Find information on thousands of medical conditions and prescription drugs.

Cortical dysplasia

Cortical dysplasia is a benign tumor which occurs when the infant brain is developing in the womb. Occasionally neurons will develop that are larger than normal in certain areas. This causes the signals sent through the neurons in these areas to misfire, which sends an incorrect signal. It is commonly found near the cerebral cortex and is associated with seizures and often some level of mental retardation. Instead of using medication to suppress the seizures, surgery is increasingly becoming a popular solution for the problem.

Home
Diseases
A
B
C
Angioedema
C syndrome
Cacophobia
Café au lait spot
Calcinosis cutis
Calculi
Campylobacter
Canavan leukodystrophy
Cancer
Candidiasis
Canga's bead symptom
Canine distemper
Carcinoid syndrome
Carcinoma, squamous cell
Carcinophobia
Cardiac arrest
Cardiofaciocutaneous...
Cardiomyopathy
Cardiophobia
Cardiospasm
Carnitine transporter...
Carnitine-acylcarnitine...
Caroli disease
Carotenemia
Carpal tunnel syndrome
Carpenter syndrome
Cartilage-hair hypoplasia
Castleman's disease
Cat-scratch disease
CATCH 22 syndrome
Causalgia
Cayler syndrome
CCHS
CDG syndrome
CDG syndrome type 1A
Celiac sprue
Cenani Lenz syndactylism
Ceramidase deficiency
Cerebellar ataxia
Cerebellar hypoplasia
Cerebral amyloid angiopathy
Cerebral aneurysm
Cerebral cavernous...
Cerebral gigantism
Cerebral palsy
Cerebral thrombosis
Ceroid lipofuscinois,...
Cervical cancer
Chagas disease
Chalazion
Chancroid
Charcot disease
Charcot-Marie-Tooth disease
CHARGE Association
Chediak-Higashi syndrome
Chemodectoma
Cherubism
Chickenpox
Chikungunya
Childhood disintegrative...
Chionophobia
Chlamydia
Chlamydia trachomatis
Cholangiocarcinoma
Cholecystitis
Cholelithiasis
Cholera
Cholestasis
Cholesterol pneumonia
Chondrocalcinosis
Chondrodystrophy
Chondromalacia
Chondrosarcoma
Chorea (disease)
Chorea acanthocytosis
Choriocarcinoma
Chorioretinitis
Choroid plexus cyst
Christmas disease
Chromhidrosis
Chromophobia
Chromosome 15q, partial...
Chromosome 15q, trisomy
Chromosome 22,...
Chronic fatigue immune...
Chronic fatigue syndrome
Chronic granulomatous...
Chronic lymphocytic leukemia
Chronic myelogenous leukemia
Chronic obstructive...
Chronic renal failure
Churg-Strauss syndrome
Ciguatera fish poisoning
Cinchonism
Citrullinemia
Cleft lip
Cleft palate
Climacophobia
Clinophobia
Cloacal exstrophy
Clubfoot
Cluster headache
Coccidioidomycosis
Cockayne's syndrome
Coffin-Lowry syndrome
Colitis
Color blindness
Colorado tick fever
Combined hyperlipidemia,...
Common cold
Common variable...
Compartment syndrome
Conductive hearing loss
Condyloma
Condyloma acuminatum
Cone dystrophy
Congenital adrenal...
Congenital afibrinogenemia
Congenital diaphragmatic...
Congenital erythropoietic...
Congenital facial diplegia
Congenital hypothyroidism
Congenital ichthyosis
Congenital syphilis
Congenital toxoplasmosis
Congestive heart disease
Conjunctivitis
Conn's syndrome
Constitutional growth delay
Conversion disorder
Coprophobia
Coproporhyria
Cor pulmonale
Cor triatriatum
Cornelia de Lange syndrome
Coronary heart disease
Cortical dysplasia
Corticobasal degeneration
Costello syndrome
Costochondritis
Cowpox
Craniodiaphyseal dysplasia
Craniofacial dysostosis
Craniostenosis
Craniosynostosis
CREST syndrome
Cretinism
Creutzfeldt-Jakob disease
Cri du chat
Cri du chat
Crohn's disease
Croup
Crouzon syndrome
Crouzonodermoskeletal...
Crow-Fukase syndrome
Cryoglobulinemia
Cryophobia
Cryptococcosis
Crystallophobia
Cushing's syndrome
Cutaneous larva migrans
Cutis verticis gyrata
Cyclic neutropenia
Cyclic vomiting syndrome
Cystic fibrosis
Cystinosis
Cystinuria
Cytomegalovirus
Dilated cardiomyopathy
Hypertrophic cardiomyopathy
Restrictive cardiomyopathy
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Medicines

