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Aspects of Oral Language, Speech, and Written Language in Subjects with Temporal Lobe Epilepsy of Difficult Control

Abstract

Introduction

About 50 million people have epilepsy and 30% of them have epilepsy that does not respond to properly conducted drug treatment.

Objective

Verify the incidence of language disorders in oral language, speech, and written language of subjects with difficult to control temporal lobe epilepsy (TLE) and compare the occurrence of these disorders in subjects before and after surgery.

Methods

Cross-sectional study with quantitative analysis, exploratory type. A questionnaire for data collection was administered covering the following aspects: oral language, speech complaints, and writing production and comprehension. Criteria for inclusion of subjects were a diagnosis of TLE refractory to drug treatment and at least 4 years of schooling.

Results

The sample of 63 patients with TLE was divided into two groups: presurgical (n = 31) and postsurgical (n = 32). In the postsurgical group, there was a higher frequency of left lobectomy (75%) than right (25%).

Conclusion

Statistical analysis was performed with the chi-square test (significance level of 0.05). Complaints related to speech-language attention were more predominant in postsurgical subjects. Analysis of oral language, speech, and written language in subjects with epilepsy who underwent temporal lobectomy or not showed findings consistent with symptoms related to transient aphasia, with the presence of paraphasias, as well as changes in speech prosody and melody. These symptoms appeared more associated with recurrence after having a temporal lobectomy.

epilepsy; language; reading; speech-language and hearing sciences


Introduction

About 50 million people suffer from epilepsy with active seizures and 30% of them have refractory epilepsy (i.e., no response to properly conducted drug treatment).11 Epilepsy WHO. Epilepsy. Available at: http://www.who.int/mediacentre/factsheets/fs999/en/index.html. Accessed May 26, 2012
http://www.who.int/mediacentre/factsheet...
Temporal lobe epilepsy (TLE) is the most common form of epilepsy in adults. It is specific, with a high level of incidence and severity, and is characterized by the presence of simple and complex partial seizures. The temporal lobe can be divided into medial (playing an important role in episodic and autobiographical memory, coding, and temporal ordering of events in verbal memory, and visuospatial memory) as well as neocortical (related to semantic memory).22 Damasceno BP, Mitidieri ACH. Percepção do tempo em pacientes com epilepsia submetidos a lobectomia temporal anteromedial. Relatório Fapesp. Campinas SP, Brazil: Universidade Estadual de Campinas (UNICAMP); 2013.

Temporal lobectomy controls seizures in up to 70% of refractory epilepsy cases, but when found in the left hemisphere, it can impair oral language functions, especially related to naming.33 Bonelli SB, Thompson PJ, Yogarajah M, et al. Imaging language networks before and after anterior temporal lobe resection: results of a longitudinal fMRI study. Epilepsia 2012;53(4):639-650 Diminishment in verbal memory is also reported as a common effect after surgery on the dominant hemisphere of the temporal lobe.44 Tracy JI, Osipowicz K, Godofsky S, et al. An investigation of implicit memory through left temporal lobectomy for epilepsy. Neurobiol Learn Mem 2012;98(3):272-283 55 Lambon RMA, Ehsan S, Baker GA, Rogers TT. Semantic memory is impaired in patients with unilateral anterior temporal lobe resection for temporal lobe epilepsy. Brain. J Neurol 2012;135(1):242-258 66 Binder JR, Swanson SJ, Sabsevitz DS, Hammeke TA, Raghavan M, Mueller WM. A comparison of two fMRI methods for predicting verbal memory decline after left temporal lobectomy: language lateralization versus hippocampal activation asymmetry. Epilepsia 2010;51(4):618-626 77 Wagner K, Uherek M, Horstmann S, et al. Memory outcome after hippocampus sparing resections in the temporal lobe. J Neurol Neurosurg Psychiatry 2013;84(6):630-636 Studies show that patients who undergo temporal lobectomy may present deficits in semantic access in some tasks using work recovery.88 Protzner AB, McAndrews MP. Network alterations supporting word retrieval in patients with medial temporal lobe epilepsy. J Cogn Neurosci 2011;23(9):2605-2619 Examining the efficiency of lexical and semantic processing, in association with the activation of the brain, one realizes that a temporal lobectomy is associated with a failure in the functional organization of cortical networks involved in lexical and semantic processing.99 Jensen EJ, Hargreaves IS, Pexman PM, Bass A, Goodyear BG, Federico P. Abnormalities of lexical and semantic processing in left temporal lobe epilepsy: an fMRI study. Epilepsia 2011;52(11): 2013-2021

