracellular injection of biocytin , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[76]  A. Parent,et al.  Immunohistochemical study of the serotoninergic innervation of the basal ganglia in the squirrel monkey , 1990, The Journal of comparative neurology.

[77]  A. Crossman,et al.  A hypothesis on the pathophysiological mechanisms that underlie levodopa‐ or dopamine agonist‐induced dyskinesia in Parkinson's disease: Implications for future strategies in treatment , 1990, Movement disorders : official journal of the Movement Disorder Society.

[78]  A. Parent,et al.  Projection from the external pallidum to the reticular thalamic nucleus in the squirrel monkey , 1991, Brain Research.

[79]  Y. Smith,et al.  Convergence of synaptic inputs from the striatum and the globus pallidus onto identified nigrocollicular cells in the rat: A double anterograde labelling study , 1991, Neuroscience.

[80]  A. McDonald,et al.  Topographical organization of amygdaloid projections to the caudatoputamen, nucleus accumbens, and related striatal-like areas of the rat brain , 1991, Neuroscience.

[81]  H. Kita,et al.  Intracellular study of rat globus pallidus neurons: membrane properties and responses to neostriatal, subthalamic and nigral stimulation , 1991, Brain Research.

[82]  B. Bloch,et al.  Phenotypical characterization of the rat striatal neurons expressing the D1 dopamine receptor gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[83]  Henk J. Groenewegen,et al.  The Connections of the Medial Part of the Subthalamic Nucleus in the Rat: Evidence for a Parallel Organization , 1991 .

[84]  H. Kita,et al.  Intracellular study of rat entopeduncular nucleus neurons in an in vitro slice preparation: response to subthalamic stimulation , 1991, Brain Research.

[85]  A. McDonald,et al.  Organization of amygdaloid projections to the prefrontal cortex and associated striatum in the rat , 1991, Neuroscience.

[86]  P. Izzo.  A note on the use of biocytin in anterograde tracing studies in the central nervous system: Application at both light and electron microscopic level , 1991, Journal of Neuroscience Methods.

[87]  P. Emson,et al.  Restoration of thalamostriatal projections in rat neostriatal grafts: An electron microscopic analysis , 1991, The Journal of comparative neurology.

[88]  D. Pandya,et al.  Prefrontostriatal connections in relation to cortical architectonic organization in rhesus monkeys , 1991, The Journal of comparative neurology.

[89]  J. Penney,et al.  Evidence for a projection from the globus pallidus to the entopeduncular nucleus in the rat , 1991, Neuroscience Letters.

[90]  W. T. Thach,et al.  Basal ganglia motor control. II. Late pallidal timing relative to movement onset and inconsistent pallidal coding of movement parameters. , 1991, Journal of neurophysiology.

[91]  W. T. Thach,et al.  Basal ganglia motor control. I. Nonexclusive relation of pallidal discharge to five movement modes. , 1991, Journal of neurophysiology.

[92]  Y. Smith,et al.  Synaptic organization of gabaergic inputs from the striatum and the globus pallidus onto neurons in the substantia nigra and retrorubral field which project to the medullary reticular formation , 1992, Neuroscience.

[93]  André Parent,et al.  Convergence of subthalamic and striatal efferents at pallidal level in primates: an anterograde double-labeling study with biocytin and PHA-L , 1992, Brain Research.

[94]  S. Henriksen,et al.  Electrophysiological evidence for reciprocal connectivity between the nucleus accumbens septi and ventral pallidal region , 1992, Brain Research.

[95]  U. Eysel,et al.  Cellular organization of reciprocal patchy networks in layer III of cat visual cortex (area 17) , 1992, Neuroscience.

[96]  H. Groenewegen,et al.  Topographical organization and relationship with ventral striatal compartments of prefrontal corticostriatal projections in the rat , 1992, The Journal of comparative neurology.

[97]  H. Kita.  Responses of globus pallidus neurons to cortical stimulation: intracellular study in the rat , 1992, Brain Research.

[98]  S. Sesack,et al.  Cellular basis for interactions between catecholaminergic afferents and neurons containing leu‐enkephalin‐like immunoreactivity in rat caudate‐putamen nuclei , 1992, Journal of neuroscience research.