Read more at Wikipedia.org


[List your site here Free!]


Localization of ictal and interictal bursting epileptogenic activity in focal cortical dysplasia: Agreement of magnetoencephalography and electrocorticography
From Neurological Research, 9/1/02 by Ishibashi, Hideaki

Focal cortical dysplasia (FCD) is often associated with severe partial epilepsy. In such cases, interictal frequent rhythmic bursting epileptiform activity (FBREA) on both scalp electroencephalography (EEG) and electrocorticography (ECoG) is generally accepted to be identical to the ictal epileptiform activity. We used magnetoencephalography (or Magnetic Source Imaging (MSI)) to determine the epileptogenic zone in a 6-year-old patient with histopathologically proven FCD and normal magnetic resonance imaging (MRI). MSI was used to localize the sources of both ictal activity and FRBEA, which was then compared with ECoG findings. The intracranial sources of both types of activity co-localized in the left inferior frontal and superior temporal gyri. The location and extent of the epileptogenic area determined by MSI was essentially identical to that determined directly through extra-operative ECoG. In the absence of structural abnormalities detectable on MRI, the noninvasive method of MSI provided valuable information regarding the location and extent of the primary epileptogenic area. This was critical for pre-surgical planning regarding placement of intracranial electrodes and for risk-benefit evaluation. [Neurol Res 2002; 24: 525-530]

Keywords: Focal cortical dysplasia; magnetoencephalography; electrocorticography; epileptogenicity; epilepsy surgery

INTRODUCTION

Several investigators have reported on the electrophysiological manifestations of focal cortical dysplasia (FCD)1-9. A common electrophysiological correlate of FCD consists of frequent rhythmic bursting epileptiform activity (FRBEA) that is more prominent on invasive electrocorticography (ECoG) than on the surface EEG interictally3,10 Given that FCD is often associated with very subtle structural abnormalities not detectable on MRI, pre-surgical planning relies on the localization of paroxysmal activity preceding seizures on ECoG recorded from chronically implanted electrodes. Although there are indications that FRBEA originates from the same region as ictal discharges, studies on the morphology and intracranial origin of the former by magnetoencephalography (MEG, otherwise known as Magnetic Source Imaging (MSI)) are rare. Establishing the relative utility of interictal FRBEA and ictal paroxysmal discharges is an important step if MEG is to be used for the pre-surgical localization of the primary epileptogenic zone in FCD4-6,11,12. The accuracy of MSI in the localization of neuronal populations that show briefly elevated levels of activity, such as those producing epileptiform discharges, can be very high (i.e., in the order of 2-3 mm)13. MSI evaluations typically rely only on interictal activity.

The present study provided the opportunity, firstly to examine the utility of interictal bursting activity, observed in both MEG and ECoG, for identifying the epileptogenic zone in FCD, and secondly, to assess the localization accuracy of MSI, by comparing the MEG-- based source locations of ictal and interictal discharges, with the localization of corresponding events obtained directly through extraoperative ECoG.

