scholarly journals miR-139-5p modulates cortical neuronal migration by targeting Lis1 in a rat model of focal cortical dysplasia

2014 ◽  
Vol 33 (6) ◽  
pp. 1407-1414 ◽  
Author(s):  
YANJUN HUANG ◽  
JIAO JIANG ◽  
GUO ZHENG ◽  
JING CHEN ◽  
HAIYING LU ◽  
...  
Author(s):  
Abhay Deshmukh ◽  
Jared Leichner ◽  
Jihye Bae ◽  
Yinchen Song ◽  
Pedro A. Valdés-Hernández ◽  
...  

Brain ◽  
2011 ◽  
Vol 134 (10) ◽  
pp. 2828-2843 ◽  
Author(s):  
Francesca Colciaghi ◽  
Adele Finardi ◽  
Angelisa Frasca ◽  
Silvia Balosso ◽  
Paola Nobili ◽  
...  

2004 ◽  
Vol 19 (3) ◽  
pp. 357-363
Author(s):  
Hiroshi Otsubo ◽  
Koji Iida ◽  
Makoto Oishi ◽  
Chiyuki Okuda ◽  
Ayako Ochi ◽  
...  

We define specific neurophysiologic characteristics for focal cortical dysplasia, a neuronal migration disorder. We reviewed data from published reports and our patients with focal cortical dysplasia. Our patients underwent preoperative scalp video-electroencephalography (EEG), magnetic resonance imaging (MRI), magnetoencephalography, and intraoperative or extraoperative electrocorticography monitoring. Scalp EEG showed trains of rhythmic epileptiform spike or sharp waves. Positive spikes correlated with early seizure onset, MRI lesion around the rolandic fissure, hemiparesis, and a less favorable outcome. Interictal electrocorticography showed continuous epileptogenic discharges: repetitive electrographic seizures and bursting discharges or continuous or quasicontinuous rhythmic spiking. Ictal electrocorticography showed paroxysmal fast and/or repetitive spiking. Magnetoencephalography showed clustered spike sources within and extending from the lesion. Cortical stimulation gave more frequent, lower-threshold afterdischarges and higher-threshold primary motor function. Focal cortical dysplasias are highly and intrinsically epileptogenic. For surgical seizure control, EEG, electrocorticography, and magnetoencephalography must delineate the intrinsic epileptogenic zone within and extending from the focal cortical dysplasia identified by MRI. ( J Child Neurol 2005;20:357—363).


Author(s):  
André Palmini ◽  
Frederick Andermann ◽  
André Olivier ◽  
Donatella Tampieri ◽  
Yvon Robitaille ◽  
...  

ABSTRACT:Computed tomography and magnetic resonance imaging enable the identification of neuronal migration disorders during life. Several specific syndromes have been identified and early diagnosis of previously unrecognized entities is now possible. We report 51 patients with imaging. Thirty-two had a single widespread cortical dysplastic lesion. Twenty-eight had focal corticectomies. From a pathological standpoint, these encompassed focal cortical dysplasia (14 cases) and forme fruste of tuberous sclerosis (10 cases). These two groups of patients were indistinguishable from the clinical and radiological standpoint. In only two was the MRI examination normal. In addition, there were 10 with bilateral perisylvian dysplasia, four with diffuse cortical dysplasia or the "double cortex" syndrome, three with hemimegalencephaly, one with megalencephaly, and one with nodular neuronal heterotopia. The electroclinical and imaging findings led to the development of specific surgical strategies for the alleviation of the intractable seizures in each of these radiologically-defined syndromes.


Epilepsia ◽  
2021 ◽  
Author(s):  
Hsin‐Yi Kao ◽  
Shuntong Hu ◽  
Temenuzhka Mihaylova ◽  
Julie Ziobro ◽  
EunSeon Ahn ◽  
...  

2001 ◽  
Vol 42 (12) ◽  
pp. 839 ◽  
Author(s):  
Kenjiro Gondo ◽  
Ryutaro Kira ◽  
Yoichi Tokunaga ◽  
Chie Harashima ◽  
Shozo Tobimatsu ◽  
...  

2019 ◽  
Vol 24 (3) ◽  
pp. 284-292
Author(s):  
Eisha A. Christian ◽  
Elysa Widjaja ◽  
Ayako Ochi ◽  
Hiroshi Otsubo ◽  
Stephanie Holowka ◽  
...  

OBJECTIVESmall lesions at the depth of the sulcus, such as with bottom-of-sulcus focal cortical dysplasia, are not visible from the surface of the brain and can therefore be technically challenging to resect. In this technical note, the authors describe their method of using depth electrodes as landmarks for the subsequent resection of these exacting lesions.METHODSA retrospective review was performed on pediatric patients who had undergone invasive electroencephalography with depth electrodes that were subsequently used as guides for resection in the period between July 2015 and June 2017.RESULTSTen patients (3–15 years old) met the criteria for this study. At the same time as invasive subdural grid and/or strip insertion, between 2 and 4 depth electrodes were placed using a hand-held frameless neuronavigation technique. Of the total 28 depth electrodes inserted, all were found within the targeted locations on postoperative imaging. There was 1 patient in whom an asymptomatic subarachnoid hemorrhage was demonstrated on postprocedural imaging. Depth electrodes aided in target identification in all 10 cases.CONCLUSIONSDepth electrodes placed at the time of invasive intracranial electrode implantation can be used to help localize, target, and resect primary zones of epileptogenesis caused by bottom-of-sulcus lesions.


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