The resection of the temporal lobe can bring risks to verbal and visual episodic memory, as well as naming. Studies have reported declining naming and semantic functions postoperatively, suggesting the hypothesis that naming deficits arise from the functional specialization of the left temporal lobe and the semantic interpretation of visual input.1010 Hamberger MJ, Seidel WT, McKhann GM II, Goodman RR. Hippocampal removal affects visual but not auditory naming. Neurology 2010;74(19):1488-1493 1111 Schwarz M, Pauli E. Postoperative speech processing in temporal lobe epilepsy: functional relationship between object naming, semantics and phonology. Epilepsy Behav 2009;16(4):629-633 Studies pointed to the fact that patients with left resection showed anomia in simple semantic tasks and that with increasing complexity of the task, they showed semantic deficit.55 Lambon RMA, Ehsan S, Baker GA, Rogers TT. Semantic memory is impaired in patients with unilateral anterior temporal lobe resection for temporal lobe epilepsy. Brain. J Neurol 2012;135(1):242-258 Studies also have focused on brain reorganization for the processing of oral language during the postsurgical period.33 Bonelli SB, Thompson PJ, Yogarajah M, et al. Imaging language networks before and after anterior temporal lobe resection: results of a longitudinal fMRI study. Epilepsia 2012;53(4):639-650 1212 Tivarus ME, Starling SJ, Newport EL, Langfitt JT. Homotopic language reorganization in the right hemisphere after early left hemisphere injury. Brain Lang 2012;123(1):1-10 1313 Moser DC, Papanicolaou AC, Swank P, Breier JI. Evidence for the solidarity of the expressive and receptive language systems: a retrospective study. J Int Neuropsychol Soc 2011;17(1):62-68 In the preoperative period, aspects of determining the dominant hemisphere of oral language, which is critical in planning surgical procedures, are being investigated.1414 Pirmoradi M, Béland R, Nguyen DK, Bacon BA, Lassonde M. Language tasks used for the presurgical assessment of epileptic patients with MEG. Epileptic Disord 2010;12(2):97-108

Regarding written language, one study compared reading skills (comprehension and sentence recognition, as well as memory accuracy, fluency, and complexity) in patients after a left temporal resection with those from a control group.1515 Noppeney U, Price CJ, Duncan JS, Koepp MJ. Reading skills after left anterior temporal lobe resection: an fMRI study. Brain 2005;128 (Pt 6):1377-1385 Findings showed that, after surgery, proficiency in reading remains preserved due to a compensation mechanism of the right hemisphere coupled with integration of activated brain areas in the process.

Although surgical resection is common for the treatment of refractory TLE, the literature dealing with possible changes in oral language, speech, and written language in patients undergoing temporal lobectomy is scarce, a factor that justifies this study.

Considering the multidimensional impacts of epilepsy, including those that are linguistic and psychological, this study aims to verify the incidence of language disorders in oral language, speech, and writing language in subjects with TLE that is difficult to control and compare the occurrence of these disorders before and after surgery.

Methods

This is a cross-sectional, quantitative, exploratory study conducted in the Adult Epilepsy Clinic. This integrated epilepsy care program is a referral center in the Public Health System in Brazil and serves patients referred from various regions of the country. Clinic consultations occur in two stages: presurgical and postsurgical monitoring (∼40 consultations per month) and intractable epilepsy patients (∼180 consultations per month).

