Published online Jan 19, 2022. doi: 10.5498/wjp.v12.i1.98
Peer-review started: February 28, 2021
First decision: September 5, 2021
Revised: September 25, 2021
Accepted: December 2, 2021
Article in press: December 2, 2021
Published online: January 19, 2022
The pathogenesis of temporal lobe epilepsy (TLE) was originally considered to be acquired. However, some reports showed that TLE was clustered in some families, indicating a genetic etiology. With the popularity of genetic testing technology, eleven different types of familial TLE (FTLE), including ETL1-ETL11, have been reported, of which ETL9-ETL11 had not yet been included in the OMIM database. These types of FTLE were caused by different genes/Loci and had distinct characteristics. ETL1, ETL7 and ETL10 were characterized by auditory, visual and aphasia seizures, leading to the diagnosis of familial lateral TLE. ETL2, ETL3 and ETL6 showed prominent autonomic symptom and automatism with or without hippocampal abnormalities, indicating a mesial temporal origin. Febrile seizures were common in FTLEs such as ETL2, ETL5, ETL6 and ETL11. ETL4 was diagnosed as occipitotemporal lobe epilepsy with a high incidence of migraine and visual aura. Considering the diversity and complexity of the symptoms of TLE, neurologists enquiring about the family history of epilepsy should ask whether the relatives of the proband had experi
Core Tip: Eleven types of familial temporal lobe epilepsy (FTLE) caused by single gene mutations or specific gene loci had been identified to date. The phenotype of FTLE was heterogenous and includes typical temporal lobe seizures and specific symptoms. We herein describe the etiology, inheritance, phenotype and prognosis of each type of FTLE and summarize their similarities and differences.
- Citation: Liu C, Qiao XZ, Wei ZH, Cao M, Wu ZY, Deng YC. Molecular typing of familial temporal lobe epilepsy. World J Psychiatry 2022; 12(1): 98-107
- URL: https://www.wjgnet.com/2220-3206/full/v12/i1/98.htm
- DOI: https://dx.doi.org/10.5498/wjp.v12.i1.98
Epilepsy is a disorder of the brain characterized by an enduring predisposition to generate two unprovoked seizures > 24 h apart[1]. Epilepsy could be classified as focal, generalized, combined generalized and focal, and unknown according to the origin of the seizures[2]. Epilepsy affected approximately 50 million people worldwide, among which up to 60%-70% of affected individuals had focal epilepsy[3,4]. Epilepsy and its comorbidities, such as memory and psychiatric disorders, severely lower the quality of life of patients[5]. Temporal lobe epilepsy (TLE), including mesial TLE (MTLE) and lateral TLE (LTLE), was the most common type of focal epilepsy, especially in adults[6]. The causes of TLE were heterogeneous, and the overall prognosis of TLE was far from satisfactory[7].
The first description of an instance of familial TLE (FTLE) could be traced back to 1895, before TLE had been defined[8,9]. In 1994, Berkovic et al[10] provided the first report of familial TLE, in which four individuals in two generations were diagnosed with TLE. The family aggregation of TLE indicated a genetic etiology. Although the characteristics of TLE had been extensively studied, the genetic etiology of TLE remains unclear, and the incidence of FTLE were severely underestimated due to the high rates of misdiagnosis and missed diagnosis in individuals with subtle symptoms[11]. Leucine-rich glioma inactivated-1 (LGI1) mutations was identified in approximately 50% of families with LTLE and 3% of sporadic LTLE cases[12, 13]. Those findings had led to the hypothesis that LTLE was commonly caused by gene mutations and promoted the exploration of the genetic causes of LTLE[14]. Seventy percent of MTLE cases were considered to be caused by hippocampal sclerosis (HS) and was drug-refractory[15]. Most patients with drug-refractory MTLE had to undergo costly surgery, although 30% of such patients experience relapse within two years[16]. Many reports had shown that HS and MTLE were inheritable[17,18]. The mechanism seemed polygenic and was affected by multiple factors[19]. Further exploration of the underlying pathogenic genes and molecular mechanisms was critical for precision medicine.
Eleven genes/Loci responsible for FTLE have been reported to date (Table 1), including the genes LGI1, carboxypeptidase A6 (CPA6), reelin (RELN), galanin and GMAP prepropeptide (GAL), DEP domain containing 5 (DEPDC5), microtubule associated monooxygenase, calponin and LIM domain containing 1 (MICAL-1) and sodium voltage-gated channel alpha subunit 1 (SCN1A), along with gene loci on chromosomes (Chr) 12q22-q23.3, 4q13.2-q21.3, 9q21-q22, and 3q25-q26. These genes were involved in different biological processes. In this article, we describe the research progress on eleven types of FTLE, ETL1-ETL11, caused by these genes/Loci, of which ETL9-ETL11 had not yet been recorded in the OMIM database.