PROCEDURES

Case description

The patient was a 6-year-old, right-handed girl who was born full term. She had no perinatal problems and showed normal development up to the age of 2 years, when she was referred to a neurologist because of repeated complex partial seizures, lasting for 10-15 sec. The clinical semiology consisted of staring episodes with alteration in her levels of consciousness and right-sided facial twitching. Her seizures were initially infrequent, but over the last three months had increased dramatically. She typically had 5-10 per day, and occasionally up to 40 per day, even with aggressive medical treatment. In light of her refractory seizure disorder, she underwent a pre-surgical evaluation. Neurological examination was normal with the exception of mild bilateral facial weakness and a prominent oral motor apraxia.

An MRI was entirely normal and did not reveal any of the abnormalities often present in FCD, such as regional signal intensity changes, pachygyria or microgyria on T1 - and T2-weighted scans, or on fluid attenuated inversion recovery (FLAIR) images.

MEG recording

MEG recording was performed pre-operatively for localization of the sources of interictal epileptiform activity and somatosensory mapping. Spontaneous MEG was recorded with a 148 channel whole-head magnetometer (Magnes WH2500, 4-D Neuroimaging, San Diego, CA, USA) in a magnetically shielded room. Simultaneous EEG was recorded, with gold disc electrodes, using a bipolar montage (Neurofax, NihonKohden, Tokyo, Japan) from 21 scalp locations, placed according to the International 10-20 system. The MEG recordings were digitized at a sampling rate of 508 Hz. The on-line bandpass filter was set between 1-100 Hz. For optimal interictal analysis offline filtering was performed with a bandpass between 3 and 70 with a 60 Hz notch filter. The principles underlying MEG generation, recording, and source localization are reviewed elsewhere14-18.

As part of the analysis of the interictal paroxysmal activity, we calculated the equivalent current dipole (ECD) location, orientation and moment for each event. ECDs were computed at successive 2 msec intervals during the temporal evolution of the spike, using data from a set of 37 neighboring MEG sensors that contained both extrema of the magnetic flux distribution associated with each event. ECD solutions were considered acceptable if they met the following criteria:

1. A correlation coefficient of at least 0.98 (ensuring that the solution accounted for 96% or more of the observed magnetic flux distribution associated with each event).

2. A root mean square (RMS) of magnetic flux across all 37 channels of 400 fT or more.

3. A dipole moment (Q) under 400 nAm. An ECD sorting program was also applied for selecting the ECD with the best correlation coefficient for each event. This procedure results in a tighter cluster of ECDs, by retaining only the 'best' (i.e., presumably more reliable) solution for each event, from a series of contiguous ECDs that are likely to be modeling the same source19. More details on MEG data analyses can be found in a previous report from our group17,18.

Before the MRI scan was performed, three skin markers were placed at fiducial points on the patient's head (the nasion, the left and the right external meati). The location of the same fiducial points was also recorded, at the beginning of the MEG recording session, relative to the magnetometer sensor, thus establishing a common spatial reference for the transposition of 3-D coordinates between MEG and MRI data, as previously described

Electrocorticography

With the patient under general anesthesia, a left fronto-temporo-parietal craniotomy was performed. No gross abnormalities were apparent in the exposed cortex. A 64-contact subdural grid was placed over the fronto-parieto-temporal area. In addition, two six-- contact subdural strip electrodes were placed over left basal temporal areas. Long-term video-EEG monitoring was performed with these electrodes for a period of five days in order to capture a representative sample of paroxysmal activity associated with clinical seizures.

RESULTS

Magnetoencephalography

Frequent, large amplitude magnetic and electrical bursting epileptiform activity was noted predominantly over the left posterior frontal area on MEG and were recorded simultaneously on the surface EEG. The discharge trains occurred more frequently on MEG (Figure 1). Source localization of each burst of discharges was performed during three noncontiguous time windows, ranging in duration between 400 and 800 msec:

1. A window encompassing the onset of each burst.

2. A randomly selected window during the course of the burst.

3. A window capturing the last portion of each spike train.

ECD sources computed during each of the three time periods for a total of 72 discharge bursts overlapped anatomically, forming a large cluster of sources in the left inferior frontal and superior temporal lobes, extending into adjacent sensorimotor regions (Figure 2).