Evaluation

For data collection, a questionnaire with open and closed questions was given to subjects by a nurse and a speech therapist, averaging 30 minutes in duration. After that, a speech-language therapist applied a speech-language evaluation. Both tools have questions encompassing speech complaints, as well as speech and writing for both production and comprehension. Inclusion criteria for the study were having a diagnosis of refractory TLE (i.e., no response to properly conducted drug treatment) and at least 4 years of schooling. Patients who did not properly follow drug treatment or medical management were excluded. The questionnaire was answered after reading and signing the consent form.

Participants

The sample was comprised of 63 patients with TLE divided into two groups: presurgical (PRE-CIR; n = 31) and postsurgical (POS-CIR; n = 32). The PRE-CIR group was composed of 20 female (64.5%) and 11 male (35.5%) subjects with mean age of 40.4 years (standard deviation 12.7). In this group there was a higher prevalence of left TLE (n = 14), followed by right TLE (n = 9) and bilateral TLE (n = 8). The POS-CIR group was composed of 15 female (46.9%) and 17 male (53.1%) subjects, with mean age of 39.7 years (standard deviation 9.6). In this group there was a predominance of left TLE (n = 14), followed by right TLE (n = 9) and bilateral TLE (n = 8). There was a higher frequency of left lobectomy, 75% (n = 24), with right making up 25% (n = 8). The time interval between the temporal lobectomy and data collection ranged from 1 to 39 months.

Analysis

Statistical analysis was performed by applying the chi-square test (significance level p < 0.05).

Ethics

The project was approved by the Ethics Committee registration number 380977, CAAE: 18218413.9.0000.0096 of Sep 9, 2013.

Results

Of the total respondents, 68% presented with one or more aspects of interest to speech-language pathology and 62% had a change in the area of language. The aforementioned complaints were related to chewing, swallowing, hearing, vestibular system, and voice (Table 1).

Table 1
Distribution of the sample according to speech-language pathology complaints

Using the chi-square test, the POS-CIR group presented a more significant proportion of speech-language pathology complaints.

In the POS-CIR group, chewing alterations were more frequent, with 25% describing difficulty in opening their mouth (lasting 1 to 3 months after surgery). With swallowing, 6.2% reported pain for ∼20 days postoperatively. Tinnitus, ear pain, and ear fullness were cited as hearing issues by 21.9% of participants. Dizziness (3.1%) and weak vocal emissions (3.1%) were also identified among the complaints.

Frequent changes to speech production were speech rate (12.6%), prosody (8%), and speech intelligibility (8%). When comparing PRE-CIR and POS-CIR groups using the chi-square test, there was a significant difference only for the speech rate, with an appropriate speed being better among PRE-CIR subjects (Table 2). For the application of the test, the following variables were considered: phonological aspects, speech rate, prosody, as well as discourse understanding and structure.

Table 2
Distribution of the sample according to aspects of oral language and speech

To analyze possible changes in oral language related to the surgical procedure, pre- and postprocedure complaints (for POS-CIR) and current complaints (for PRE-CIR) were investigated. The subjects' responses were forgetting and missing words, anomia, paraphasia, memory loss, and stuttering (Table 3). Regarding these aspects, no significant differences between groups were observed. It is noteworthy that for application of the test, answers of none and no complaint were considered.

Table 3
Distribution of the sample according to oral language

From the perception of the subjects, alterations and/ or improvements in oral language and speech production and comprehension after surgery (POS-CIR) were investigated. The answers were classified as forgetting and missing words, anomia, paraphasia, memory loss, worsening of preexisting symptoms of stuttering/speech/memory, and difficulty in articulation (Table 4).

Table 4
Distribution of sample according to postsurgery oral language and speech complaints (n = 32)

Of the total POS-CIR subjects, 53% of participants reported some disorder. The most frequent complaints were forgetting and missing words (25%), paraphasia (12.5%), and worsening of preexisting symptoms of stuttering, speech, and memory (12.5%).

On the patient's perception of improvement in oral language and speech, after surgery, 12.5% reported feeling increased competence to speak and improvement in their emotional state to talk.