[99]  D. S. Zahm,et al.  On the significance of subterritories in the “accumbens” part of the rat ventral striatum , 1992, Neuroscience.

[100]  A. Vania Apkarian,et al.  Biotin-dextran: a sensitive anterograde tracer for neuroanatomic studies in rat and monkey , 1992, Journal of Neuroscience Methods.

[101]  C. Gerfen.  The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia. , 1992, Annual review of neuroscience.

[102]  M. Hariz,et al.  Leksell's posteroventral pallidotomy in the treatment of Parkinson's disease. , 1992, Journal of neurosurgery.

[103]  A. Grace,et al.  Role of the subthalamic nucleus in the regulation of nigral dopamine neuron activity , 1992, Synapse.

[104]  B. Bloch,et al.  Phenotypical characterization of the rat striatal neurons expressing muscarinic receptor genes , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[105]  M R DeLong,et al.  Excitotoxic acid lesions of the primate subthalamic nucleus result in transient dyskinesias of the contralateral limbs. , 1992, Journal of neurophysiology.

[106]  C. Geula,et al.  Cholinergic innervation of the human striatum, globus pallidus, subthalamic nucleus, substantia nigra, and red nucleus , 1992, The Journal of comparative neurology.

[107]  M. Delong,et al.  Excitotoxic acid lesions of the primate subthalamic nucleus result in reduced pallidal neuronal activity during active holding. , 1992, Journal of neurophysiology.

[108]  A. Parent,et al.  Cortical input to parvalbumin-immunoreactive neurones in the putamen of the squirrel monkey , 1992, Brain Research.

[109]  A. Parent,et al.  Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: A PHA‐L study of subcortical projections , 1992, The Journal of comparative neurology.

[110]  J. Bolam,et al.  Input from the frontal cortex and the parafascicular nucleus to cholinergic interneurons in the dorsal striatum of the rat , 1992, Neuroscience.

[111]  A. Nieoullon,et al.  Cellular interactions in the striatum involving neuronal systems using “classical” neurotransmitters: Possible functional implications , 1992, Movement disorders : official journal of the Movement Disorder Society.

[112]  A. Parent,et al.  The striatopallidal projection displays a high degree of anatomical specificity in the primate , 1992, Brain Research.

[113]  K. Clark,et al.  Auto- and cross-correlation analysis of subthalamic nucleus neuronal activity in neostriatal- and globus pallidal-lesioned rats , 1992, Brain Research.

[114]  H. Kita,et al.  GABAergic circuits of the striatum. , 1993, Progress in brain research.

[115]  W. T. Thach,et al.  Basal ganglia intrinsic circuits and their role in behavior , 1993, Current Opinion in Neurobiology.

[116]  P. Strick,et al.  Multiple output channels in the basal ganglia. , 1993, Science.

[117]  D. S. Zahm,et al.  The patterns of afferent innervation of the core and shell in the “Accumbens” part of the rat ventral striatum: Immunohistochemical detection of retrogradely transported fluoro‐gold , 1993, The Journal of comparative neurology.

[118]  B Bioulac,et al.  Reversal of Rigidity and Improvement in Motor Performance by Subthalamic High‐frequency Stimulation in MPTP‐treated Monkeys , 1993, The European journal of neuroscience.

[119]  N. Rajakumar,et al.  Biotinylated dextran: a versatile anterograde and retrograde neuronal tracer , 1993, Brain Research.

[120]  I. Llewellyn-Smith,et al.  The tungstate-stabilized tetramethylbenzidine reaction for light and electron microscopic immunocytochemistry and for revealing biocytin-filled neurons , 1993, Journal of Neuroscience Methods.

[121]  A. Parent,et al.  Anatomical aspects of information processing in primate basal ganglia , 1993, Trends in Neurosciences.

[122]  M. Mouroux,et al.  Evidence that the parafascicular projection to the subthalamic nucleus is glutamatergic. , 1993, Neuroreport.