| Phenotype | OMIM ID | Gene/locus | Inheritance | Age at seizure onset (yr) | Seizure types | EEG | MRI | Epilepsy types | Prognosis | Ref. |
| ETL1 | 600512 | LGI1 | AD | 4-50 | Aud, Aph, FBTCS | T ea | Nor | LTLE | Responsive to ASM | [20,24,25] |
| ETL2 | 608096 | Chr12q22-q23.3 | AD | 0.75-35 | FS, FBTCS; Cog, Aut | Nor, T ea | HM | MTLE | Responsive to ASM or SR | [27,28] |
| ETL3 | 611630 | Chr4q13.2-q21.3 | AD | 5-18 | Cog, FBCTS, FIAS | Nor, T ea | Nor | MTLE | Responsive to ASM or SR | [32] |
| ETL4 | 611631 | Chr9q21-q22 | AD | 0.58-63 | Focal Mot; Cog, Sen, Aut, FIAS, FBCTS | Nor | Nor | OTLE | Responsive to ASM or SR; migraine 5/Mo – 2/y | [33] |
| ETL5 | 614417 | CPA6 | AR | 0.75-5 | FS, FBECTS, FIAS | T ea | T atr, HS | TLE | Responsive to ASM or SR | [36] |
| AD | 1.25-23 | FS | - | T atr | TLE | Drug-refractory | [36] | |||
| ETL6 | 615697 | Chr3q25-q26 | AD | 3-46 | FS, FIAS, Cog, Sen, Aut, FBTCS | Nor, T ea, sa | Nor | MTLE | Responsive to ASMs | [37] |
| ETL7 | 616436 | RELN | AD | 8-40 | Vis, Aud, FBECTS, FIAS | T ea | Nor | LTLE | Responsive to ASM or SR | [38,40] |
| ETL8 | 616461 | GAL | AD | 13 | FIAS, Cog, Sen, Aut, FBTCS | T ea | Nor | TLE | Responsive to ASM | [43] |
| ETL9 | - | DEPDC5 | AD | 8-13 | FS,Cog, Sen,focal Mot; FBECTS | T ea | Nor | TLE | Responsive to ASM | [44,46,47] |
| ETL10 | - | MICAL-1 | AD | 6-30 | Aud, Aph, FBECTS | T or FT ea | Nor | LTLE | Responsive to ASM | [48] |
| ETL11 | - | SCN1A | AD | 10-13 | FS, FIAS, Aut; focal Mot, FBECTS | T ea | HS | TLE | Responsive to ASM | [50] |
ETL1 (OMIM 600512) was first reported by Ottman et al[20] in a family in which 11 members in three generations had seizures, with most seizures having auditory features, suggesting a neocortical (or lateral) temporal lobe origin. Linkage analysis revealed that the candidate epilepsy gene was located on Chr 10q22–q24. In 2002, an LGI1 gene mutation on Chr 10q22–q24 was identified as the pathogenic cause[21]. LGI1 is a 60-kDa secreted protein that is predominantly expressed in neuronal cells in the brain and is involved in cortical neuronal migration, neuronal excitability and synaptic transmission. LGI1 mutations could lead to protein folding failure and destroy the interaction with its ligand, ADAM22[22].
More than 40 LGI1 variants related to ETL1 had been detected to date[23]. The variants were usually inherited from the affected parents and were rarely de novo, and the overall penetrance of the disorder was 61%-67%. The age of seizure onset was 4-50 years, usually 12-30 years[24]. Auditory and/or sensory aphasia seizures were the most common seizure types, and interictal electroencephalogram (EEG) showed temporal lobe origin, which supports the diagnosis of LTLE. The auditory symptoms ranged from unformed sounds, such as humming and ringing, to distortions and volume changes. Autonomic symptoms were less common. Most patients had experienced focal to bilateral tonic-clonic seizures (FBCTS). The prognosis was good with anti-seizure medications (ASMs), such as phenytoin and carbamazepine[25]. Some research has shown that treatment with the chemical corrector 4-phenylbutylate ameliorates the increased seizure susceptibility of LGI1 mutant mice, which provides potential new therapeutic options for LGI1-mediated epilepsy[26].
Depondt et al[27] reported a 5-generation family in which 22 members had TLE and febrile seizures without HS. Claes et al[28] linked this phenotype, namely, ETL2 (OMIM 608096), to Chr 12q22-q23.3, which includes 280 genes. ETL2 was autosomal dominant inherited, and the penetrance was approximately 80%. Those patients had a high incidence of febrile seizures, and all febrile seizures disappeared before 6 years of age. The mean age at onset of afebrile seizures was 8 years. The most common seizure types included focal seizures with or without impaired awareness, such as sensation in the head, fear, confusion and viscerosensory and tonic-clonic seizures. Ten of the patients were diagnosed with MTLE. Hippocampal malrotation was common in this family, even in individuals without seizures. The prognosis was good, with 11 individuals experiencing spontaneous remission. In addition, there was a report of a family in which seven members had febrile seizures that evolved to tonic-clonic seizures. The genetic linkage analysis mapped to Chr 12q22-q23.3[29]. Recently, Maria et al[30] reported a sporadic case with TLE and febrile seizures who had a 12 Mb duplication at Chr12q22-q23.3. She presented with growth retardation. Her seizure was well controlled with carbamazepine. These findings indicated that Chr 12q22-q23.3 had a broad phenotypic spectrum, similar to most well-known epileptogenic genes[31]. The symptoms of patients from the same family showed high similarity, which might be related to the common mutation sites and genetic backgrounds. The exact pathogenic mechanism required further research.
Hedera et al[32] reported a 4-generation family in which 11 individuals were diagnosed with MTLE or ETL3 (OMIM 611630). Linkage analysis mapped the phenotype to Chr 4q13.2-q21.3, which include 359 genes without homology to the well-known epileptic genes. ETL3 showed autosomal dominant inheritance with incomplete penetrance. The age of seizure onset was 5-18 years and most patients were 10-20 years. Ten individuals had focal cognitive seizures with feelings of déjà vu associated with dizziness or nausea, and 8 also had focal seizures with altered awareness and staring. Four individuals had FBCTS. Brain magnetic resonance imaging (MRI) was performed on 3 patients and the findings were not significant. EEG was performed on 6 patients, of whom 5 patients exhibited normal EEG and 1 had left anterior temporal sharp waves. Only 4 patients were treated with ASMs.
