Subcortical Aphasia: An Update.
Basal ganglia
Connectivity studies
Neuroimaging
Subcortical aphasia
Thalamus
Tractography
Journal
Current neurology and neuroscience reports
ISSN: 1534-6293
Titre abrégé: Curr Neurol Neurosci Rep
Pays: United States
ID NLM: 100931790
Informations de publication
Date de publication:
11 Sep 2024
11 Sep 2024
Historique:
accepted:
19
08
2024
medline:
11
9
2024
pubmed:
11
9
2024
entrez:
11
9
2024
Statut:
aheadofprint
Résumé
This review aims to rediscuss the leading theories concerning the role of basal ganglia and the thalamus in the genesis of aphasic symptoms in the absence of gross anatomical lesions in cortical language areas as assessed by conventional neuroimaging studies. New concepts in language processing and modern neuroimaging techniques have enabled some progress in resolving the impasse between the current dominant theories: (a) direct and specific linguistic processing and (b) subcortical structures as processing relays in domain-general functions. Of particular interest are studies of connectivity based on functional magnetic resonance imaging (MRI) and tractography that highlight the impact of white matter pathway lesions on aphasia development and recovery. Connectivity studies have put into evidence the central role of the arcuate fasciculus (AF), inferior frontal occipital fasciculus (IFOF), and uncinate fasciculus (UF) in the genesis of aphasia. Regarding the thalamus, its involvement in lexical-semantic processing through modulation of the frontal cortex is becoming increasingly apparent.
Identifiants
pubmed: 39259429
doi: 10.1007/s11910-024-01373-8
pii: 10.1007/s11910-024-01373-8
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Références
Broca P. Siège De La faculté Du langage articulé. Perte de la parole. Ramollissement Chronique Et destruction Partielle Du lobe antèrieur Gauche Du Cervau. Bull Soc Anthropol. 1861;2:235. French.
Wernicke C. Der Aphasische Symptomencomplex. Breslau: Cohn & Weigert; 1874. German.
Lichtheim L. On aphasia. Brain. 1885;7:433–84.
doi: 10.1093/brain/7.4.433
Broadbent WH. On the cerebral mechanism of speech and thought. Med Chir Trans. 1872;55:145–94.
pubmed: 20896383
pmcid: 2150499
doi: 10.1177/095952877205500108
Kussmaul A. Disturbances of speech. Cyclopedie Pract Med. 1877;14:581.
Marie P. The third left frontal convolution plays no special role in the function of language. Semaine Médicale. 1906;26:241–47. French.
Von Monakow C. Die Lokalisation in Grosshirn. Wiesbaden: Bergmann; 1914.
Dejerine J. L’aphasie motrice: sa localisation et sa physiologie pathologique. Presse Médicale. 1906;57:453–57. French.
Samra K, Riklan M, Levita E, Zimmerman J, Waltz JM, Bergmann L, Cooper IS. Language and speech correlates of anatomically verified lesions in thalamic surgery for parkinsonism. J Speech Hear Res. 1969;12:510–40.
pubmed: 4897811
doi: 10.1044/jshr.1203.510
Darley FL, Brown JR, Swenson WM. Language changes after neurosurgery for parkinsonism. Brain Lang. 1975;2:65–9.
pubmed: 1164668
doi: 10.1016/S0093-934X(75)80054-X
Ojemann GA. Language and the thalamus: object naming and recall during and after thalamic stimulation. Brain Lang. 1975;2:101–20.
pubmed: 1100194
doi: 10.1016/S0093-934X(75)80057-5
Penfield W, Roberts L. Speech and brain mechanisms. Princeton: Princeton Univ. Press; 1959.
Schuell H, Jenkins JJ, Jimenez-Pabon E. Aphasia in adults. New York: Harper & Row; 1965.