[123]  T. Klockgether,et al.  Toward an understanding of the role of glutamate in experimental parkinsonism: Agonist‐sensitive sites in the basal ganglia , 1993, Annals of neurology.

[124]  S. Haber,et al.  The organization of the descending ventral pallidal projections in the monkey , 1993, The Journal of comparative neurology.

[125]  Y. Smith,et al.  Convergence of synaptic terminals from the striatum and the globus pallidus onto single neurones in the substantia nigra and the entopeduncular nucleus. , 1993, Progress in brain research.

[126]  Floris G. Wouterlood,et al.  The anterograde neuroanatomical tracer biotinylated dextran-amine: comparison with the tracer Phaseolus vulgaris-leucoagglutinin in preparations for electron microscopy , 1993, Journal of Neuroscience Methods.

[127]  A. Burkhalter,et al.  Visualization of dendritic morphology of cortical projection neurons by retrograde axonal tracing , 1993, Journal of Neuroscience Methods.

[128]  H. Kita,et al.  Response characteristics of subthalamic neurons to the stimulation of the sensorimotor cortex in the rat , 1993, Brain Research.

[129]  S. D. L. Heras,et al.  Afferent projections to the reticular thalamic nucleus from the globus pallidus and the substantia nigra in the rat , 1993, Brain Research Bulletin.

[130]  O. Ottersen,et al.  Terminals of subthalamonigral fibres are enriched with glutamate-like immunoreactivity: An electron microscopic, immunogold analysis in the cat , 1993, Journal of Chemical Neuroanatomy.

[131]  A. Cools,et al.  Descending efferent connections of the sub‐pallidal areas in the cat: Projections to the subthalamic nucleus, the hypothalamus, and the midbrain , 1993, Synapse.

[132]  H. Kita,et al.  The morphology of globus pallidus projection neurons in the rat: an intracellular staining study , 1994, Brain Research.

[133]  M R DeLong,et al.  The primate subthalamic nucleus. III. Changes in motor behavior and neuronal activity in the internal pallidum induced by subthalamic inactivation in the MPTP model of parkinsonism. , 1994, Journal of neurophysiology.

[134]  S. Haber,et al.  Primate cingulostriatal projection: Limbic striatal versus sensorimotor striatal input , 1994, The Journal of comparative neurology.

[135]  L. Ryan,et al.  Subthalamic nucleus and globus pallidus lesions alter activity in nigrothalamic neurons in rats , 1994, Brain Research Bulletin.

[136]  A. Parent,et al.  Synaptic relationships between dopaminergic afferents and cortical or thalamic input in the sensorimotor territory of the striatum in monkey , 1994, The Journal of comparative neurology.

[137]  S. Haber,et al.  Integrative Aspects of Basal Ganglia Circuitry , 1994 .

[138]  C. Wilson,et al.  Spontaneous firing patterns and axonal projections of single corticostriatal neurons in the rat medial agranular cortex. , 1994, Journal of neurophysiology.

[139]  A. Parent,et al.  Pedunculopontine nucleus in the squirrel monkey: Projections to the basal ganglia as revealed by anterograde tract‐tracing methods , 1994, The Journal of comparative neurology.

[140]  N. Rajakumar,et al.  The pallidostriatal projection in the rat: a recurrent inhibitory loop? , 1994, Brain Research.

[141]  T. Wichmann,et al.  Synaptic innervation of neurons in the internal pallidal segment by the subthalamic nucleus and the external pallidum in monkeys , 1994, The Journal of comparative neurology.

[142]  E. Scarnati,et al.  Regulatory Action of the Dopaminergic Nigrostriatal Pathway on the Corticostriatal Transmission , 1994 .

[143]  B. D. Bennett,et al.  Synaptic input and output of parvalbumin-immunoreactive neurons in the neostriatum of the rat , 1994, Neuroscience.

[144]  M. Bevan,et al.  The projections from the parafascicular thalamic nucleus to the subthalamic nucleus and the striatum arise from separate neuronal populations: A comparison with the corticostriatal and corticosubthalamic efferents in a retrograde fluorescent double-labelling study , 1994, Neuroscience.