During the MEG recording session, ictal activity was registered for 20 sec before it developed into right sided facial twitching. Figure 3 shows that MEG paroxysmal discharges were more obvious and more frequent than EEG discharges. Reliable localization of ECD sources was successful at several time points during the ictal pattern just before it spread. The estimated sources of ictal activity were found near the center of FRBEA source clusters (Figure 2).

Electrocorticography

Ictal activity during the course of 13 recorded seizures showed a wide electrode distribution. In contrast, the distribution of activity at seizure onset was focal and confined to six electrode contacts (Figures 2 and 4). This region corresponded closely with the ictal focus derived from MEG. Further, the same contacts that defined the primary epileptogenic area also showed FRBEA interictally (Figure 1). This region was essentially coextensive with the distribution of the ECD cluster associated with magnetic rhythmic discharge bursts. However, the area that appeared to be generating interictal activity was larger than the ictal focus and this was true for both ECoG and MEG-derived localization data.

Surgery and post-operative course

Following the extra-operative video-EEG monitoring the patient underwent a repeat craniotomy under general anesthesia. At first, the presumed epileptogenic area, in the inferior frontal and superior temporal lobes, as determined by both ictal MEG and extra-operative ECoG, was resected. Histopathology of the resected tissue revealed giant neurons and balloon cells. Intraoperative ECoG recordings continued to show paroxysmal activity overlapping with part of the sensorimotor cortex superior to the resected area. Multiple subpial transection (MST) was performed in this region, instead of a corticectomy. All paroxysmal activity disappeared immediately after the MST. The patient's post-operative course was uneventful with the exception of a mild transient weakness in her right upper extremity.

At the most recent follow-up seven months after surgery the patient continues to be seizure-free and receives a single antiepileptic drug21. Her neurological examination is now normal, and her oral motor apraxia resolved when she stopped having daily seizures. She attends school and is performing at grade level.

DISCUSSION

Focal cortical dysplasia is commonly associated with partial seizures3,6,7,10, and complete removal of the epileptogenic zone can lead to significant clinical improvement10. However, given that the suspected epileptogenic zone often contains only microscopic abnormalities not detectable on MRI pre-operatively or by macroscopic examination of the exposed cortex7,22-26, it is difficult to determine the precise location and extent of the area to be resected10,23,27. At present, invasive electrophysiological recordings of ictal epileptiform discharges is the method of choice for pre-surgical planning in FCD. Noninvasive mapping techniques, like MSI which is in principle very accurate in localizing intracranial sources of neurophysiological activity13,16,28, could be particularly useful in the preoperative evaluation of FCD patients, provided that the following requirements are met:

1 . A sufficient sample of epileptiform activity is collected during the MEG recordings to permit reliable localization of these events.

2. This activity is generated within the primary epileptogenic zone.

3. The cortex generating these events is coextensive with the primary epileptogenic zone.

MSI relies primarily upon recordings of interictal epileptiform events that may not be constantly present in a given patient, and altogether absent in some patients. It is also possible that the cortical areas that generate interictal spikes and sharp waves (irritable zone) are not identical to the primary epileptogenic zone. Usually, the irritable zone is more extensive and may include a greater number of anatomically distinct cortical regions than the epileptogenic zone29. Although this may be quite common when the epileptiform activity available for a given patient consists of isolated, intermittent spikes and sharp waves, bursts of spikes occurring at a rate of 10 events per second or faster may provide a more reliable index of abnormal activity produced by the primary epileptogenic area3,10. Such bursts are a common occurrence in patients with FCD and may represent an intermediate stage between ictal and interictal state10. In fact, rhythmic spike discharges often precede the onset of ictal activity in some patients with FCD 2,6,10. Experimental studies are in agreement with these observations, showing increased excitatory events and reduced inhibitory influence generating longlasting seizure-like discharges . Our data clearly support this view, by showing that the area defined by the sources of FRBEA on MEG and the topography of similar events on extraoperative ECoG, was essentially identical to the primary epileptogenic region as determined by both ictal MEG and ECoG. This finding successfully addressed the first principal focus of the present investigation as outlined in the Introduction. The region that showed persistent, recurring epileptiform activity as indicated by the anatomical consistency of source localization during the temporal course of each spike burst coincided spatially with the extent of the cortex that contained microscopic abnormalities characterized by both prominent abnormal giant neurons and balloon cells on post-operative histological examination 32,33. This finding further supports the notion, indicating by extra-operative ECoG and acute depth electrode monitoring2,3,10, that epileptogenicity in FCD is intrinsic. Given that regional cortical pathology is (as in the case presented here) often not detectable on MRI, our data highlight the potential utility of MSI as a noninvasive tool for determining the location and extent of the epileptogenic zone in patients with FCD, provided that recordings of a sufficient sample of rhythmic epileptiform events, and subsequent reliable localization of their intracranial sources are feasible.