ETL4 (OMIM 611631) was reported in a 5-generation family of which 14 individuals had occipitotemporal lobe epilepsy and migraine with visual aura[33]. Genome-wide linkage and haplotype analysis mapped the phenotype to Chr 9q21-q22, which include 604 genes. ETL4 was autosomal dominant and was inherited with a low penetrance of 75%. The age at seizure onset ranged from 7 mo to 63 years, and the median age was 21 years. Age at migraine onset ranged from 30 to 65 years, with a median age of 42 years. Ten individuals had occipitotemporal lobe epilepsy and 5 of them also had migraine with aura. Nine of the 10 patients had focal motor or nonmotor seizures, such as visual, autonomic, and somatosensory symptoms, olfactory and auditory hallucinations, and cognitive seizures excluding déjà vu. Three of the 10 patients had focal seizures with altered awareness and 3 had FBCTS. Four had a single isolated seizure, and 1 of them also had migraine with aura. Seizures and migraine attacks were temporally independent in all patients except one. EEG and brain MRI were normal except in 2 patients with age-related white matter changes.
Approximately 6% of migraine patients have seizures, and 8%-15% of epilepsy patients have migraines[34]. Tikka-Kleemola et al[35] reported that among 33 families of patients experiencing migraine with visual aura, 22 families were linked to Chr 9q21-q22. None of these family members had seizures. These findings indicated that epilepsy and migraine have a common genetic basis and that Chr 9q21-q22 was closely related to epilepsy and migraine.
Salzmann et al[36] reported four children with recessive familial forms of febrile seizures and TLE born to healthy first-cousin parents. A CPA6 gene homozygous mutation was found associated with the phenotype and was named ETL5 (OMIM 614417). All 4 patients had febrile seizure onset before 4 years of age. One of them had TLE. His MRI showed right temporal atrophy, and EEG showed right temporal spikes and waves. They all became seizure-free with or without ASMs. In vitro research showed that CPA6 variants reduced the level of protein expression and secretion and/or destroyed carboxypeptidase activity. Salzmann et al[36] also reported a sporadic case with drug-refractory TLE carrying compound heterozygous mutations in the CPA6 gene. MRI showed cavernous malformation. His grandfather had a history of febrile seizures. Four unrelated patients with febrile seizures and refractory TLE carrying CPA6 gene heterozygous mutations were also reported, suggesting that ETL5 was both recessively and dominantly inherited[36]. The seizure onset of these 4 patients ranged from 15 mo to 23 years of age. Among them, one had febrile seizures and left temporal lobe origin seizures with HS. His brother had a history of febrile seizures. Two patients had temporal lobe seizures originating from the temporoparietal junction and bitemporal lobes. These two patients had neonatal sequelae and bitemporal atrophy on MRI. The last patient had febrile seizures, and his mother also had a history of febrile seizures. The prognosis of patients with homozygous mutations seemed to be better than that of patients with heterozygous mutations.
Only one ETL6 (OMIM 615697) family had been reported to date by Chahine et al[37] in 2013. In the 4-generation family surveyed in the study, 7 individuals had TLE, and 4 had febrile seizures during childhood but no subsequent epilepsy. Genetic linkage analysis linked the phenotype to Chr 3q25-q26 containing 453 genes. ETL6 was autosomal dominant and inherited with incomplete penetrance. The age of onset of temporal seizures ranged from 3 to 46 years. The 4 patients with isolated febrile seizures had onset between 5 mo to 5 years of age. Seizure types included focal aware seizures, focal impaired awareness seizures, FBCTS and rarely status epilepticus. Many of the seizures were suggestive of a mesial temporal origin, and occurred with auras including abdominal discomfort, rising numbness, floating sensation, strange grabbing feeling, déjà vu and dizziness. Brain MRI, performed in 3 patients, was normal. EEG was normal except in 1 patient who exhibited sharp right temporal waves and irregular slow activity. The seizures of the patients were responsive to ASMs.
Dazzo et al[38] identified seven different heterozygous missense mutations in the RELN gene in 7 unrelated families with LTLE or ETL7 (OMIM 616436). The RELN gene is crucial for the correct cytoarchitecture of laminated structures during embryonic development and modulates dendritic growth and synaptic plasticity in the postnatal and adult stages[39]. Their research revealed that the expression of reelin was reduced in the hippocampus of ETL7 patients and reelin promoter methylation was greater with severe granule cell dispersion, which supports a compromised reelin signaling pathway and identifies promoter methylation as an epigenetic mechanism in the pathogenesis of ETL7[38]. The clinical features of ETL7 were found to be similar to those of ETL1[40]. The mean age at seizure onset was 20 years. Seizure types included focal visual seizures, auditory seizures, déjà vu, FBTCS and focal seizures with impairment of consciousness. These patients were seizure-free with or without ASMs treatment. Previous work revealed that homozygous RELN gene mutations caused lissencephaly with cerebellar hypoplasia[41]. Three small consanguineous LCH-affected families had been reported thus far. The heterozygous individuals in these families exhibited reduced levels of reelin in their sera and were reported to be clinically normal[42]. The apparent normal phenotype of these individuals was consistent with the low penetrance of RELN mutations.
ETL8 (OMIM 616461) was reported by Guipponi et al[43] in a pair of monozygotic twin brothers with TLE carrying a heterozygous missense mutation in the GAL gene. The GAL gene encodes galanin, which is a neuropeptide highly expressed in the central nervous system. The mutant galanin identified in their study led to antagonistic activity against GALR1-mediated responses, decreased binding affinity and reduced agonist properties for GALR2 in vitro, suggesting that the variants impaired galanin signaling in the hippocampus and led to increased glutamatergic excitation[43]. The age of seizure onset was 13 years in both patients. Both had focal abdominal sensory seizures, incoherent speech, blurred vision, auditory hallucinations, slow ideation déjà vu and occasional FBCTS. Brain MRI findings were normal. Seizures were well controlled by ASMs.
