Curatolo P, Moavero R, de Vries PJ. Neurological and neuropsychiatric aspects of tuberous sclerosis complex[J]. Lancet Neurol, 2015, 14(7):733-745.
[2]
Yang G, Shi ZN, Meng Y, et al. Phenotypic and genotypic characterization of Chinese children diagnosed with tuberous sclerosis complex[J]. Clin Genet, 2017, 91(5):764-768.
[3]
Wong M. Mammalian target of rapamycin (mTOR) pathways in neurological diseases[J]. Biomed J, 2013, 36(2):40-50.
[4]
Overwater IE, Bindels-de Heus K, Rietman AB, et al. Epilepsy in children with tuberous sclerosis complex:chance of remission and response to antiepileptic drugs[J]. Epilepsia, 2015, 56(8):1239-1245.
[5]
Cui J, Yu X, Liang S, et al. First five generations Chinese family of tuberous scleroses complex due to a new mutation of the TSC1 gene[J]. J Clin Neurosci, 2018, 54:39-44.
[6]
Kothare SV, Singh K, Chalifoux JR, et al. Severity of manifestations in tuberous sclerosis complex in relation to genotype[J]. Epilepsia, 2014, 55(7):1025-1029.
[7]
Northrup H, Krueger DA; International Tuberous Sclerosis Complex Consensus Group. Tuberous sclerosis complex diagnostic criteria update:recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference[J]. Pediatr Neurol, 2013, 49(4):243-254.
[8]
Wong M. A critical review of mTOR inhibitors and epilepsy:from basic science to clinical trials[J]. Expert Rev Neurother, 2013, 13(6):657-669.
[9]
Yang G, Yang L, Yang X, et al. Efficacy and safety of a mammalian target of rapamycin inhibitor in pediatric patients with tuberous sclerosis complex:a systematic review and meta-analysis[J]. Exp Ther Med, 2015, 9(2):626-630.
[10]
Samueli S, Abraham K, Dressler A, et al. Efficacy and safety of Everolimus in children with TSC-associated epilepsy-pilot data from an open single-center prospective study[J]. Orphanet J Rare Dis, 2016, 11(1):145.
[11]
Krueger DA, Wilfong AA, Mays M, et al. Long-term treatment of epilepsy with everolimus in tuberous sclerosis[J]. Neurology, 2016, 87(23):2408-2415.
Canpolat M, Per H, Gumus H, et al. Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex:results of 7 children from a cohort of 86[J]. Childs Nerv Syst, 2014, 30(2):227-240.
[14]
Zou LP, Liu YT. Letter re:Sirolimus for epilepsy in children with tuberous sclerosis complex:A randomized controlled trial[J]. Neurology, 2017, 88(10):1008.
[15]
Curatolo P, Nabbout R, Lagae L, et al. Management of epilepsy associated with tuberous sclerosis complex:updated clinical recommendations[J]. Eur J Paediatr Neurol, 2018, 22(5):738-748.
Park S, Lee EJ, Eom S, et al. Ketogenic diet for the management of epilepsy associated with tuberous sclerosis complex in children[J]. J Epilepsy Res, 2017, 7(1):45-49.
[18]
Ruppe V, Dilsiz P, Reiss CS, et al. Developmental brain abnormalities in tuberous sclerosis complex:a comparative tissue analysis of cortical tubers and perituberal cortex[J]. Epilepsia, 2014, 55(4):539-550.
[19]
Liang S, Zhang J, Yang Z, et al. Long-term outcomes of epilepsy surgery in tuberous sclerosis complex[J]. J Neurol, 2017, 264(6):1146-1154.
[20]
Arya R, Tenney JR, Horn PS, et al. Long-term outcomes of resective epilepsy surgery after invasive presurgical evaluation in children with tuberous sclerosis complex and bilateral multiple lesions[J]. J Neurosurg Pediatr, 2015, 15(1):26-33.