Crosson B. Subcortical functions in language: a working model. Brain Lang. 1985;25:257–92.
pubmed: 3904918
doi: 10.1016/0093-934X(85)90085-9
Alexander GE, DeLong MR, Strick PL. Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu Rev Neurosci. 1986;9:357–81.
pubmed: 3085570
doi: 10.1146/annurev.ne.09.030186.002041
Copland DA, Brownsett S, Iyer K, Angwin AJ. Corticostriatal Regulation of Language Functions. Neuropsychol Rev. 2021;31:472–494.** In this review, the authors argue for a domain-general regulatory role of corticostriatal systems in language tasks involving uncertainty or conflict and which demand selection, sequencing, and cognitive control.
Frank MJ. Hold your horses: a dynamic computational role for the subthalamic nucleus in decision making. Neural Netw. 2006;19:1120–36.
pubmed: 16945502
doi: 10.1016/j.neunet.2006.03.006
Houk JC, Bastianen C, Fansler D, Fishbach A, Fraser D, Reber PJ, Roy SA, Simo LS. Action selection and refinement in subcortical loops through basal ganglia and cerebellum. Philos Trans R Soc Lond B Biol Sci. 2007;362:1573–83.
pubmed: 17428771
pmcid: 2440782
doi: 10.1098/rstb.2007.2063
Damasio AR, Damasio H, Rizzo M, Varney N, Gersh F. Aphasia with nonhemorrhagic lesions in the basal ganglia and internal capsule. Arch Neurol. 1982;39:15–24.
pubmed: 7055442
doi: 10.1001/archneur.1982.00510130017003
Naeser MA, Alexander MP, Helm-Estabrooks N, Levine HL, Laughlin SA, Geschwind N. Aphasia with predominantly subcortical lesion sites: description of three capsular/putaminal aphasia syndromes. Arch Neurol. 1982;39:2–14.
pubmed: 6976780
doi: 10.1001/archneur.1982.00510130004002
Cappa SF, Cavallotti G, Guidotti M, Papagno C, Vignolo LA. Subcortical aphasia: two clinical-CT scan correlation studies. Cortex. 1983;19:227–41.
pubmed: 6192970
doi: 10.1016/S0010-9452(83)80016-1
Mega MS, Alexander MP. Subcortical aphasia: the core profile of capsulostriatal infarction. Neurology. 1994;44:1824–9.
pubmed: 7936230
doi: 10.1212/WNL.44.10.1824
Wallesch CW, Papagno C. Subcortical aphasia. In: Rose FC, Whurr R, Wyke MA, editors. Aphasia. London: Whurr; 1988.
Crosson B, Benefield H, Cato MA, Sadek JR, Moore AB, Wierenga CE, Gopinath K, Soltysik D, Bauer RM, Auerbach EJ, Gökçay D, Leonard CM, Briggs RW. Left and right basal ganglia and frontal activity during language generation: contributions to lexical, semantic, and phonological processes. J Int Neuropsychol Soc. 2003;9:1061–77.
pubmed: 14738287
doi: 10.1017/S135561770397010X
Longworth CE, Keenan SE, Barker RA, Marslen-Wilson WD, Tyler LK. The basal ganglia and rule-governed language use: evidence from vascular and degenerative conditions. Brain. 2005;128:584–96.
pubmed: 15659423
doi: 10.1093/brain/awh387
Camerino I, Ferreira J, Vonk JM, Kessels RPC, de Leeuw FE, Roelofs A, Copland D, Piai V. Systematic Review and Meta-Analyses of Word Production Abilities in Dysfunction of the Basal Ganglia: Stroke, Small Vessel Disease, Parkinson’s Disease, and Huntington’s Disease. Neuropsychol Rev. 2024;34:1–26.*A meta-analysis of 114 studies addressing word production tasks in vascular and non-vascular pathologies of the basal ganglia.