The relationship between oral language and speech disorders and surgery was not statistically significant, although a higher incidence of alterations was observed in patients with left TLE (Table 5).

Table 5
Relationship between aspects of speech and oral language and surgery side

Through the chi-square test, there was no significant difference in any case. To implement the test we considered the response categories: phonological aspects (omissions and distortions + substitutions), speech rate (adequate and fast + slow), prosody (adequate and monotone).

Results related to the reading and writing results are described in Table 6. There were no statistically significant differences between groups related to written language; however, the PRE-CIR group showed a higher percentage of disorders, with 16.1% in reading comprehension and 12.9% in writing production.

Table 6
Distribution of the sample according to aspects of reading and writing

Regarding disorders after surgery, 6.2% of participants reported difficulties related to the formal aspects (spelling) and 6.2% had difficulties understanding the written text.

Discussion

Complaints related to speech-language pathology were more predominant in POS-CIR subjects. It can be inferred that complaints related to chewing, swallowing, and hearing can be caused by the surgical procedure because the temporomandibular joint is composed of an articulating area whose concave depression lies in a portion of the temporal bone, an area manipulated during the lobectomy procedure, and is also in close proximity to the auditory system. Complaints regarding vocal ability may be related to the endotracheal or tracheal intubation procedure used for auxiliary support in artificial ventilation.

As for speech, the comparison between the POS-CIR and PRE-CIR groups showed statistically significant differences only for the alteration in rate of speech in the POS-CIR subjects. No studies that indicate similar findings were found.

There are references in the literature to the problems of speech production, as well as findings of our study, on the correlation between epilepsy and changes in prosody.1616 Peters AS, Rémi J, Vollmar C, Gonzalez-Victores JA, Cunha JP, Noachtar S. Dysprosody during epileptic seizures lateralizes to the nondominant hemisphere. Neurology 2011;77(15):1482-1486 In addition, regarding oral language, both groups presented alterations as missing words, anomia, paraphasia, memory loss, and stuttering.

According to the literature, it appears that TLE has been associated with such alterations because the epileptogenic zone is located in the temporal lobe dominant for such functions. And TLE is also associated with dysfunction in memory when it involves the temporal lobes of both hemispheres.1717 Rzezak P, Fuentes D, Guimarães CA, Guerreiro M, Valente KDR. A Disfunção do Lobo Frontal em Crianças e Adolescentes com Epilepsia de Lobo Temporal e sua Possível Correlação com a Ocorrência de Transtornos Psiquiátricos. J Epilepsy Clinical Neurophysiol 2005;11(3):131-136 The occurrence of symptoms classified as forgetting and missing words are frequently reported by patients with TLE.1818 Guimarães CA, Min LL, Rzezak P. Memory impairment in children with temporal lobe epilepsy: a review. J Epilepsy Clinical Neurophysiol 2006;12(1):22-25 1919 Trebuchon-Da Fonseca A, Guedj E, Alario FX, et al. Brain regions underlying word finding difficulties in temporal lobe epilepsy. Brain 2009;132(Pt 10):2772-2784

In our study, we found that paraphasias corroborated another study in which, after having a temporal lobectomy, patients identified deficits in semantic retrieval tasks with words, showing paraphasias.88 Protzner AB, McAndrews MP. Network alterations supporting word retrieval in patients with medial temporal lobe epilepsy. J Cogn Neurosci 2011;23(9):2605-2619