In 2013, Shida et al[44] reported two families with TLE caused by DEPDC5 gene heterogenous mutations. The patients had focal nonmotor and motor seizures and their interictal EEG showed slow waves and sharp waves in the temporal lobes[45]. DEPDC5 proteins have no homology with ion channel proteins. DEPDC5 protein formed a GATOR1 complex with NPRL2 and NPRL3, which inhibited the aggregation of mTORC1. In vitro, mutant mRNA products are degraded by the nonsense-mediated decay system, and DEPDC5 haploinsufficiency was likely to be the cause of the disease[44]. Striano et al[46] detected a DEPDC5 gene nonsense mutation, p.Tyr306*, in a family with two individuals diagnosed with MTLE. In the proband and her mother, the seizures were characterized by déjà vu, anxiety, derealization and epigastric sensation. During follow-up, the proband showed significant auditory seizures weekly, suggesting a diagnosis of LTLE[47]. The reports to date indicated that the phenotype of DEPDC5-related TLE was variable and that DEPDC5 variants were responsible for both MTLE and LTLE.
Dazzo et al[48] identified three different MICAL-1 gene heterozygous missense mutations in three LTE families without LGI1 or RELN gene mutations. The MICAL-1 gene is expressed ubiquitously, with higher expression levels in the embryonic and nervous systems. In vitro, the variants significantly increased MICAL-1 oxidoreductase activity and induced cell contraction, which likely resulted from deregulation of F-actin dynamics[49]. These results suggested that the dysregulation of actin cytoskeleton dynamics was a likely mechanism by which MICAL-1 gene pathogenic variants led to LTE. The seizure onset age was 6-30 years, with most patients experiencing onset at 6-10 years. Affected individuals had auditory auras and some of them had aphasic symptoms. Most patients had FBCTS. EEG revealed temporal or frontotemporal abnormal epileptic activity. Their 1.5-Tesla brain MRI scans were unremarkable. Seizures were well controlled with ASMs such as carbamazepine, methylhydantoin and vigabatrin.
In 2007, a southern Italian family was reported by Colosimo et al[50], in which 13 members over 3 generations had febrile seizures and TLE associated with the SCN1A p.M145T mutation. The SCN1A gene encodes the alpha subunit of the NaV1.1 sodium channel and is highly expressed in the central nervous system. SCN1A gene mutations were associated with a broad spectrum of epilepsy phenotypes and were commonly reported in epilepsies characterized by frequent febrile seizures during childhood; few had been reported in TLE[51]. The SCN1A p.M145T mutation was the first missense mutation found in DIS1 of SCN1A and caused a loss of function of the NaV1.1 channel[52]. All 13 living members had febrile seizures onset from 5 to 45 mo. Nine subjects were affected with only febrile seizures and had normal EEG. Three individuals later developed TLE with epileptiform temporal spikes on EEG, and two of them had HS. The onset age of TLE was 10-13 years. Seizure types included focal seizures with or without awareness and rare nocturnal FBCTS. Seizures in the patient without HS were completely controlled with valproate. Seizures in 1 patient with HS were well controlled with the combination of carbamazepine and primidone. In another patient with HS, seizures continued despite treatment with the combination of topiramate and phenobarbital.
FTLE was always underestimated due to itsheterogeneous intrafamily clinical manifestations. Some family members with subtle symptoms had not received a diagnosis of epilepsy prior to detailed enquiry by a neurologist[11]. Eleven types of FTLE have been identified thus far (Table 1).
In addition to typical temporal lobe seizures, special phenotypes also exist within some types of FTLE, such as migraine and febrile seizures. In 2000, Gambardella et al[53] reported a family with ETL4, in which migraine was a common phenotype among the TLE patients. Chr. 9q21-q22, harboring 604 genes, was correlated with both migraine and ETL4. Understanding of the pathogenetic mechanisms requires the identification of the genes responsible for the phenotype. ETL2, ETL5, ETL6 and ETL11 were associated with a high incidence of febrile seizures, which was also found to be a prominent feature in a number of genetically determined epilepsy cases[54]. Febrile seizures affect approximately 3% of children and increase the risk of developing HS[55]. Moreover, febrile seizures and TLE were associated with common genetic variation, such as the CPA6 and SCN1A genes[36,56]. The prognosis of FTLE with a high incidence of febrile seizures was almost good. However, in some patients with genetically based MTLE-HS and histories of febrile seizures, the prognosis was poor, and the underlying pathogenic genes remain unknown[57]. A growing number of studies had proven that HS and MTLE had polygenic or multifactorial modes of inheritance. The mechanism involves neuron development, differentiation, synaptic signaling, immune response and vascular development, which might provide directions for therapy of MTLE-HS[19].
LTLE was mostly genetic in etiology related to LGI1, RELN, MICAL-1 and DEPDC5 gene mutations. LGI1 and RELN mutations were reported in approximately 35 and 17.5 % of LTLE families respectively[12, 38]. The phenotypes of familial LTLE caused by pathogenic mutations of the LGI1, RELN and MICAL-1 genes were similar. However, the molecular functions of these genes were discrepant, indicating that the mechanism of LTLE was complicated. Notably, some candidate loci were also gradually being recognized, such as the Chr 9q13.11–q13.31 Locus (not mentioned above), which was related to familial LTLE with a higher frequency of febrile seizures and migraine and a lower recurrence of focal to bilateral seizures than ETL1, ETL7 and ETL10[58].