Inase M, Tokuno H, Nambu A, Akazawa T, Takada M. Corticostriatal and corticosubthalamic input zones from the presupplementary motor area in the macaque monkey: comparison with the input zones from the supplementary motor area. Brain Res. 1999;833:191–201.
pubmed: 10375694
doi: 10.1016/S0006-8993(99)01531-0
Martnez-Sánchez F. Trastornos Del habla y la voz en la enfermedad de Parkinson [Speech and voice disorders in Parkinson’s disease]. Rev Neurol. 2010;51:542–50. Spanish.
pubmed: 20979034
Bhatia KP, Marsden CD. The behavioural and motor consequences of focal lesions of the basal ganglia in man. Brain. 1994;117:859–76.
pubmed: 7922471
doi: 10.1093/brain/117.4.859
Kotz SA, Schwartze M. Cortical speech processing unplugged: a timely subcortico-cortical framework. Trends Cogn Sci. 2010;14:392–9.
pubmed: 20655802
doi: 10.1016/j.tics.2010.06.005
Kemmerer D. Prosody. In: Kemmerer D, editor Cognitive neuroscience of language.2015; New York, NY: Psychology.
Kotz SA, Frisch S, von Cramon DY, Friederici AD. Syntactic language processing: ERP lesion data on the role of the basal ganglia. J Int Neuropsychol Soc. 2003;9:1053–60.
pubmed: 14738286
doi: 10.1017/S1355617703970093
Ullman MT, Pancheva R, Love T, Yee E, Swinney D, Hickok G. Neural correlates of lexicon and grammar: evidence from the production, reading, and judgment of inflection in aphasia. Brain Lang. 2005;93:185–238. discussion 239 – 42.
pubmed: 15781306
doi: 10.1016/j.bandl.2004.10.001
Dominey PF, Inui T. Cortico-striatal function in sentence comprehension: insights from neurophysiology and modeling. Cortex. 2009;45:1012–8.
pubmed: 19446801
doi: 10.1016/j.cortex.2009.03.007
Teichmann M, Rosso C, Martini JB, Bloch I, Brugières P, Duffau H, Lehéricy S, Bachoud-Lévi AC. A cortical-subcortical syntax pathway linking Broca’s area and the striatum. Hum Brain Mapp. 2015;36:2270–83.
pubmed: 25682763
pmcid: 6869141
doi: 10.1002/hbm.22769
Lieberman RR, Ellenberg M, Restum WH. Aphasia associated with verified subcortical lesions: three case reports. Arch Phys Med Rehabil. 1986;67:410–4.
pubmed: 2424402
Alexander MP, Naeser MA, Palumbo CL. Correlations of subcortical CT lesion sites and aphasia profiles. Brain. 1987;110:961–91.
pubmed: 3651803
doi: 10.1093/brain/110.4.961
Naeser MA, Palumbo CL, Helm-Estabrooks N, Stiassny-Eder D, Albert ML. Severe nonfluency in aphasia. Role of the medial subcallosal fasciculus and other white matter pathways in recovery of spontaneous speech. Brain. 1989;112:1–38.
pubmed: 2917272
doi: 10.1093/brain/112.1.1
Nadeau SE. Subcortical language mechanisms. In Stemmer B, Whitaker HA, editors, Handbook of the neuroscience of language.2008.Pp. 329–40.London, UK: Academic.
Hickok G, Poeppel D. The cortical organization of speech processing. Nat Rev Neurosci. 2007;8:393–402.
pubmed: 17431404
doi: 10.1038/nrn2113
Catani M, Jones DK, ffytche DH. Perisylvian language networks of the human brain. Ann Neurol. 2005;57:8–16.
pubmed: 15597383
doi: 10.1002/ana.20319
Baboyan V, Basilakos A, Yourganov G, Rorden C, Bonilha L, Fridriksson J, Hickok G. Isolating the white matter circuitry of the dorsal language stream: Connectome-Symptom Mapping in stroke induced aphasia. Hum Brain Mapp. 2021;42:5689–702. This connectivity study identifies a set of 10 short- and long-range parieto-temporal connections delineating the dorsal white matte circuitry of the dorsal language system.
