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Dive into the research topics where Jean-Pierre Vignal is active.

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Featured researches published by Jean-Pierre Vignal.


Electroencephalography and Clinical Neurophysiology | 1995

Intracerebral potentials to rare target and distractor auditory and visual stimuli. II. Medial, lateral and posterior temporal lobe.

Eric Halgren; Patrick Baudena; Jeffrey M. Clarke; Gary Heit; Ksenija Marinkovic; Bertrand Devaux; Jean-Pierre Vignal; Arnauld Biraben

Event-related potentials were recorded from 1221 sites in the medial, lateral and posterior aspects of the temporal lobe in 39 patients. Depth electrodes were implanted for about 4 days in order to localize seizure origin prior to surgical treatment. Subjects received an auditory discrimination task with target and non-target rare stimuli. In some cases, the target, distracting and frequent tones were completely balanced across blocks for pitch and volume. Some subjects also received an analogous visual discrimination task, or auditory tasks in which the rare target event was the omission of a tone, or the repetition of a tone within a series of alternating tones. In some subjects, the same auditory stimuli were delivered but the patient ignored them while reading. A complex field was recorded, indicating multiple components with overlapping time-courses, task correlates and generators. Two general patterns could be distinguished on the basis of their waveforms, latencies and task correlates. In the temporal pole and some middle temporal, posterior parahippocampal and fusiform gyrus sites, a sharp triphasic negative-positive-negative waveform with peaks at about 220-320-420 msec was usually observed. This wave was of relatively small amplitude and diffuse, and seldom inverted in polarity. It was multimodal but most prominent to auditory stimuli, appeared to remain when the stimuli were ignored, and was not apparent to repeated words and faces. A second broad, often monophasic, waveform peaking at about 380 msec was generated in the hippocampus, a limited region of the superior temporal sulcus, and (by inference) in the anterobasal temporal lobe (possible rhinal cortex). This waveform was of large amplitude, often highly focal, and could invert over short distances. It was equal to visual and auditory stimuli, was greatly diminished when the stimuli were ignored, and was also evoked by repeating words and faces. Preceding this waveform was a non-modality-specific negativity, possibly generated in rhinal cortex, and a visual-specific negativity in inferotemporal cortex. The early triphasic pattern may embody a diffuse non-specific orienting response that is also reflected in the scalp P3a. The late monophasic pattern may embody the cognitive closure that is also reflected in the scalp P3b or late positive component.


Epilepsia | 2004

Semiologic and electrophysiologic correlations in temporal lobe seizure subtypes

Louis Maillard; Jean-Pierre Vignal; Martine Gavaret; Maxime Guye; Arnaud Biraben; Aileen McGonigal; Patrick Chauvel; Fabrice Bartolomei

Summary:  Purpose: The International League Against Epilepsy (ILAE) classification distinguishes medial and neocortical temporal lobe epilepsies. Among other criteria, this classification relies on the identification of two different electroclinical patterns, those of medial (limbic) and lateral (neocortical) temporal lobe seizures, depending on the structure initially involved in the seizure activity. Recent electrophysiologic studies have now identified seizures in which medial and neocortical structures are both involved at seizure onset. The purpose of the study was therefore to study the correlations of ictal semiology with the spatiotemporal pattern of discharge in temporal lobe seizures.


Epilepsy Research | 1996

The serotonergic innervation of the cerebral cortex in man and its changes in focal cortical dysplasia

Suzanne Trottier; Bertrand Evrard; Jean-Pierre Vignal; Jean-Marie Scarabin; Patrick Chauvel