Four gene loci on Chr 12q22-q23.3, 4q13.2-q21.3, 9q21-q22, and 3q25-q26, were closely related to FTLE. These loci each contain 280-604 genes, but the specific pathogenic genes for TLE had not yet been identified. Reports on each type of FTLE were rare, which limits our knowledge and hinders in-depth research. Reaching a complete understanding of the genetics of TLE is still a long-term prospect.
Provenance and peer review: Invited article; Externally peer reviewed.
Peer-review model: Single blind
Corresponding Author's Membership in Professional Societies: Vice president of China Association Against Epilepsy (CAAE), No. 4762.
Specialty type: Neurosciences
Country/Territory of origin: China
Peer-review report’s scientific quality classification
Grade A (Excellent): 0
Grade B (Very good): B
Grade C (Good): C
Grade D (Fair): 0
Grade E (Poor): 0
P-Reviewer: Beran RG, Idiculla PS S-Editor: Wang LL L-Editor: A P-Editor: Wang LL
| 1. | Fisher RS, van Emde Boas W, Blume W, Elger C, Genton P, Lee P, Engel J Jr. Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE). Epilepsia. 2005;46:470-472. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2069] [Cited by in F6Publishing: 1863] [Article Influence: 98.1] [Reference Citation Analysis (0)] |
| 2. | Scheffer IE, Berkovic S, Capovilla G, Connolly MB, French J, Guilhoto L, Hirsch E, Jain S, Mathern GW, Moshé SL, Nordli DR, Perucca E, Tomson T, Wiebe S, Zhang YH, Zuberi SM. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology. Epilepsia. 2017;58:512-521. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2280] [Cited by in F6Publishing: 2743] [Article Influence: 391.9] [Reference Citation Analysis (0)] |
| 3. | Thijs RD, Surges R, O'Brien TJ, Sander JW. Epilepsy in adults. Lancet. 2019;393:689-701. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 662] [Cited by in F6Publishing: 833] [Article Influence: 166.6] [Reference Citation Analysis (0)] |
| 4. | Zhang X, Huang Z, Liu J, Li M, Zhao X, Ye J, Wang Y. Phenotypic and Genotypic Characterization of DEPDC5-Related Familial Focal Epilepsy: Case Series and Literature Review. Front Neurol. 2021;12:641019. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis (0)] |
| 5. | Operto FF, Pastorino GMG, Mazza R, Di Bonaventura C, Marotta R, Pastorino N, Matricardi S, Verrotti A, Carotenuto M, Roccella M. Social cognition and executive functions in children and adolescents with focal epilepsy. Eur J Paediatr Neurol. 2020;28:167-175. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis (0)] |
| 6. | Labate A, Aguglia U, Tripepi G, Mumoli L, Ferlazzo E, Baggetta R, Quattrone A, Gambardella A. Long-term outcome of mild mesial temporal lobe epilepsy: A prospective longitudinal cohort study. Neurology. 2016;86:1904-1910. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 30] [Cited by in F6Publishing: 32] [Article Influence: 4.0] [Reference Citation Analysis (0)] |
| 7. | Roy PL, Ronquillo LH, Ladino LD, Tellez-Zenteno JF. Risk factors associated with drug resistant focal epilepsy in adults: A case control study. Seizure. 2019;73:46-50. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 12] [Cited by in F6Publishing: 19] [Article Influence: 3.8] [Reference Citation Analysis (0)] |
| 8. | Eadie M. Familial temporal lobe epilepsy in the 19th century. Seizure. 2018;54:7-10. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis (0)] |
| 9. | Crichton-Browne J. The Cavendish Lecture: On Dreamy Mental States. Delivered Before the West London Medico-chirurgical Society. Baillière, Tindall and Cox; 1895. [Cited in This Article: ] |
| 10. | Berkovic SF. Familial temporal lobe epilepsy: a new syndrome with adolescent/adult onset and a benign course. Epileptic Seizures and Syndromes. 1994;257-263. [Cited in This Article: ] |
| 11. | Pellinen J, Tafuro E, Yang A, Price D, Friedman D, Holmes M, Barnard S, Detyniecki K, Hegde M, Hixson J, Haut S, Kälviäinen R, French J; Human Epilepsy Project Co-Investigators. Focal nonmotor vs motor seizures: The impact on diagnostic delay in focal epilepsy. Epilepsia. 2020;61:2643-2652. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis (0)] |
| 12. | Ottman R, Winawer MR, Kalachikov S, Barker-Cummings C, Gilliam TC, Pedley TA, Hauser WA. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 2004;62:1120-1126. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 150] [Cited by in F6Publishing: 160] [Article Influence: 8.0] [Reference Citation Analysis (0)] |
| 13. | Kesim YF, Uzun GA, Yucesan E, Tuncer FN, Ozdemir O, Bebek N, Ozbek U, Iseri SA, Baykan B. Screening LGI1 in a cohort of 26 Lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation. Epilepsy Res. 2016;120:73-78. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis (0)] |
| 14. | Bisulli F, Rinaldi C, Pippucci T, Minardi R, Baldassari S, Zenesini C, Mostacci B, Fanella M, Avoni P, Menghi V, Caporali L, Muccioli L, Tinuper P, Licchetta L. Epilepsy with auditory features: Contribution of known genes in 112 patients. Seizure. 2021;85:115-118. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis (0)] |
| 15. | Ayas S, Kurtish SY, Tanrıverdi T, Yeni SN. Evaluation of patients with late-onset and medically refractory temporal lobe epilepsy with mesial temporal sclerosis. Clin Neurol Neurosurg. 2020;198:106209. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis (0)] |