Naming difficulties also were described in the literature after left temporal lobe surgery.33 Bonelli SB, Thompson PJ, Yogarajah M, et al. Imaging language networks before and after anterior temporal lobe resection: results of a longitudinal fMRI study. Epilepsia 2012;53(4):639-650 2020 Bartha L, Trinka E, Ortler M, et al. Linguistic deficits following left selective amygdalohippocampectomy: a prospective study. Epilepsy Behav 2004;5(3):348-357 2121 Sabsevitz DS, Swanson SJ, Hammeke TA, et al. Use of preoperative functional neuroimaging to predict language deficits from epilepsy surgery. Neurology 2003;60(11):1788-1792 Naming deficits were observed only in patients with left TLE and yet a significant association was found between the decline of postoperative naming and prejudice to semantic functions.1111 Schwarz M, Pauli E. Postoperative speech processing in temporal lobe epilepsy: functional relationship between object naming, semantics and phonology. Epilepsy Behav 2009;16(4):629-633 Naming has been identified in regions of the cortex involved in oral language. Studies show that patients with TLE have no difficulty in naming concrete objects that were visually presented to them. However, before and after surgery, they often show difficulty in finding words in their daily activities (forgetting/missing words, anomia).2222 Powell HW, Parker GJ, Alexander DC, et al. Imaging language pathways predicts postoperative naming deficits. J Neurol Neurosurg Psychiatry 2008;79(3):327-330

As with the findings of this study, previous research found that TLE is associated with alterations to the functioning of episodic long-term memory, and recovery processes and immediate recognition (short-term memory) appear less affected.2323 Hamberger MJ, Seidel WT, McKhann GM II, Perrine K, Goodman RR. Brain stimulation reveals critical auditory naming cortex. Brain 2005;128(Pt 11):2742-2749 2424 Busch NA, Groh-Bordin C, Zimmer HD, Herrmann CS. Modes of memory: early electrophysiological markers of repetition suppression and recognition enhancement predict behavioral performance. Psychophysiology 2008;45(1):25-35 2525 Yancey SW, Phelps EA. Functional neuroimaging and episodic memory: a perspective. J Clin Exp Neuropsychol 2001;23(1): 32-48 The effect of epilepsy on memory and forgetting words is better understood in mesial TLE with hippocampal sclerosis, because the hippocampus and entorhinal cortex neighbors are involved in the formation of declarative memory. As the verbal episodic memory is strongly associated with the dominant hemisphere, patients with left mesial TLE, in general, exhibit deficits in consolidation and recovery of verbal memory. In cases where the epileptic focus is located in the nondominant hemisphere, visuospatial memory may be affected.2626 Dickerson BC, Eichenbaum H. The episodic memory system: neurocircuitry and disorders. Neuropsychopharmacology 2010; 35(1):86-104

One study demonstrated the link between problems with long-term memory and TLE, because the mesial temporal lobe plays a prominent role in memory.2727 Oliveira GNM, Kummer A, Salgado JV, Marchetti Rl, Teixeira AL. Transtornos Neuropsiquiátricos da Epilepsia do Lobo Temporal. Rev Bras Neurol 2009;45(1):15-23 Subjects with TLE tend to show amnesic alterations.2828 Hendriks MPH, Aldenkamp AP, Alpherts WC, Ellis J, Vermeulen J, van der Vlugt H. Relationships between epilepsy-related factors and memory impairment. Acta Neurol Scand 2004;110(5): 291-300 Other aspects of amnesic function may be factors such as remote, autobiographical, and semantic memory.2929 Hötting K, Katz-Biletzky T, Malina T, Lindenau M, Bengner T. Longterm versus short-term memory deficits for faces in temporal lobe and generalized epilepsy patients. J Int Neuropsychol Soc 2010; 16(3):574-578

Most participants still had fluent reading skills and comprehension, and there was no significant difference between PRE-CIR and POST-CIR in aspects of reading and reading comprehension, which corroborates with the literature.1515 Noppeney U, Price CJ, Duncan JS, Koepp MJ. Reading skills after left anterior temporal lobe resection: an fMRI study. Brain 2005;128 (Pt 6):1377-1385 A higher occurrence of changes related to reading comprehension and written production was cited by the PRE-CIR group, corroborating prior studies.3030 Bell BD, Giovagnoli AR. Recent innovative studies of memory in temporal lobe epilepsy. Neuropsychol Rev 2007;17(4):455-476 3131 Butterbaugh G, Olejniczak P, Roques B, et al. Lateralization of temporal lobe epilepsy and learning disabilities, as defined by disability-related civil rights law. Epilepsia 2004;45(8):963-970

Conclusion

In the analysis of aspects of oral language, speech, and written language, subjects with epilepsy who did or did not undergo a temporal lobectomy showed findings consistent with the symptoms related to transient aphasia, with the presence of paraphasias, as well as changes in speech prosody and melody. These symptoms are peculiar and appear with higher frequency when associated with temporal lobectomy surgery. The study highlighted the need to implement research that addresses implications in speech and written language sciences for people with epilepsy.