We present the morphology and the laminar distribution of the serotonin (5-hydroxytryptamine, 5-HT) innervation of the cerebral cortex of patients who underwent cortical resection for partial seizures. The limits of the resections were established by stereoelectroencephalography. The 5-HT innervation was mapped by using an antiserum anti-5-HT. Two patients had cryptogenic epilepsies and two others had seizures related to focal cortical dysplasia. 5-HT immunoreactive axons were morphologically heterogeneous and projected diffusely to the cerebral cortex with regional-specific densities. Two types of terminal axon were demonstrated. Type I had large and spherical (intensely immunoreactive) varicosities and was distributed sparsely with a characteristic predominance in the molecular layer. Type II had fine and pleiomorphic varicosities (granular or fusiform) and was distributed through all cortical layers. The distribution of the 5-HT innervation varied according to the different architectonic areas investigated. The granular cortical areas characterized by a highly developed layer IV (primary somatosensory, primary visual and prefrontal cortices) had the highest density of 5-HT-ir fibers distributed from layer I to layer V. The agranular primary motor cortex had the lowest density with fibers preferentially seen in layers I, IIIa and V-VI. The orbital cortex with a poorly defined layer IV had an intermediate density with a laminar repartition predominant in the supragranular layers. In patients with cryptogenic epilepsies, the brain epileptogenic tissue was histologically normal as well as the serotonergic innervation. In contrast, in patients with focal cortical dysplasia, the dysplastic epileptogenic tissue was characterized by a serotonergic hyperinnervation. In agreement with previous data in primates, we give morphological evidence for two morphologically distinct serotonergic subsystems and for regional specific densities in the human cerebral cortex. Moreover, we previously reported an altered pattern of the catecholaminergic innervation in the same dysplasia areas. All these results provide evidence that this development epileptogenic lesion involves several sets of neurons which may contribute to epileptogenic activity.


Epilepsia | 2006

Remote Memory in Temporal Lobe Epilepsy

Virginie Voltzenlogel; Olivier Després; Jean-Pierre Vignal; Bernhard J. Steinhoff; Pierre Kehrli; Lilianne Manning

Summary:  Purpose: The present study aims at characterizing remote memory in patients with temporal lobe epilepsy (TLE); it also considers the impact of its most important variables (lateralization of the lesion, duration of epilepsy, age at onset, and seizure frequency) on remote memory.


Epilepsia | 1998

Correlation Between Interictal Regional Cerebral Blood Flow and Depth-Recorded Interictal Spiking in Temporal Lobe Epilepsy

Benoit Guillon; Roderick Duncan; Arnaud Biraben; Anne-Marie Bernard; Jean-Pierre Vignal; Patrick Chauvel

Summary: Purpose: Single photon emission computed tomography (SPECT) is used as an adjunctive method in preoperative localization of epileptic foci. In temporal lobe epilepsy (TLE), interictal hypoperfusion is observed in 60–70% of cases. Correlation with ictal EEG changes is observed in ∼50–60% of cases. Relationships with interictal EEG have been studied less. We compared interictal SPECT data obtained in 20 patients with their interictal intracerebral electrical activity recorded by depth electrodes to evaluate a potential relationship.


Cognitive Neuropsychology | 2000

Localised face processing by the human prefrontal cortex : Stimulation-evoked hallucinations of faces

Jean-Pierre Vignal; Patrick Chauvel; Eric Halgren

Left and right prefrontal, premotor, and anterior temporal sites were stereotaxically implanted in order to direct surgical therapy for epilepsy. Direct electrical stimulation of the right anterior inferior frontal gyrus resulted in face-related hallucinations and illusions. When the patient was viewing a blank background, stimulation induced the experience of a rapid succession of faces. When the patient was viewing a real face, stimulation induced a series of modifications to that face. Effective stimulations induced afterdischarges that remained localised to right ventrolateral prefrontal cortex (VLPFC). Stimulation of other frontal and anterior temporal sites, bilaterally, induced no face-related hallucinations or illusions. This result supports a contribution of right VLPFC to face processing, and is consistent with models wherein it activates representations in working or declarative memories.