| 16. | Schulz R, Hoppe M, Boesebeck F, Gyimesi C, Pannek HW, Woermann FG, May T, Ebner A. Analysis of reoperation in mesial temporal lobe epilepsy with hippocampal sclerosis. Neurosurgery. 2011;68:89-97; discussion 97. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 1.2] [Reference Citation Analysis (0)] |
| 17. | Andrade-Valença LP, Valença MM, Velasco TR, Carlotti CG Jr, Assirati JA, Galvis-Alonso OY, Neder L, Cendes F, Leite JP. Mesial temporal lobe epilepsy: clinical and neuropathologic findings of familial and sporadic forms. Epilepsia. 2008;49:1046-1054. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 2.0] [Reference Citation Analysis (0)] |
| 18. | Cvetkovska E, Kuzmanovski I, Babunovska M, Boshkovski B, Cangovska TC, Trencevska GK. Phenotypic spectrum in families with mesial temporal lobe epilepsy probands. Seizure. 2018;58:13-16. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis (0)] |
| 19. | Guelfi S, Botia JA, Thom M, Ramasamy A, Perona M, Stanyer L, Martinian L, Trabzuni D, Smith C, Walker R, Ryten M, Reimers M, Weale ME, Hardy J, Matarin M. Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy. Brain. 2019;142:1616-1630. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 7.0] [Reference Citation Analysis (0)] |
| 20. | Ottman R, Risch N, Hauser WA, Pedley TA, Lee JH, Barker-Cummings C, Lustenberger A, Nagle KJ, Lee KS, Scheuer ML. Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet. 1995;10:56-60. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 261] [Cited by in F6Publishing: 274] [Article Influence: 9.4] [Reference Citation Analysis (0)] |
| 21. | Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Boneschi FM, Choi C, Morozov P, Das K, Teplitskaya E, Yu A, Cayanis E, Penchaszadeh G, Kottmann AH, Pedley TA, Hauser WA, Ottman R, Gilliam TC. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nature Genetics. 2002;30:335-341. [Cited in This Article: ] |
| 22. | Yamagata A, Miyazaki Y, Yokoi N, Shigematsu H, Sato Y, Goto-Ito S, Maeda A, Goto T, Sanbo M, Hirabayashi M, Shirouzu M, Fukata Y, Fukata M, Fukai S. Structural basis of epilepsy-related ligand-receptor complex LGI1-ADAM22. Nat Commun. 2018;9:1546. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 32] [Cited by in F6Publishing: 47] [Article Influence: 7.8] [Reference Citation Analysis (0)] |
| 23. | Yamagata A, Fukai S. Insights into the mechanisms of epilepsy from structural biology of LGI1-ADAM22. Cell Mol Life Sci. 2020;77:267-274. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 21] [Cited by in F6Publishing: 22] [Article Influence: 4.4] [Reference Citation Analysis (0)] |
| 24. | Michelucci R, Pasini E, Nobile C. Lateral temporal lobe epilepsies: clinical and genetic features. Epilepsia. 2009;50 Suppl 5:52-54. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 44] [Cited by in F6Publishing: 47] [Article Influence: 3.1] [Reference Citation Analysis (0)] |
| 25. | Dazzo E, Santulli L, Posar A, Fattouch J, Conti S, Lodén-van Straaten M, Mijalkovic J, De Bortoli M, Rosa M, Millino C, Pacchioni B, Di Bonaventura C, Giallonardo AT, Striano S, Striano P, Parmeggiani A, Nobile C. Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras. Epilepsy Res. 2015;110:132-138. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 1.7] [Reference Citation Analysis (0)] |
| 26. | Yokoi N, Fukata Y, Kase D, Miyazaki T, Jaegle M, Ohkawa T, Takahashi N, Iwanari H, Mochizuki Y, Hamakubo T, Imoto K, Meijer D, Watanabe M, Fukata M. Chemical corrector treatment ameliorates increased seizure susceptibility in a mouse model of familial epilepsy. Nat Med. 2015;21:19-26. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 50] [Cited by in F6Publishing: 54] [Article Influence: 5.4] [Reference Citation Analysis (0)] |
| 27. | Depondt C, Van Paesschen W, Matthijs G, Legius E, Martens K, Demaerel P, Wilms G. Familial temporal lobe epilepsy with febrile seizures. Neurology. 2002;58:1429-1433. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 33] [Cited by in F6Publishing: 34] [Article Influence: 1.5] [Reference Citation Analysis (0)] |
| 28. | Claes L, Audenaert D, Deprez L, Van Paesschen W, Depondt C, Goossens D, Del-Favero J, Van Broeckhoven C, De Jonghe P. Novel locus on chromosome 12q22-q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures. J Med Genet. 2004;41:710-714. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 46] [Cited by in F6Publishing: 48] [Article Influence: 2.5] [Reference Citation Analysis (0)] |
| 29. | Gurnett CA, Dobbs MB, Keppel CR, Pincus ER, Jansen LA, Bowcock AM. Additional evidence of a locus for complex febrile and afebrile seizures on chromosome 12q22-23.3. Neurogenetics. 2007;8:61-63. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 0.4] [Reference Citation Analysis (0)] |
| 30. | Vari MS, Traverso M, Bellini T, Madia F, Pinto F, Minetti C, Striano P, Zara F. De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy. Seizure. 2017;50:80-82. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis (0)] |