References

  • 1
    Epilepsy WHO. Epilepsy. Available at: http://www.who.int/mediacentre/factsheets/fs999/en/index.html. Accessed May 26, 2012
    » http://www.who.int/mediacentre/factsheets/fs999/en/index.html
  • 2
    Damasceno BP, Mitidieri ACH. Percepção do tempo em pacientes com epilepsia submetidos a lobectomia temporal anteromedial. Relatório Fapesp. Campinas SP, Brazil: Universidade Estadual de Campinas (UNICAMP); 2013.
  • 3
    Bonelli SB, Thompson PJ, Yogarajah M, et al. Imaging language networks before and after anterior temporal lobe resection: results of a longitudinal fMRI study. Epilepsia 2012;53(4):639-650
  • 4
    Tracy JI, Osipowicz K, Godofsky S, et al. An investigation of implicit memory through left temporal lobectomy for epilepsy. Neurobiol Learn Mem 2012;98(3):272-283
  • 5
    Lambon RMA, Ehsan S, Baker GA, Rogers TT. Semantic memory is impaired in patients with unilateral anterior temporal lobe resection for temporal lobe epilepsy. Brain. J Neurol 2012;135(1):242-258
  • 6
    Binder JR, Swanson SJ, Sabsevitz DS, Hammeke TA, Raghavan M, Mueller WM. A comparison of two fMRI methods for predicting verbal memory decline after left temporal lobectomy: language lateralization versus hippocampal activation asymmetry. Epilepsia 2010;51(4):618-626
  • 7
    Wagner K, Uherek M, Horstmann S, et al. Memory outcome after hippocampus sparing resections in the temporal lobe. J Neurol Neurosurg Psychiatry 2013;84(6):630-636
  • 8
    Protzner AB, McAndrews MP. Network alterations supporting word retrieval in patients with medial temporal lobe epilepsy. J Cogn Neurosci 2011;23(9):2605-2619
  • 9
    Jensen EJ, Hargreaves IS, Pexman PM, Bass A, Goodyear BG, Federico P. Abnormalities of lexical and semantic processing in left temporal lobe epilepsy: an fMRI study. Epilepsia 2011;52(11): 2013-2021
  • 10
    Hamberger MJ, Seidel WT, McKhann GM II, Goodman RR. Hippocampal removal affects visual but not auditory naming. Neurology 2010;74(19):1488-1493
  • 11
    Schwarz M, Pauli E. Postoperative speech processing in temporal lobe epilepsy: functional relationship between object naming, semantics and phonology. Epilepsy Behav 2009;16(4):629-633
  • 12
    Tivarus ME, Starling SJ, Newport EL, Langfitt JT. Homotopic language reorganization in the right hemisphere after early left hemisphere injury. Brain Lang 2012;123(1):1-10
  • 13
    Moser DC, Papanicolaou AC, Swank P, Breier JI. Evidence for the solidarity of the expressive and receptive language systems: a retrospective study. J Int Neuropsychol Soc 2011;17(1):62-68
  • 14
    Pirmoradi M, Béland R, Nguyen DK, Bacon BA, Lassonde M. Language tasks used for the presurgical assessment of epileptic patients with MEG. Epileptic Disord 2010;12(2):97-108
  • 15
    Noppeney U, Price CJ, Duncan JS, Koepp MJ. Reading skills after left anterior temporal lobe resection: an fMRI study. Brain 2005;128 (Pt 6):1377-1385
  • 16
    Peters AS, Rémi J, Vollmar C, Gonzalez-Victores JA, Cunha JP, Noachtar S. Dysprosody during epileptic seizures lateralizes to the nondominant hemisphere. Neurology 2011;77(15):1482-1486