pubmed: 34469044
pmcid: 8559486
doi: 10.1002/hbm.25647
Turken AU, Dronkers NF. The neural architecture of the language comprehension network: converging evidence from lesion and connectivity analyses. Front Syst Neurosci. 2011;5:1.
pubmed: 21347218
pmcid: 3039157
doi: 10.3389/fnsys.2011.00001
Friederici AD. White-Matter pathways for speech and language processing. Handb Clin Neurol. 2015;129:177–86.
pubmed: 25726269
doi: 10.1016/B978-0-444-62630-1.00010-X
Fridriksson J, den Ouden DB, Hillis AE, Hickok G, Rorden C, Basilakos A, Yourganov G, Bonilha L. Anatomy of aphasia revisited. Brain. 2018;141:848–62.
pubmed: 29360947
pmcid: 5837461
doi: 10.1093/brain/awx363
Zhang B, Chang J, Park J, Tan Z, Tang L, Lyu T, Han Y, Fan R, Gao Y, Kong J. Uncinate fasciculus and its cortical terminals in aphasia after subcortical stroke: a multi-modal MRI study. Neuroimage Clin. 2021;30:102597.
pubmed: 33684729
pmcid: 7941046
doi: 10.1016/j.nicl.2021.102597
Kim G, Jeong B, Choi M, Kim WS, Han CE, Paik NJ. Neural substrates of subcortical aphasia in subacute stroke: Voxel-based lesion symptom mapping study. J Neurol Sci. 2021;420:117266.
pubmed: 33341084
doi: 10.1016/j.jns.2020.117266
Radanovic M, Mansur LL. Aphasia in vascular lesions of the basal ganglia: a comprehensive review. Brain Lang. 2017;173:20–32.
pubmed: 28570947
doi: 10.1016/j.bandl.2017.05.003
Weiller C, Willmes K, Reiche W, Thron A, Isensee C, Buell U, Ringelstein EB. The case of aphasia or neglect after striatocapsular infarction. Brain. 1993;116:1509–25.
pubmed: 8293284
doi: 10.1093/brain/116.6.1509
Nadeau SE, Crosson B. Subcortical aphasia. Brain Lang. 1997;58:355–402. discussion 418 – 23.
pubmed: 9222518
doi: 10.1006/brln.1997.1707
Hillis AE, Wityk RJ, Barker PB, Beauchamp NJ, Gailloud P, Murphy K, Cooper O, Metter EJ. Subcortical aphasia and neglect in acute stroke: the role of cortical hypoperfusion. Brain. 2002;125:1094–104.
pubmed: 11960898
doi: 10.1093/brain/awf113
Hillis AE, Barker PB, Wityk RJ, Aldrich EM, Restrepo L, Breese EL, Work M. Variability in subcortical aphasia is due to variable sites of cortical hypoperfusion. Brain Lang. 2004;89:524–30.
pubmed: 15120543
doi: 10.1016/j.bandl.2004.01.007
Han MK, Kang DW, Jeong SW, Roh JK. Aphasia following striatocapsular infarction may be explained by concomitant small cortical infarct on diffusion-weighted imaging. Cerebrovasc Dis. 2005;19:220–4.
pubmed: 15703465
doi: 10.1159/000083886
Choi JY, Lee KH, Na DL, Byun HS, Lee SJ, Kim H, Kwon M, Lee KH, Kim BT. Subcortical aphasia after striatocapsular infarction: quantitative analysis of brain perfusion SPECT using statistical parametric mapping and a statistical probabilistic anatomic map. J Nucl Med. 2007;48:194–200.
pubmed: 17268014
Celebi U, Oztekin MF, Kucuk NO. Which is responsible for aphasia by subcortical lesions? Subcortical lesions or the cortical hypoperfusion? Neurol Res. 2022;44:1066–73.