Our study is the first investigation that directly assessed the validity and accuracy of MSI-based localizations of both ictal and interictal epileptiform activity in FCD with reference to the `gold standard' in clinical practice, electrocorticography through chronically implanted subdural electrodes. It should be noted, however, that by using a single ECD model for source localization, the ictal onset zone was depicted by MSI as a single point, that was located near the geometric center of the ECoG ictal focus, in agreement with previous reports,15,34,35.

ACKNOWLEDGEMENTS

We wish to thank Ms Michele E. Fitzgerald for critical reading of this manuscript. We also thank Mr Eric Y. Caballero, 4-D Neuroimaging, Ms Pamela S. Zanek and Mr Mohammad Ayub, Epilepsy Monitoring Unit, Memorial Hermann Children's Hospital, for their technical assistance. This work was supported by NIH Grant R01 NS37941 to Andrew C. Papanicolaou.

REFERENCES

1 Brodtkorb E, Andersen K, Henriksen 0, Myhr G, Skullerud K. Focal, continuous spikes suggest cortical developmental abnormalities. Clinical, MRI and neuropathological correlates. Acta Neurol Scand 1998; 98: 377-385

2 Chassoux F, Devaux B, Landre E, Turak 13, Natal F, Varlet P, Chodkiewicz JP, Daumas-Duport C. Stereoelectroencephalography in focal cortical dysplasia: A 3D approach to delineating the dysplastic cortex. Brain 2000; 123: 1733-1751

3 Gambardella A, Pal mini A, Andermann F, Dubeau F, Da Costa JC, Quesney LF, Andermann E, Olivier A. Usefulness of focal rhythmic discharges on scalp EEG of patients with focal cortical dysplasia and intractable epilepsy. Electroencephalogr Clin Neurophysiol 1996; 98:243-249

4 Gondo K, Kira H, Tokunaga Y, Harashima C, Tobimatsu S,

Yamamoto T, Hara T. Reorganization of the primary somatosensory area in epilepsy associated with focal cortical dysplasia. Dev Med Child Neurol 2000; 42: 839-842

5 Minami T, Tasaki K, Yamamoto T, Gondo K, Yanai S, Ueda K. Magneto-encephalographical analysis of focal cortical heterotopia. Dev Med Child Neurol 1996; 38: 945-949

6 Morioka T, Nishio S, Ishibashi H, Muraishi M, Hisada K, Shigeto H, Yamamoto T, Fukui M. Intrinsic epileptogenicity of focal cortical dysplasia as revealed by magnetoencephalography and electrocorticography. Epilepsy Res 1999; 33: 177-187

7 Palmini A, Gambardella A, Andermann F, Dubeau F, da Costa JC, Olivier A, Tampieri D, Robitaille Y, Paglioli E, Paglioli Neto E, Coutinho L, Kim H. Operative strategies for patients with cortical dysplastic lesions and intractable epilepsy. Epilepsia 1994; 35 (Suppl. 6): 57-71

8 Quirk JA, Kendall B, Kingsley DP, Boyd SG, Pitt MC. EEG features of cortical dysplasia in children. Neuropediatrics 1993; 24: 193-199