[145]  D. Joel,et al.  The organization of the basal ganglia-thalamocortical circuits: Open interconnected rather than closed segregated , 1994, Neuroscience.

[146]  A M Graybiel,et al.  The basal ganglia and adaptive motor control. , 1994, Science.

[147]  T. Wichmann,et al.  The External Pallidum and the Subthalamic Nucleus Send Convergent Synaptic Inputs onto Single Neurones in the Internal Pallidal Segment in Monkey:Anatomical Organization and Functional Significance , 1994 .

[148]  S. Hernández,et al.  Activation of subthalamic neurons produces NMDA receptor-mediated dendritic dopamine release in substantia nigra pars reticulata: a microdialysis study in the rat , 1994, Brain Research.

[149]  D. Surmeier,et al.  Dopaminergic regulation of striatal efferent pathways , 1994, Current Opinion in Neurobiology.

[150]  Charles J. Wilson,et al.  Striatal interneurones: chemical, physiological and morphological characterization , 1995, Trends in Neurosciences.

[151]  M. Starr.  Antiparkinsonian actions of glutamate antagonists — alone and with L-DOPA: A review of evidence and suggestions for possible mechanisms , 1995, Journal of neural transmission. Parkinson's disease and dementia section.

[152]  M. Delong,et al.  Parkinson's Disease and the Basal Ganglia: Lessons from the Laboratory and from Neurosurgery , 1995 .

[153]  J. Bolam,et al.  The glutamate‐enriched cortical and thalamic input to neurons in the subthalamic nucleus of the rat: Convergence with GABA‐positive terminals , 1995, The Journal of comparative neurology.

[154]  A. Parent,et al.  Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop , 1995, Brain Research Reviews.

[155]  J. Dostrovsky,et al.  Effect of GPi pallidotomy on motor function in Parkinson's disease , 1995, The Lancet.

[156]  J. Bolam,et al.  Electron microscopic analysis of D1 and D2 dopamine receptor proteins in the dorsal striatum and their synaptic relationships with motor corticostriatal afferents , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[157]  Y. Smith,et al.  Differential synaptic innervation of neurons in the internal and external segments of the globus pallidus by the GABA‐ and glutamate‐containing terminals in the squirrel monkey , 1995, The Journal of comparative neurology.

[158]  O. Hassani,et al.  Electrophysiological study of the excitatory parafascicular projection to the subthalamic nucleus and evidence for ipsi- and contralateral controls , 1995, Neuroscience.

[159]  E. Lynd-Balta,et al.  The orbital and medial prefrontal circuit through the primate basal ganglia , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[160]  A. Parent,et al.  Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidium in basal ganglia circuitry , 1995, Brain Research Reviews.

[161]  Y. Smith,et al.  Differential synaptic innervation of striatofugal neurones projecting to the internal or external segments of the globus pallidus by thalamic afferents in the squirrel monkey , 1996, The Journal of comparative neurology.

[162]  L. Heimer,et al.  Efferent connections of the caudal part of the globus pallidus in the rat , 1996, The Journal of comparative neurology.

[163]  C. Wilson,et al.  Corticostriatal innervation of the patch and matrix in the rat neostriatum , 1996, The Journal of comparative neurology.

[164]  Y. Smith,et al.  The subthalamic nucleus and the external pallidum: two tightly interconnected structures that control the output of the basal ganglia in the monkey , 1996, Neuroscience.

[165]  A. D. Smith,et al.  The substantia nigra as a site of synaptic integration of functionally diverse information arising from the ventral pallidum and the globus pallidus in the rat , 1996, Neuroscience.

[166]  D. Paré,et al.  Thalamic collaterals of corticostriatal axons: Their termination field and synaptic targets in cats , 1996, The Journal of comparative neurology.

[167]  S. Haber,et al.  Ventral pallidostriatal pathway in the monkey: evidence for modulation of basal ganglia circuits. , 1996, The Journal of comparative neurology.

[168]  D. Oorschot.  Total number of neurons in the neostriatal, pallidal, subthalamic, and substantia nigral nuclei of the rat basal ganglia: A stereological study using the cavalieri and optical disector methods , 1996, The Journal of comparative neurology.