pubmed: 35984244
doi: 10.1080/01616412.2022.2112369
Vallar G, Perani D, Cappa SF, Messa C, Lenzi GL, Fazio F. Recovery from aphasia and neglect after subcortical stroke: neuropsychological and cerebral perfusion study. J Neurol Neurosurg Psychiatry. 1988;51:1269–76.
pubmed: 2465386
pmcid: 1032915
doi: 10.1136/jnnp.51.10.1269
Radanovic M, Mansur LL, Azambuja MJ, Porto CS, Scaff M. Contribution to the evaluation of language disturbances in subcortical lesions: a pilot study. Arq Neuropsiquiatr. 2004;62:51–7.
pubmed: 15122433
doi: 10.1590/S0004-282X2004000100009
de Boissezon X, Démonet JF, Puel M, Marie N, Raboyeau G, Albucher JF, Chollet F, Cardebat D. Subcortical aphasia: a longitudinal PET study. Stroke. 2005;36:1467–73.
pubmed: 15933252
doi: 10.1161/01.STR.0000169947.08972.4f
Nakagawa T, Murata Y, Kojima T, Shinkai Y, Yamaya Y, Kato M, Shibuya H. Prognostic value of brain perfusion single-photon emission computed tomography (SPECT) for language recovery in patients with aphasia. Nucl Med Commun. 2005;26:919–23.
pubmed: 16160652
doi: 10.1097/00006231-200510000-00011
Munakomi S, Das JM, Neuroanatomy. Recurrent Artery of Heubner. [Updated 2023 Aug 28]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024. https://www.ncbi.nlm.nih.gov/books/NBK545222/
Carrera E, Tononi G. Diaschisis: past, present, future. Brain. 2014;137:2408–22.
pubmed: 24871646
doi: 10.1093/brain/awu101
Perani D, Vallar G, Cappa S, Messa C, Fazio F. Aphasia and neglect after subcortical stroke. A clinical/cerebral perfusion correlation study. Brain. 1987;110:1211–29.
pubmed: 3499949
doi: 10.1093/brain/110.5.1211
Demeurisse G, Capon A, Verhas M, Attig E. Pathogenesis of aphasia in deep-seated lesions: likely role of cortical diaschisis. Eur Neurol. 1990;30:67–74.
pubmed: 2340837
doi: 10.1159/000117313
Giroud M, Lemesle M, Madinier G, Billiar T, Dumas R. Unilateral lenticular infarcts: radiological and clinical syndromes, aetiology, and prognosis. J Neurol Neurosurg Psychiatry. 1997;63:611–5.
pubmed: 9408102
pmcid: 2169829
doi: 10.1136/jnnp.63.5.611
Radanovic M, Scaff M. Speech and language disturbances due to subcortical lesions. Brain Lang. 2003;84:337–52.
pubmed: 12662975
doi: 10.1016/S0093-934X(02)00554-0
El-Wahsh S, Greenup D, White G, Thompson EO, Aggarwal A, Fulham MJ, Halmagyi GM. Diaschisis: a mechanism for subcortical aphasia? J Neurol. 2022;269:2219–21. This is an interesting case study providing neuroimaging in a left putaminal hemorrhage.
pubmed: 34689219
doi: 10.1007/s00415-021-10861-7
Duering M, Righart R, Csanadi E, Jouvent E, Hervé D, Chabriat H, Dichgans M. Incident subcortical infarcts induce focal thinning in connected cortical regions. Neurology. 2012;79:2025–8.
pubmed: 23054230
doi: 10.1212/WNL.0b013e3182749f39
Duering M, Righart R, Wollenweber FA, Zietemann V, Gesierich B, Dichgans M. Acute infarcts cause focal thinning in remote cortex via degeneration of connecting fiber tracts. Neurology. 2015;84:1685–92.
pubmed: 25809303
pmcid: 4409580
doi: 10.1212/WNL.0000000000001502
Tang H, Fan S, Niu X, Li Z, Xiao P, Zeng J, Xing S. Remote cortical atrophy and language outcomes after chronic left subcortical stroke with aphasia. Front Neurosci. 2022;16:853169.