  • 17
    Rzezak P, Fuentes D, Guimarães CA, Guerreiro M, Valente KDR. A Disfunção do Lobo Frontal em Crianças e Adolescentes com Epilepsia de Lobo Temporal e sua Possível Correlação com a Ocorrência de Transtornos Psiquiátricos. J Epilepsy Clinical Neurophysiol 2005;11(3):131-136
  • 18
    Guimarães CA, Min LL, Rzezak P. Memory impairment in children with temporal lobe epilepsy: a review. J Epilepsy Clinical Neurophysiol 2006;12(1):22-25
  • 19
    Trebuchon-Da Fonseca A, Guedj E, Alario FX, et al. Brain regions underlying word finding difficulties in temporal lobe epilepsy. Brain 2009;132(Pt 10):2772-2784
  • 20
    Bartha L, Trinka E, Ortler M, et al. Linguistic deficits following left selective amygdalohippocampectomy: a prospective study. Epilepsy Behav 2004;5(3):348-357
  • 21
    Sabsevitz DS, Swanson SJ, Hammeke TA, et al. Use of preoperative functional neuroimaging to predict language deficits from epilepsy surgery. Neurology 2003;60(11):1788-1792
  • 22
    Powell HW, Parker GJ, Alexander DC, et al. Imaging language pathways predicts postoperative naming deficits. J Neurol Neurosurg Psychiatry 2008;79(3):327-330
  • 23
    Hamberger MJ, Seidel WT, McKhann GM II, Perrine K, Goodman RR. Brain stimulation reveals critical auditory naming cortex. Brain 2005;128(Pt 11):2742-2749
  • 24
    Busch NA, Groh-Bordin C, Zimmer HD, Herrmann CS. Modes of memory: early electrophysiological markers of repetition suppression and recognition enhancement predict behavioral performance. Psychophysiology 2008;45(1):25-35
  • 25
    Yancey SW, Phelps EA. Functional neuroimaging and episodic memory: a perspective. J Clin Exp Neuropsychol 2001;23(1): 32-48
  • 26
    Dickerson BC, Eichenbaum H. The episodic memory system: neurocircuitry and disorders. Neuropsychopharmacology 2010; 35(1):86-104
  • 27
    Oliveira GNM, Kummer A, Salgado JV, Marchetti Rl, Teixeira AL. Transtornos Neuropsiquiátricos da Epilepsia do Lobo Temporal. Rev Bras Neurol 2009;45(1):15-23
  • 28
    Hendriks MPH, Aldenkamp AP, Alpherts WC, Ellis J, Vermeulen J, van der Vlugt H. Relationships between epilepsy-related factors and memory impairment. Acta Neurol Scand 2004;110(5): 291-300
  • 29
    Hötting K, Katz-Biletzky T, Malina T, Lindenau M, Bengner T. Longterm versus short-term memory deficits for faces in temporal lobe and generalized epilepsy patients. J Int Neuropsychol Soc 2010; 16(3):574-578
  • 30
    Bell BD, Giovagnoli AR. Recent innovative studies of memory in temporal lobe epilepsy. Neuropsychol Rev 2007;17(4):455-476
  • 31
    Butterbaugh G, Olejniczak P, Roques B, et al. Lateralization of temporal lobe epilepsy and learning disabilities, as defined by disability-related civil rights law. Epilepsia 2004;45(8):963-970

Publication Dates

  • Publication in this collection
    Oct-Dec 2015

History

  • Received
    10 Dec 2014
  • Accepted
    26 Jan 2015
Fundação Otorrinolaringologia R. Teodoro Sampaio, 483, 05405-000 São Paulo/SP Brasil, Tel.: (55 11) 3068-9855, Fax: (55 11) 3079-6769 - São Paulo - SP - Brazil
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