cTBS over contralesional homologue areas deteriorates speech output in isolated apraxia of speech after stroke

Kaufmann, Brigitte C.; Pastore-Wapp, Manuela; Lübeck, Maria; Koenig, Monica; Bohlhalter, Stephan; Vanbellingen, Tim; Cazzoli, Dario; Nyffeler, Thomas (2019). cTBS over contralesional homologue areas deteriorates speech output in isolated apraxia of speech after stroke. Brain stimulation, 12(4), pp. 1069-1071. Elsevier 10.1016/j.brs.2019.03.024

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Apraxia of speech (AOS) is an impairment of motor speech planning/programming, characterized by a combination of phonemic segmental changes and articulatory distortions [1]. AOS is most often accompanied by aphasia, whereas isolated forms may rarely occur after focal damage to the left precentral gyrus [1]. How AOS recovers after brain damage is poorly understood [2]. In particular, it is not known whether recovery of AOS solely depends on the functional reorganisation of perilesional areas [3,4], or whether it also depends on the compensation through contralesional homologue areas.

Item Type:

Journal Article (Further Contribution)

Division/Institute:

04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Neurology
04 Faculty of Medicine > Department of Radiology, Neuroradiology and Nuclear Medicine (DRNN) > Institute of Diagnostic and Interventional Neuroradiology
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DCR Unit Sahli Building > Forschungsgruppe Neurologie
10 Strategic Research Centers > ARTORG Center for Biomedical Engineering Research > ARTORG Center - Gerontechnology and Rehabilitation

Graduate School:

Graduate School for Health Sciences (GHS)

UniBE Contributor:

Pastore-Wapp, Manuela, Bohlhalter, Stephan, Vanbellingen, Tim, Cazzoli, Dario, Nyffeler, Thomas

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1935-861X

Publisher:

Elsevier

Language:

English

Submitter:

Angela Amira Botros

Date Deposited:

30 Jul 2019 17:01

Last Modified:

05 Dec 2022 15:28

Publisher DOI:

10.1016/j.brs.2019.03.024

PubMed ID:

30914261

BORIS DOI:

10.7892/boris.130363

URI:

https://boris.unibe.ch/id/eprint/130363

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