pubmed: 35992910
pmcid: 9381815
doi: 10.3389/fnins.2022.853169
Shine JM, Lewis LD, Garrett DD, Hwang K. The impact of the human thalamus on brain-wide information processing. Nat Rev Neurosci. 2023;24:416–30.
pubmed: 37237103
pmcid: 10970713
doi: 10.1038/s41583-023-00701-0
Fritsch M, Rangus I, Nolte CH. Thalamic aphasia: a review. Curr Neurol Neurosci Rep. 2022;22:855–65.
pubmed: 36383308
pmcid: 9750901
doi: 10.1007/s11910-022-01242-2
Radanovic M, Almeida VN. Subcortical aphasia. Curr Neurol Neurosci Rep. 2021;21:73.
pubmed: 34817710
doi: 10.1007/s11910-021-01156-5
Rangus I, Rios AS, Horn A, Fritsch M, Khalil A, Villringer K, Udke B, Ihrke M, Grittner U, Galinovic I, Al-Fatly B, Endres M, Kufner A, Nolte CH. Fronto-thalamic networks and the left ventral thalamic nuclei play a key role in aphasia after thalamic stroke. Commun Biol. 20247;7:700.
Sweeney-Reed CM, Buentjen L, Voges J, Schmitt FC, Zaehle T, Kam JWY, Kaufmann J, Heinze HJ, Hinrichs H, Knight RT, Rugg MD. The role of the anterior nuclei of the thalamus in human memory processing. Neurosci Biobehav Rev. 2021;126:146–58.
pubmed: 33737103
doi: 10.1016/j.neubiorev.2021.02.046
Geier KT, Buchsbaum BR, Parimoo S, Olsen RK. The role of anterior and medial dorsal thalamus in associative memory encoding and retrieval. Neuropsychologia. 2020;148:107623.
pubmed: 32918952
doi: 10.1016/j.neuropsychologia.2020.107623
Chomsung RD, Wei H, Day-Brown JD, Petry HM, Bickford ME. Synaptic organization of connections between the temporal cortex and pulvinar nucleus of the tree shrew. Cereb Cortex. 2010;20:997–1011.
pubmed: 19684245
doi: 10.1093/cercor/bhp162
Benarroch EE. Pulvinar: associative role in cortical function and clinical correlations. Neurology. 2015;84:738–47.
pubmed: 25609762
doi: 10.1212/WNL.0000000000001276
Liu J, Cui Z, Li L. Local and whole-network topologies reveal that pulvinar and semantic hub interactions correlate with picture vocabulary. NeuroReport. 2020;31:590–6.
pubmed: 32366811
doi: 10.1097/WNR.0000000000001444
Winiarski HR. The relationship between thalamic morphology and behavioral features in amnestic and aphasic variants of Alzheimer’s Disease (Doctoral dissertation, Brigham Young University).2022.
Rotshtein P, Soto D, Grecucci A, Geng JJ, Humphreys GW. The role of the pulvinar in resolving competition between memory and visual selection: a functional connectivity study. Neuropsychologia. 2011;49:1544–52.
pubmed: 21172363
doi: 10.1016/j.neuropsychologia.2010.12.002
Almeida VN. The neural hierarchy of consciousness: a theoretical model and review on neurophysiology and NCCs. Neuropsychologia. 2022;169:108202.
pubmed: 35271856
doi: 10.1016/j.neuropsychologia.2022.108202
Hwang K, Bruss J, Tranel D, Boes AD. Network Localization of Executive Function Deficits in patients with focal thalamic lesions. J Cogn Neurosci. 2020;32:2303–19.
pubmed: 32902335
pmcid: 7606569
doi: 10.1162/jocn_a_01628
Hills TT, Jones MN, Todd PM. Optimal foraging in semantic memory. Psychol Rev. 2012;119:431–40.