| 31. | Wei Z, Liu C, Wu Z, Cao M, Qiao X, Han T, Zhang Y, Liu Y, Deng Y. The prognosis of epilepsy patients with CACNA1H missense variants: A longitudinal cohort study. Seizure. 2021;91:52-59. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis (0)] |
| 32. | Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3. Neurology. 2007;68:2107-2112. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 52] [Cited by in F6Publishing: 52] [Article Influence: 3.1] [Reference Citation Analysis (0)] |
| 33. | Teive HA, Piovesan EJ, Kowacs PA, Werneck LC. Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q new evidence for a genetic link between epilepsy and migraine. Neurology. 2008;70:896; author reply 896-896; author reply 897. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis (0)] |
| 34. | Nye BL, Thadani VM. Migraine and epilepsy: review of the literature. Headache. 2015;55:359-380. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 66] [Cited by in F6Publishing: 74] [Article Influence: 8.2] [Reference Citation Analysis (0)] |
| 35. | Tikka-Kleemola P, Artto V, Vepsäläinen S, Sobel EM, Räty S, Kaunisto MA, Anttila V, Hämäläinen E, Sumelahti ML, Ilmavirta M, Färkkilä M, Kallela M, Palotie A, Wessman M. A visual migraine aura locus maps to 9q21-q22. Neurology. 2010;74:1171-1177. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 1.2] [Reference Citation Analysis (0)] |
| 36. | Salzmann A, Guipponi M, Lyons PJ, Fricker LD, Sapio M, Lambercy C, Buresi C, Ouled Amar Bencheikh B, Lahjouji F, Ouazzani R, Crespel A, Chaigne D, Malafosse A. Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy. Hum Mutat. 2012;33:124-135. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 28] [Cited by in F6Publishing: 30] [Article Influence: 2.3] [Reference Citation Analysis (0)] |
| 37. | Chahine L, Abou-Khalil B, Siren A, Andermann F, Hedera P, Ge Q, Andermann E, Pandolfo M. A new locus for familial temporal lobe epilepsy on chromosome 3q. Epilepsy Res. 2013;106:338-344. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 1.4] [Reference Citation Analysis (0)] |
| 38. | Dazzo E, Fanciulli M, Serioli E, Minervini G, Pulitano P, Binelli S, Di Bonaventura C, Luisi C, Pasini E, Striano S, Striano P, Coppola G, Chiavegato A, Radovic S, Spadotto A, Uzzau S, La Neve A, Giallonardo AT, Mecarelli O, Tosatto SC, Ottman R, Michelucci R, Nobile C. Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. Am J Hum Genet. 2015;96:992-1000. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 73] [Cited by in F6Publishing: 76] [Article Influence: 8.4] [Reference Citation Analysis (0)] |
| 39. | Faini G, Del Bene F, Albadri S. Reelin functions beyond neuronal migration: from synaptogenesis to network activity modulation. Curr Opin Neurobiol. 2021;66:135-143. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 9] [Cited by in F6Publishing: 18] [Article Influence: 4.5] [Reference Citation Analysis (0)] |
| 40. | Michelucci R, Pulitano P, Di Bonaventura C, Binelli S, Luisi C, Pasini E, Striano S, Striano P, Coppola G, La Neve A, Giallonardo AT, Mecarelli O, Serioli E, Dazzo E, Fanciulli M, Nobile C. The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations. Epilepsy Behav. 2017;68:103-107. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 28] [Cited by in F6Publishing: 27] [Article Influence: 3.9] [Reference Citation Analysis (0)] |
| 41. | Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat Genet. 2000;26:93-96. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 646] [Cited by in F6Publishing: 567] [Article Influence: 23.6] [Reference Citation Analysis (0)] |
| 42. | Zaki M, Shehab M, El-Aleem AA, Abdel-Salam G, Koeller HB, Ilkin Y, Ross ME, Dobyns WB, Gleeson JG. Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation. Am J Med Genet A. 2007;143A:939-944. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 60] [Cited by in F6Publishing: 63] [Article Influence: 3.7] [Reference Citation Analysis (0)] |
| 43. | Guipponi M, Chentouf A, Webling KE, Freimann K, Crespel A, Nobile C, Lemke JR, Hansen J, Dorn T, Lesca G, Ryvlin P, Hirsch E, Rudolf G, Rosenberg DS, Weber Y, Becker F, Helbig I, Muhle H, Salzmann A, Chaouch M, Oubaiche ML, Ziglio S, Gehrig C, Santoni F, Pizzato M, Langel Ü, Antonarakis SE. Galanin pathogenic mutations in temporal lobe epilepsy. Hum Mol Genet. 2015;24:3082-3091. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 2.3] [Reference Citation Analysis (0)] |
| 44. | Ishida S, Picard F, Rudolf G, Noé E, Achaz G, Thomas P, Genton P, Mundwiller E, Wolff M, Marescaux C, Miles R, Baulac M, Hirsch E, Leguern E, Baulac S. Mutations of DEPDC5 cause autosomal dominant focal epilepsies. Nat Genet. 2013;45:552-555. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 174] [Cited by in F6Publishing: 168] [Article Influence: 15.3] [Reference Citation Analysis (0)] |
| 45. | Picard F, Baulac S, Kahane P, Hirsch E, Sebastianelli R, Thomas P, Vigevano F, Genton P, Guerrini R, Gericke CA, An I, Rudolf G, Herman A, Brice A, Marescaux C, LeGuern E. Dominant partial epilepsies. A clinical, electrophysiological and genetic study of 19 European families. Brain. 2000;123 ( Pt 6):1247-1262. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 60] [Cited by in F6Publishing: 62] [Article Influence: 2.6] [Reference Citation Analysis (0)] |
