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期刊名:Neurophysiologie clinique-clinical neurophysiology

缩写:NEUROPHYSIOL CLIN

ISSN:0987-7053

e-ISSN:1769-7131

IF/分区:2.4/Q2

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Oliver Bichsel,Stephen Bacchi,Mehdi Hajiabadi et al. Oliver Bichsel et al.
Objectives: Increased beta-oscillations (13-35 Hz) in the basal ganglia have been linked to Parkinsonian motor symptoms. Deep brain stimulation (DBS) approaches have been proposed to mitigate pathological beta-activity, w...
Alessandro Consales,Luca Bosisio,Domenico Tortora et al. Alessandro Consales et al.
Stereo-EEG is a fundamental part of the diagnostic process for a significant number of selected patients with focal epilepsy. The complexity inherent in planning a SEEG study means that this method can only reasonably be put into practice i...
José Luis Guerrero Solano,Oscar Ayo-Martin,Tomas Segura José Luis Guerrero Solano
This observational open-label study evaluates the clinical and neurophysiological effects of multiple sessions of contralesional motor cortex low-frequency repetitive transcranial magnetic stimulation (LF-rTMS) on seventeen patients with ch...
Katy Jerčinović,Katarina Tešija,Mašan Sredanović et al. Katy Jerčinović et al.
Objective: To characterize sweating issues in people with multiple sclerosis (pwMS) using the Quantitative Sudomotor Axon Reflex Test (QSART) and SUDOSCAN. ...
Ah-Hyeon Kim,Ga Yang Shim,Yunsoo Soh et al. Ah-Hyeon Kim et al.
Introduction: The House-Brackmann grading system exhibits inherent subjectivity despite widespread clinical adoption. Although electrophysiological assessments provide objective neurophysiological data, their correlation ...
Lina Jeantin,Louis Cousyn,Vincent Navarro et al. Lina Jeantin et al.
Sleep disturbances in anti-NMDAR encephalitis evolve dynamically across disease phases. We monitored a patient longitudinally from the acute phase through remission, relapse, and recovery, using video-EEG and polysomnography. No sleep compl...
Bade Güleç,Melda Acar,Yeşim Oruç et al. Bade Güleç et al.
Aims: Spinal muscular atrophy (SMA) is a genetic neuromuscular disorder characterized by progressive motor neuron degeneration, leading to symmetrical proximal weakness, bulbar dysfunction, and respiratory involvement. Al...