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Matteo Bologna

Researcher at Sapienza University of Rome

Publications -  143
Citations -  3284

Matteo Bologna is an academic researcher from Sapienza University of Rome. The author has contributed to research in topics: Transcranial magnetic stimulation & Medicine. The author has an hindex of 30, co-authored 117 publications receiving 2379 citations. Previous affiliations of Matteo Bologna include UCL Institute of Neurology & University College London.

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Correlation between cortical plasticity, motor learning and BDNF genotype in healthy subjects.

TL;DR: The present results emphasise that although some TMS measures of cortical plasticity may correlate with each other, they may not always relate directly to measures of behavioural learning.
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Functional reorganization of sensorimotor cortex in early Parkinson disease

TL;DR: Increased motor cortical plasticity on the less affected side is consistent with a functional reorganization of sensorimotor cortex and may represent a compensatory change that contributes to delaying onset of clinical symptoms.
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Voluntary, spontaneous, and reflex blinking in Parkinson's disease.

TL;DR: In PD patients the longer pauses between the closing and opening phase in comparison to normal subjects, suggest bradykinesia of voluntary blinking and PD patients also display kinematic abnormalities of spontaneous blinking and changes in the excitability of the closing phase of reflex blinking.
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Evolving concepts on bradykinesia.

TL;DR: Clinical and experimental studies on bradykinesia performed in patients with Parkinson's disease and atypical parkinsonism are reviewed and the role of the basal ganglia and other interconnected structures, such as the primary motor cortex and cerebellum, as well as the contribution of abnormal sensorimotor processing are demonstrated.
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A comparative study of primary and secondary hemifacial spasm

TL;DR: Patients with primary and those with secondary HFS share common demographic and clinical features, including sex distribution, age at onset, affected side of HFS, synkinesis, and rarity of familial cases.