Raffaele  Nardone

Prof. Raffaele Nardone

Hospital Merano SABES ASDAA, Department of Neurology, Via Rossini 5, I-39012 Merano Meran, Italy
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Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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6 April 2005 in The Journal of Physiology
Verified
Journal Article
Open access
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VLVincenzo Di Lazzaro
Vincenzo Di Lazzaro
AOA. Oliviero
A. Oliviero
ESE. Saturno
E. Saturno
MDM. Dileone
M. Dileone
FPfabio pilato
fabio pilato
PTP. Tonali
P. Tonali
Experimental studies have demonstrated that the GABAergic system modulates acetylcholine release and, through GABAA receptors, tonically inhibits cholinergic activity. Little is known about the effects of GABA on the cholinergic activity in the human central nervous system. In vivo evaluation of some cholinergic circuits of the human brain has recently been introduced using a transcranial magnetic stimulation (TMS) protocol based on coupling peripheral nerve stimulation with TMS of the motor cortex. Peripheral nerve inputs have an inhibitory effect on motor cortex excitability at short intervals (short latency afferent inhibition, SAI). We investigated whether GABAA activity enhancement by lorazepam modifies SAI. We also evaluated the effects produced by lorazepam on a different TMS protocol of cortical inhibition, the short interval intracortical inhibition (SICI), which is believed to be directly related to GABAA activity. In 10 healthy volunteers, the effects of lorazepam were compared with those produced by quetiapine, a psychotropic drug with sedative effects with no appreciable affinity at cholinergic muscarinic and benzodiazepine receptors, and with those of a placebo using a randomized double‐blind study design. Administration of lorazepam produced a significant increase in SICI (F3,9= 3.19, P= 0.039). In contrast to SICI, SAI was significantly reduced by lorazepam (F3,9= 9.39, P= 0.0002). Our findings demonstrate that GABAA activity enhancement determines a suppression of SAI and an increase of SICI.

1 January 2016 in Journal of Clinical Neurology
Verified
Journal Article
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Raffaele  NardoneRaffaele Nardone
Raffaele Nardone
Francesco BrigoFrancesco Brigo
Francesco Brigo
ETEugen Trinka
Eugen Trinka
Nardone R, et al. J Clin Neurol. 2016 Jan;12(1):21-33. https://doi.org/10.3988/jcn.2016.12.1.21

1 April 2013 in Brain Research
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Journal Article
Closed access
Raffaele  NardoneRaffaele Nardone
Raffaele Nardone
Yvonne HöllerYvonne Höller
Yvonne Höller
Francesco BrigoFrancesco Brigo
Francesco Brigo
MSMartin Seidl
Martin Seidl
MCMonica Christova
Monica Christova
ETEugen Trinka
Eugen Trinka

20 October 2015 in Frontiers in Human Neuroscience
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Yvonne HöllerYvonne Höller
Yvonne Höller
RKRaoul Kutil
Raoul Kutil
LKLukas Klaffenböck
Lukas Klaffenböck
ATAljoscha Thomschewski
Aljoscha Thomschewski
PHPeter M. Höller
Peter M. Höller
ETEugen Trinka
Eugen Trinka
High frequency oscillations (HFOs) are estimated as a potential marker for epileptogenicity. Current research strives for valid evidence that these HFOs could aid the delineation of the to-be resected area in patients with refractory epilepsy and improve surgical outcomes. In the present meta-analysis, we evaluated the relation between resection of regions from which HFOs can be detected and outcome after epilepsy surgery. We conducted a systematic review of all studies that related the resection of HFO-generating areas to postsurgical outcome. We related the outcome (seizure freedom) to resection ratio, that is, the ratio between the number of channels on which HFOs were detected and, among these, the number of channels that were inside the resected area. We compared the resection ratio between seizure free and not seizure free patients. In total, 11 studies were included. In 10 studies, ripples (80–200 Hz) were analyzed, and in 7 studies, fast ripples (>200 Hz) were studied. We found comparable differences (dif) and largely overlapping confidence intervals (CI) in resection ratios between outcome groups for ripples (dif = 0.18; CI: 0.10–0.27) and fast ripples (dif = 0.17; CI: 0.01–0.33). Subgroup analysis showed that automated detection (dif = 0.22; CI: 0.03–0.41) was comparable to visual detection (dif = 0.17; CI: 0.08–0.27). Considering frequency of HFOs (dif = 0.24; CI: 0.09–0.38) was related more strongly to outcome than considering each electrode that was showing HFOs (dif = 0.15; CI = 0.03–0.27). The effect sizes found in the meta-analysis are small but significant. Automated detection and application of a detection threshold in order to detect channels with a frequent occurrence of HFOs is important to yield a marker that could be useful in presurgical evaluation. In order to compare studies with different methodological approaches, detailed and standardized reporting is warranted.

8 February 2014 in Acta Neurologica Scandinavica
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Journal Article
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Raffaele  NardoneRaffaele Nardone
Raffaele Nardone
FTF. Tezzon
F. Tezzon
Yvonne HöllerYvonne Höller
Yvonne Höller
SGS. Golaszewski
S. Golaszewski
ETE. Trinka
E. Trinka
Francesco BrigoFrancesco Brigo
Francesco Brigo
Several Transcranial Magnetic Stimulation (TMS) techniques can be applied to noninvasively measure cortical excitability and brain plasticity in humans. TMS has been used to assess neuroplastic changes in Alzheimer's disease (AD), corroborating findings that cortical physiology is altered in AD due to the underlying neurodegenerative process. In fact, many TMS studies have provided physiological evidence of abnormalities in cortical excitability, connectivity, and plasticity in patients with AD. Moreover, the combination of TMS with other neurophysiological techniques, such as high‐density electroencephalography (EEG), makes it possible to study local and network cortical plasticity directly. Interestingly, several TMS studies revealed abnormalities in patients with early AD and even with mild cognitive impairment (MCI), thus enabling early identification of subjects in whom the cholinergic degeneration has occurred. Furthermore, TMS can influence brain function if delivered repetitively; repetitive TMS (rTMS) is capable of modulating cortical excitability and inducing long‐lasting neuroplastic changes. Preliminary findings have suggested that rTMS can enhance performances on several cognitive functions impaired in AD and MCI. However, further well‐controlled studies with appropriate methodology in larger patient cohorts are needed to replicate and extend the initial findings. The purpose of this paper was to provide an updated and comprehensive systematic review of the studies that have employed TMS/rTMS in patients with MCI and AD.

1 July 2020 in Sleep Medicine
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Journal Article
Closed access
Raffaele  NardoneRaffaele Nardone
Raffaele Nardone
LSLuca Sebastianelli
Luca Sebastianelli
VVViviana Versace
Viviana Versace
Francesco BrigoFrancesco Brigo
Francesco Brigo
SGStefan Golaszewski
Stefan Golaszewski
ETEugen Trinka
Eugen Trinka