pubmed: 22329683
doi: 10.1037/a0027373
Hirshorn EA, Thompson-Schill SL. Role of the left inferior frontal gyrus in covert word retrieval: neural correlates of switching during verbal fluency. Neuropsychologia. 2006;44:2547–57.
pubmed: 16725162
doi: 10.1016/j.neuropsychologia.2006.03.035
Wright NF, Vann SD, Aggleton JP, Nelson AJ. A critical role for the anterior thalamus in directing attention to task-relevant stimuli. J Neurosci. 2015;35:5480–8.
pubmed: 25855166
pmcid: 4388916
doi: 10.1523/JNEUROSCI.4945-14.2015
Almeida VN. Neurophysiological basis of the N400 deflection, from Mismatch Negativity to Semantic Prediction potentials and late positive components. Int J Psychophysiol. 2021;166:134–50.
pubmed: 34097935
doi: 10.1016/j.ijpsycho.2021.06.001
León-Cabrera P, Hjortdal A, Berthelsen SG, Rodríguez-Fornells A, Roll M. Neurophysiological signatures of prediction in language: a critical review of anticipatory negativities. Neurosci Biobehav Rev. 2024;160:105624.
pubmed: 38492763
doi: 10.1016/j.neubiorev.2024.105624
Roll M, Söderström P, Horne M, Hjortdal A. Pre-activation negativity (PrAN): a neural index of predictive strength of phonological cues. Lab Phonol. 2023;14:1.
doi: 10.16995/labphon.6438
Javitt DC, Lee M, Kantrowitz JT, Martinez A. Mismatch negativity as a biomarker of theta band oscillatory dysfunction in schizophrenia. Schizophr Res. 2018;191:51–60.
pubmed: 28666633
doi: 10.1016/j.schres.2017.06.023
Lakatos P, O’Connell MN, Barczak A, McGinnis T, Neymotin S, Schroeder CE, Smiley JF, Javitt DC. The Thalamocortical Circuit of Auditory Mismatch Negativity. Biol Psychiatry. 2020;87(8):770–80.
pubmed: 31924325
doi: 10.1016/j.biopsych.2019.10.029
Jankowski MM, Ronnqvist KC, Tsanov M, Vann SD, Wright NF, Erichsen JT, Aggleton JP, O’Mara SM. The anterior thalamus provides a subcortical circuit supporting memory and spatial navigation. Front Syst Neurosci. 2013;7:45.
pubmed: 24009563
pmcid: 3757326
doi: 10.3389/fnsys.2013.00045
Zhou H, Schafer RJ, Desimone R. Pulvinar-cortex interactions in vision and attention. Neuron. 2016;89:209–20.
pubmed: 26748092
pmcid: 4723640
doi: 10.1016/j.neuron.2015.11.034
Basha D, Dostrovsky JO, Lopez Rios AL, Hodaie M, Lozano AM, Hutchison WD. Beta oscillatory neurons in the motor thalamus of movement disorder and pain patients. Exp Neurol. 2014;261:782–90.
pubmed: 25205228
doi: 10.1016/j.expneurol.2014.08.024
Basha D, Kalia SK, Hodaie M, Lopez Rios AL, Lozano AM, Hutchison WD. Beta band oscillations in the motor thalamus are modulated by visuomotor coordination in essential tremor patients. Front Hum Neurosci. 2023;17:1082196.
pubmed: 37180551
pmcid: 10169705
doi: 10.3389/fnhum.2023.1082196
Nadeau SE. Basal ganglia and thalamic contributions to Language function: insights from a parallel distributed Processing Perspective. Neuropsychol Rev. 2021;31:495–515. The author presents an interesting view of the role of these subcortical structures in language under the scope of the parallel distribution processing model, defending that the basal ganglia have a primarily computational function (reduction of a large amount of sensorimotor input to be automatically translated into optimal behavior); the thalamus, would subserve an role in integration of cortical input to permit a full concept representation.
pubmed: 33512608
doi: 10.1007/s11065-020-09466-0