9 Van Bogaert P, David P, Gillain CA, Wikler D, Damhaut P, Scalais E, Nuttin C, Wetzburger C, Szliwowski HB, Metens T, Goldman S. Perisylvian dysgenesis. Clinical, EEG, MRI and glucose metabolism features in 10 patients. Brain 1998; 121: 2229-2238

10 Palmini A, Gambardella A, Andermann F, Dubeau F, da Costa JC, Olivier A, Tampieri D, Gloor P, Quesney F, Andermann E, Paglioli E, Paglioli Neto E, Coutinho L, Leblanc R, Kim H. Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results. Ann Neurol 1995; 37: 476-487

11 Knowlton RC, Laxer KD, Aminoff MJ, Roberts TP, Wong ST, Rowley HA. Magnetoencephalography in partial epilepsy: Clinical yield and localization accuracy. Ann Neurol 1997; 42: 622-631

12 Paetau R, Kajola M, Karhu J, Nousiainen U, Partanen J, Tiihonen J, Vapalahti M, Hari R. Magnetoencephalographic localization of epileptic cortex - impact on surgical treatment. Ann Neurol 1992; 32: 106-109

13 Yamamoto T, Williamson SJ, Kaufman L, Nicholson C, Llinas R. Magnetic localization of neuronal activity in the human brain. Proc Natl Acad Sci USA 1988; 85: 8732-8736

14 Baumgartner C, Pataraia E, Lindinger G, Deecke L. Magnetoencephalography in focal epilepsy. Epilepsia 2000; 41 (Suppl. 3): 39-47

15 Ishibashi H, Morioka T, Shigeto H, Nishio S, Yamamoto T, Fukui M. Three-dimensional localization of subclinical ictal activity by magnetoencephalography: Correlation with invasive monitoring. Surg Neurol 1998; 50: 157-163

16 Ishibashi H, Morioka T, Nishio S, Shigeto H, Yamamoto T, Fukui M. Magnetoencephalographic investigation of somatosensory homunculus in patients with peri-Rolandic tumors. Neurol Res 2001; 23:29-38

17 Ishibashi H, Simos PG, Castillo EM, Maggio WW, Wheless JW, Kim HL, Venkataraman V, Sanders DK, Breier JI, Zhang W, Davis RN, Papanicolaou AC. Detection and significance of focal, interictal slow wave activity visualised by magnetoencephalography for localization of the primary epileptogenic region using magnetoencephalography. I Neurosurg 2002; 96: 724-730

18 Wheless JW, Willmore LJ, Breier JI, Kataki M, Smith JR, King DW, Meador KJ, Park YD, Loring DW, Clifton GL, Baumgartner J, Thomas AB, Constantinou JE, Papanicolaou AC. A comparison of magnetoencephalography, MRI, and V-EEG in patients evaluated for epilepsy surgery. Epilepsia 1999; 40: 931-941

19 Lewine JD, Orrison WW Jr. Spike and slow wave localization by magnetoencephalography. Neuroimaging Clin N Am 1665; 5: 575-596

20 Simos PG, Papanicolaou AC, Breier JI, Wheless JW, Constantinou JE, Gormley WB, Maggio WW. Localization of language-specific cortex by using magnetic source imaging and electrical stimulation mapping. J Neurosurg 1999; 91: 787-796

21 LUders H, Murphy D, Awad I, Wyllie E, Dinner DS, Morris III HH, Rothner AD. Quantitative analysis of seizure frequency 1 week and 6, 12, and 24 months after surgery of epilepsy. Epilepsia 1994; 35: 1174-1178

22 Chugani HT, Shewmon DA, Shields WD, Sankar R, Comair Y, Vinters HV, Peacock Wi. Surgery for intractable infantile spasms: Neuroimaging perspectives. Epilepsia 1993; 34: 764-771

23 Desbiens R, Berkovic SF, Dubeau F, Andermann F, Laxer KD, Harvey S, Leproux F, Melanson D, Robitaille Y, Kalnins R, Olivier A, Fabinyi G, Barbaro N. Life-threatening focal status epilepticus due to occult cortical dysplasia. Arch Neurol 1993; 50: 695-700