Epilepsia | 1997

Ictal Single Photon Emission Computed Tomography in Occipital Lobe Seizures

Roderick Duncan; Amaud Biraben; James Patterson; Donald M. Hadley; Anne-Marie Bernard; Joseph Lecloirec; Jean-Pierre Vignal; Patrick Chauvel

Summary: Purpose: Ictal single photon emission computed tomography (SPECT) has been evaluated as an adjunctive localizing technique in temporal lobe epilepsies and, to a lesser degree, in some extratemporal epilepsies. The purpose of this study was to determine whether occipital lobe seizures are associated with distinctive ictal cerebral blood perfusion (rCP) patterns.


Clinical Neurophysiology | 2009

Combined SEEG and source localisation study of temporal lobe schizencephaly and polymicrogyria.

Louis Maillard; Laurent Koessler; Sophie Colnat-Coulbois; Jean-Pierre Vignal; Valérie Louis-Dorr; Pierre-Yves Marie; Hervé Vespignani

OBJECTIVES Type 1 schizencephaly (SZ) is a cerebral malformation characterised by a cleft lined and surrounded by a polymicrogyric cortex, extending from the pial region to the peri-ventricular heterotopia. Our purpose was to combine and compare dipole source imaging technique and Stereo-EEG (SEEG) technique in determining the irritative and epileptogenic zones in a case of type 1 schizencephaly. METHODS High-resolution (64-channel) video-EEG with electrical source imaging and SEEG recordings were performed during a pre-surgical evaluation for medically intractable epilepsy. RESULTS Anatomo-electro-clinical correlations based on SEEG and source localisation identified two irritative and epileptogenic zones partially overlapping the polymicrogyric cortex surrounding the SZ: an anterior medio-lateral network primarily involving dysplasic limbic structures and a lateral network involving the anterior and middle part of the cleft and polymicrogyric cortex. The most posterior part (at the temporo-parieto-occipital junction) displayed a normal background activity. CONCLUSIONS Both epileptogenic and electrophysiologically normal cortices coexisted within the same widespread malformation: only the anterior part belonged to the anterior medio-lateral epileptogenic network defined by the SEEG. SIGNIFICANCE In cases of widespread cortical malformation such as SZ, source localization techniques can help to define the irritative zone and relevant targets for SEEG.


Epilepsia | 2002

Neural Networks Underlying Epileptic Humming

Fabrice Bartolomei; Fabrice Wendling; Jean-Pierre Vignal; Patrick Chauvel; Catherine Liégeois-Chauvel

Summary:  Purpose: Humming is a rare automatism occurring in partial seizures that has received little attention. Its study could shed light on the neural networks underlying melodic expression. In this study, we examined the anatomoelectroclinical correlates of humming during epileptic seizures


NeuroImage | 2008

Automatic localization and labeling of EEG sensors (ALLES) in MRI volume

Laurent Koessler; Adnane Benhadid; Louis Maillard; Jean-Pierre Vignal; Jacques Felblinger; Hervé Vespignani; Marc Braun

Spatial localization of scalp EEG electrodes is a major step for dipole source localization and must be accurate, reproducible and practical. Several methods have been proposed in the last 15 years. The most widely used method is currently electromagnetic digitization. Nevertheless, this method is difficult to use in a clinical environment and has not been validated with a high number of electrodes. In this paper, we introduce a new automatic method for localizing and labeling EEG sensors using MRI. First, we design a new scalp EEG sensor. Secondly, we validate this new technique on a head phantom and then in a clinical environment with volunteers and patients. For this, we compare the reproducibility, accuracy and performance of our method with electromagnetic digitization. We demonstrate that our method provides better reproducibility with a significant difference (p<0.01). Concerning precision, both methods are equally accurate with no statistical differences. To conclude, our method offers the possibility of using MRI volume for both source localization and spatial localization of EEG sensors. Automation makes this method very reproducible and easy to handle in a routine clinical environment.

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Sophie Colnat-Coulbois

Centre national de la recherche scientifique

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Edouard Hirsch

University of Strasbourg

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Francine Chassoux

Paris Descartes University

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