| 46. | Striano P, Serioli E, Santulli L, Manna I, Labate A, Dazzo E, Pasini E, Gambardella A, Michelucci R, Striano S, Nobile C. DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy. Epilepsia. 2015;56:e168-e171. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 2.8] [Reference Citation Analysis (0)] |
| 47. | Pippucci T, Licchetta L, Baldassari S, Palombo F, Menghi V, D'Aurizio R, Leta C, Stipa C, Boero G, d'Orsi G, Magi A, Scheffer I, Seri M, Tinuper P, Bisulli F. Epilepsy with auditory features: A heterogeneous clinico-molecular disease. Neurol Genet. 2015;1:e5. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 40] [Cited by in F6Publishing: 41] [Article Influence: 4.6] [Reference Citation Analysis (0)] |
| 48. | Dazzo E, Rehberg K, Michelucci R, Passarelli D, Boniver C, Vianello Dri V, Striano P, Striano S, Pasterkamp RJ, Nobile C. Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy. Ann Neurol. 2018;83:483-493. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 3.3] [Reference Citation Analysis (0)] |
| 49. | Luo J, Xu Y, Zhu Q, Zhao F, Zhang Y, Peng X, Wang W, Wang X. Expression pattern of Mical-1 in the temporal neocortex of patients with intractable temporal epilepsy and pilocarpine-induced rat model. Synapse. 2011;65:1213-1221. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 1.2] [Reference Citation Analysis (0)] |
| 50. | Colosimo E, Gambardella A, Mantegazza M, Labate A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, Quattrone A. Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation. Epilepsia. 2007;48:1691-1696. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 36] [Cited by in F6Publishing: 37] [Article Influence: 2.2] [Reference Citation Analysis (0)] |
| 51. | Scheffer IE, Nabbout R. SCN1A-related phenotypes: Epilepsy and beyond. Epilepsia. 2019;60 Suppl 3:S17-S24. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 49] [Cited by in F6Publishing: 60] [Article Influence: 12.0] [Reference Citation Analysis (0)] |
| 52. | Mantegazza M, Gambardella A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Labate A, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, Quattrone A. Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures. Proc Natl Acad Sci U S A. 2005;102:18177-18182. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 147] [Cited by in F6Publishing: 143] [Article Influence: 7.5] [Reference Citation Analysis (0)] |
| 53. | Gambardella A, Messina D, Le Piane E, Oliveri RL, Annesi G, Zappia M, Andermann E, Quattrone A, Aguglia U. Familial temporal lobe epilepsy autosomal dominant inheritance in a large pedigree from southern Italy. Epilepsy Res. 2000;38:127-132. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 42] [Cited by in F6Publishing: 44] [Article Influence: 1.8] [Reference Citation Analysis (0)] |
| 54. | Kasperaviciute D, Catarino CB, Matarin M, Leu C, Novy J, Tostevin A, Leal B, Hessel EV, Hallmann K, Hildebrand MS, Dahl HH, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty CP, Dorn T, Hansen J, Krämer G, Steinhoff BJ, Zumsteg D, Duncan S, Kälviäinen RK, Eriksson KJ, Kantanen AM, Pandolfo M, Gruber-Sedlmayr U, Schlachter K, Reinthaler EM, Stogmann E, Zimprich F, Théâtre E, Smith C, O'Brien TJ, Meng Tan K, Petrovski S, Robbiano A, Paravidino R, Zara F, Striano P, Sperling MR, Buono RJ, Hakonarson H, Chaves J, Costa PP, Silva BM, da Silva AM, de Graan PN, Koeleman BP, Becker A, Schoch S, von Lehe M, Reif PS, Rosenow F, Becker F, Weber Y, Lerche H, Rössler K, Buchfelder M, Hamer HM, Kobow K, Coras R, Blumcke I, Scheffer IE, Berkovic SF, Weale ME; UK Brain Expression Consortium, Delanty N, Depondt C, Cavalleri GL, Kunz WS, Sisodiya SM. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Brain. 2013;136:3140-3150. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 135] [Cited by in F6Publishing: 120] [Article Influence: 10.9] [Reference Citation Analysis (0)] |
| 55. | Moreira-Filho CA, Bando SY, Bertonha FB, Iamashita P, Silva FN, Costa Lda F, Silva AV, Castro LH, Wen HT. Community structure analysis of transcriptional networks reveals distinct molecular pathways for early- and late-onset temporal lobe epilepsy with childhood febrile seizures. PLoS One. 2015;10:e0128174. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 1.3] [Reference Citation Analysis (0)] |
| 56. | Perucca P, Scheffer IE, Harvey AS, James PA, Lunke S, Thorne N, Gaff C, Regan BM, Damiano JA, Hildebrand MS, Berkovic SF, O'Brien TJ, Kwan P. Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsy. Epilepsy Res. 2017;131:1-8. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 61] [Cited by in F6Publishing: 58] [Article Influence: 8.3] [Reference Citation Analysis (0)] |
| 57. | Jobst BC. It Goes Downhill From Here but Do Not Despair: Mesial Temporal Lobe Epilepsy Is a Progressive Disease, but It Can Be Benign. Epilepsy Curr. 2016;16:380-381. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis (0)] |
| 58. | Bisulli F, Naldi I, Baldassari S, Magini P, Licchetta L, Castegnaro G, Fabbri M, Stipa C, Ferrari S, Seri M, Gonçalves Silva GE, Tinuper P, Pippucci T. Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31. Epilepsia. 2014;55:841-848. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 0.9] [Reference Citation Analysis (0)] |