24 Duncan JS. Imaging and epilepsy. Brain 1997; 120: 339-377

25 Hirabayashi S, Binnie CD, Janota I, Polkey CE. Surgical treatment of epilepsy due to cortical dysplasia: Clinical and EEG findings. J Neurol Neurosurg Psychiatry 1993; 56: 765-770

26 Sisodiya SM, Free SL, Stevens JM, Fish DR, Shorvon SD. Widespread cerebral structural changes in patients with cortical dysgenesis and epilepsy. Brain 1995; 118: 1039-1050

27 Olivier A, Andermann F, Palmini A, Robitaille Y. Surgical treatment of the cortical dysplasias. In: Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin BG, Pfanner P, eds. Dysplasias of Cerebral Cortex and Epilepsy, Philadelphia: Lippencott-Raven, 1996: pp. 351-366

28 Ishibashi H, Tobimatsu S, Shigeto H, Morioka T, Yamamoto T, Fukui M. Differential interaction of somatosensory inputs in the human primary sensory cortex: A magnetoencephalographic study. Clin Neurophysiol 2000; 111: 1095-1102

29 Luders HO, Engel J Jr, Munari C. General principles. In: Engel J Jr, ed. Surgical Treatment of the Epilepsy. 2nd edn, New York: Raven Press, 1993: pp. 137-153

30 Ferrer I, Pineda M, Tallada M, Oliver B, Russi A, Oller L, Noboa R, Zujar MJ, Alcantara S. Abnormal local-circuit neurons in epilepsia partialis continua associated with focal cortical dysplasia. Acta Neuropathol (Berl) 1992; 83: 647-652

31 Mattia D, Olivier A, Avoli M. Seizure-like discharges recorded in human dysplastic neocortex maintained in vitro. Neurology 1995; 45:1391-1395

32 Palmini A, Andermann F, Olivier A, Tampieri D, Robitaille Y, Andermann E, Wright G. Focal neuronal migration disorders and intractable partial epilepsy: A study of 30 patients. Ann Neurol 1991; 30: 741-749

33 Taylor DC, Falconer MA, Bruton CJ, Corsellis JA. Focal dysplasia of the cerebral cortex in epilepsy. J Neurol Neurosurg Psychiatry 1971; 34:369-387

34 Stefan H, Schneider S, Abraham-Fuchs K, Bauer J, Feistel H, Pawlik G, Neubauer U, Rohrlein G, Huk WJ. Magnetic source localization in focal epilepsy. Multichannel magnetoencephalography correlated with magnetic resonance brain imaging. Brain 1990; 113: 1347-1359

35 Sutherling WW, Levesque MF, Crandall PH, Barth DS. Localization of partial epilepsy using magnetic and electric measurements. Epilepsia 1991; 32 (Suppl. 5): 29-40

Hideaki Ishibashi*, Panagiotis G. Simos*, James W. Wheless^^^, James E. Baumgartner(sec), Howard L. Kim^^, Eduardo M. Castillo*, Robert N. Davis* and Andrew C. Papanicolaou*

*Department of ^Neurosurgery, ^^Department of Neurology, (sec)Department of Pediatrics, Department of Pediatric Surgery (Neurosurgery), Vivian L Smith Center for Neurologic Research, Texas Comprehensive Epilepsy Program, The University of Texas Health Science Center at Houston, Houston, TX, USA

Correspondence and reprint requests to: Hideaki Ishibashi, MD, PhD, Department of Neurosurgery, University of Texas, Houston Medical School, 1333 Moursund St., Suite HI 114, Houston, TX 77030, USA. [Hideaki. Ishibashi@uth.tmc.edu] Accepted for publication May 2002.

Copyright Forefront Publishing Group Sep 2002
Provided by ProQuest Information and Learning Company. All rights Reserved

Return to Cortical dysplasia
Home Contact Resources Exchange Links ebay