[169]  M. Inase,et al.  Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplementary motor area , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[170]  B Bioulac,et al.  Alleviation of experimental hemiparkinsonism by high‐frequency stimulation of the subthalamic nucleus in primates: A comparison with L‐dopa treatment , 1996, Movement disorders : official journal of the Movement Disorder Society.

[171]  J. Walters,et al.  Apomorphine and dopamine D1 receptor agonists increase the firing rates of subthalamic nucleus neurons , 1996, Neuroscience.

[172]  D. Surmeier,et al.  Coordinated Expression of Dopamine Receptors in Neostriatal Medium Spiny Neurons , 1996, The Journal of Neuroscience.

[173]  J. Mink.  THE BASAL GANGLIA: FOCUSED SELECTION AND INHIBITION OF COMPETING MOTOR PROGRAMS , 1996, Progress in Neurobiology.

[174]  J. Bolam,et al.  Glutamate‐enriched Inputs from the Mesopontine Tegmentum to the Entopeduncular Nucleus in the Rat , 1996, The European journal of neuroscience.

[175]  M. Delong,et al.  Functional and pathophysiological models of the basal ganglia , 1996, Current Opinion in Neurobiology.

[176]  S. Consolo,et al.  The Cerebral Cortex and Parafascicular Thalamic Nucleus Facilitate In vivo Acetylcholine Release in the Rat Striatum through Distinct Glutamate Receptor Subtypes , 1996, The European journal of neuroscience.

[177]  R. Turner,et al.  Treatment of advanced Parkinson's disease by posterior GPi pallidotomy: 1‐year results of a pilot study , 1996, Annals of neurology.

[178]  M. Deschenes,et al.  Corticostriatal projections from layer V cells in rat are collaterals of long-range corticofugal axons , 1996, Brain Research.

[179]  Y. Smith,et al.  Efferent connections of the internal globus pallidus in the squirrel monkey: I. topography and synaptic organization of the pallidothalamic projection , 1997, The Journal of comparative neurology.

[180]  Peter Dayan,et al.  A Neural Substrate of Prediction and Reward , 1997, Science.

[181]  Richard S. J. Frackowiak,et al.  Changes in cerebral activity pattern due to subthalamic nucleus or internal pallidum stimulation in Parkinson's disease , 1997, Annals of neurology.

[182]  L. Heimer,et al.  Substantia innominata: a notion which impedes clinical–anatomical correlations in neuropsychiatric disorders , 1997, Neuroscience.

[183]  A M Graybiel,et al.  Cortically Driven Immediate-Early Gene Expression Reflects Modular Influence of Sensorimotor Cortex on Identified Striatal Neurons in the Squirrel Monkey , 1997, The Journal of Neuroscience.

[184]  Atsushi Nambu,et al.  Morphology of globus pallidus neurons: Its correlation with electrophysiology in guinea pig brain slices , 1997, The Journal of comparative neurology.

[185]  Sylvain Houle,et al.  Globus pallidus stimulation activates the cortical motor system during alleviation of parkinsonian symptoms , 1997, Nature Medicine.

[186]  O. Hassani,et al.  Evidence for a dopaminergic innervation of the subthalamic nucleus in the rat , 1997, Brain Research.

[187]  O. Hassani,et al.  Re-evaluation of the functional anatomy of the basal ganglia in normal and Parkinsonian states , 1997, Neuroscience.

[188]  P. Calabresi,et al.  The neostriatum beyond the motor function: experimental and clinical evidence. , 1997, Neuroscience.

[189]  Y. Smith,et al.  Efferent connections of the internal globus pallidus in the squirrel monkey: II. topography and synaptic organization of pallidal efferents to the pedunculopontine nucleus , 1997, The Journal of comparative neurology.

[190]  E. Vaadia,et al.  Physiological aspects of information processing in the basal ganglia of normal and parkinsonian primates , 1998, Trends in Neurosciences.

[191]  M. Merello,et al.  [Functional anatomy of the basal ganglia]. , 2000, Revista de neurologia.

[192]  R. Goodman.  Surgery for Parkinson's Disease , 2019, Cambridge International Law Journal.