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      The Cortico-Basal Ganglia-Cerebellar Network: Past, Present and Future Perspectives

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          Abstract

          Much of our present understanding of the function and operation of the basal ganglia rests on models of anatomical connectivity derived from tract-tracing approaches in rodents and primates. However, the last years have been characterized by promising step forwards in the in vivo investigation and comprehension of brain connectivity in humans. The aim of this review is to revise the current knowledge on basal ganglia circuits, highlighting similarities and differences across species, in order to widen the current perspective on the intricate model of the basal ganglia system. This will allow us to explore the implications of additional direct pathways running from cortex to basal ganglia and between basal ganglia and cerebellum recently described in animals and humans.

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          Most cited references115

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          Robust determination of the fibre orientation distribution in diffusion MRI: non-negativity constrained super-resolved spherical deconvolution.

          Diffusion-weighted (DW) MR images contain information about the orientation of brain white matter fibres that potentially can be used to study human brain connectivity in vivo using tractography techniques. Currently, the diffusion tensor model is widely used to extract fibre directions from DW-MRI data, but fails in regions containing multiple fibre orientations. The spherical deconvolution technique has recently been proposed to address this limitation. It provides an estimate of the fibre orientation distribution (FOD) by assuming the DW signal measured from any fibre bundle is adequately described by a single response function. However, the deconvolution is ill-conditioned and susceptible to noise contamination. This tends to introduce artefactual negative regions in the FOD, which are clearly physically impossible. In this study, the introduction of a constraint on such negative regions is proposed to improve the conditioning of the spherical deconvolution. This approach is shown to provide FOD estimates that are robust to noise whilst preserving angular resolution. The approach also permits the use of super-resolution, whereby more FOD parameters are estimated than were actually measured, improving the angular resolution of the results. The method provides much better defined fibre orientation estimates, and allows orientations to be resolved that are separated by smaller angles than previously possible. This should allow tractography algorithms to be designed that are able to track reliably through crossing fibre regions.
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            What makes us tick? Functional and neural mechanisms of interval timing.

            Time is a fundamental dimension of life. It is crucial for decisions about quantity, speed of movement and rate of return, as well as for motor control in walking, speech, playing or appreciating music, and participating in sports. Traditionally, the way in which time is perceived, represented and estimated has been explained using a pacemaker-accumulator model that is not only straightforward, but also surprisingly powerful in explaining behavioural and biological data. However, recent advances have challenged this traditional view. It is now proposed that the brain represents time in a distributed manner and tells the time by detecting the coincidental activation of different neural populations.
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              Perisylvian language networks of the human brain.

              Early anatomically based models of language consisted of an arcuate tract connecting Broca's speech and Wernicke's comprehension centers; a lesion of the tract resulted in conduction aphasia. However, the heterogeneous clinical presentations of conduction aphasia suggest a greater complexity of perisylvian anatomical connections than allowed for in the classical anatomical model. This article re-explores perisylvian language connectivity using in vivo diffusion tensor magnetic resonance imaging tractography. Diffusion tensor magnetic resonance imaging data from 11 right-handed healthy male subjects were averaged, and the arcuate fasciculus of the left hemisphere reconstructed from this data using an interactive dissection technique. Beyond the classical arcuate pathway connecting Broca's and Wernicke's areas directly, we show a previously undescribed, indirect pathway passing through inferior parietal cortex. The indirect pathway runs parallel and lateral to the classical arcuate fasciculus and is composed of an anterior segment connecting Broca's territory with the inferior parietal lobe and a posterior segment connecting the inferior parietal lobe to Wernicke's territory. This model of two parallel pathways helps explain the diverse clinical presentations of conduction aphasia. The anatomical findings are also relevant to the evolution of language, provide a framework for Lichtheim's symptom-based neurological model of aphasia, and constrain, anatomically, contemporary connectionist accounts of language.
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                Author and article information

                Contributors
                Journal
                Front Syst Neurosci
                Front Syst Neurosci
                Front. Syst. Neurosci.
                Frontiers in Systems Neuroscience
                Frontiers Media S.A.
                1662-5137
                30 October 2019
                2019
                : 13
                : 61
                Affiliations
                [1] 1Department of Biomedical, Dental Sciences and Morphological and Functional Images, University of Messina , Messina, Italy
                [2] 2IRCCS Centro Neurolesi “Bonino Pulejo” , Messina, Italy
                [3] 3I.S.A.S.I.E. Caianello, National Research Council , Messina, Italy
                Author notes

                Edited by: Preston E. Garraghty, Indiana University Bloomington, United States

                Reviewed by: Martin Bares, Masaryk University, Czechia; Ellen J. Hess, Emory University, United States; Kate Roman, Emory University, Unites States, in collaboration with reviewer EH

                *Correspondence: Angelo Quartarone aquartar65@ 123456gmail.com Alberto Cacciola alberto.cacciola0@ 123456gmail.com

                These authors have contributed equally to this work

                Article
                10.3389/fnsys.2019.00061
                6831548
                31736719
                dc5f7f43-5e13-4312-9916-44c2701682c8
                Copyright © 2019 Milardi, Quartarone, Bramanti, Anastasi, Bertino, Basile, Buonasera, Pilone, Celeste, Rizzo, Bruschetta and Cacciola.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 23 April 2019
                : 08 October 2019
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 150, Pages: 14, Words: 12042
                Categories
                Neuroscience
                Review

                Neurosciences
                cerebellum,connectomics,globus pallidus,substantia nigra,tractography
                Neurosciences
                cerebellum, connectomics, globus pallidus, substantia nigra, tractography

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