[21]
Rovira À, Ruiz-Falcó ML, García-Esparza E, et al. Recommendations for the radiological diagnosis and follow-up of neuropathological abnormalities associated with tuberous sclerosis complex[J]. J Neurooncol, 2014, 118(2):205-223.
[22]
Jahodova A, Krsek P, Kyncl M, et al. Distinctive MRI features of the epileptogenic zone in children with tuberous sclerosis[J]. Eur J Radiol, 2014, 83(4):703-709.
[23]
Sun K, Cui J, Wang B, et al. Magnetic resonance imaging of tuberous sclerosis complex with or without epilepsy at 7T[J]. Neuroradiology, 2018, 60(8):785-794.
[24]
Zhang MN, Zou LP, Wang YY, et al. Calcification in cerebral parenchyma affects pharmacoresistant epilepsy in tuberous sclerosis[J]. Seizure, 2018, 60:86-90.
[25]
Yogi A, Hirata Y, Karavaeva E, et al. DTI of tuber and perituberal tissue can predict epileptogenicity in tuberous sclerosis complex[J]. Neurology, 2015, 85(23):2011-2015.
[26]
Song P, Joo EY, Seo DW, et al. Seizure localization in patients with multiple tubers:presurgical evaluation in tuberous sclerosis[J]. J Epilepsy Res, 2012, 2(1):16-20.
[27]
Chandra PS, Salamon N, Huang J, et al. FDG-PET/MRI coregistration and diffusion-tensor imaging distinguish epileptogenic tubers and cortex in patients with tuberous sclerosis complex:a preliminary report[J]. Epilepsia, 2006, 47(9):1543-1549.
[28]
Chugani HT, Luat AF, Kumar A, et al. α-[11C]-Methyl-L-tryptophan-PET in 191 patients with tuberous sclerosis complex[J]. Neurology, 2013, 81(7):674-680.
[29]
Fallah A, Guyatt GH, Snead OC 3rd, et al. Predictors of seizure outcomes in children with tuberous sclerosis complex and intractable epilepsy undergoing resective epilepsy surgery:an individual participant data meta-analysis[J]. PLoS One, 2013, 8(2):e53565.
[30]
Leal AJ, Dias AI, Vieira JP, et al. Analysis of the dynamics and origin of epileptic activity in patients with tuberous sclerosis evaluated for surgery of epilepsy[J]. Clin Neurophysiol, 2008, 119(4):853-861.
[31]
Okanishi T, Akiyama T, Mayo E, et al. Magnetoencephalography spike sources interrelate the extensive epileptogenic zone of tuberous sclerosis complex[J]. Epilepsy Res, 2016, 127:302-310.
[32]
Liang S, Li A, Zhao M, et al. Epilepsy surgery in tuberous sclerosis complex:emphasis on surgical candidate and neuropsychology[J]. Epilepsia, 2010, 51(11):2316-2321.
[33]
Hsieh DT, Whiteway SL, Rohena LO, et al. Tuberous sclerosis complex:five new things[J]. Neurol Clin Pract, 2016, 6(4):339-347.
[34]
van Eeghen AM, Chu-Shore CJ, Pulsifer MB, et al. Cognitive and adaptive development of patients with tuberous sclerosis complex:a retrospective, longitudinal investigation[J]. Epilepsy Behav, 2012, 23(1):10-15.
[35]
Jansen FE, van Huffelen AC, Bourez-Swart M, et al. Consistent localization of interictal epileptiform activity on EEGs of patients with tuberous sclerosis complex[J]. Epilepsia, 2005, 46(3):415-419.
[36]
Liang S, Wang S, Zhang J, et al. Long-term outcomes of epilepsy surgery in school-aged children with partial epilepsy[J]. Pediatr Neurol, 2012, 47(4):284-290.
[37]
Shahid A. Resecting the epileptogenic tuber:what happens in the long term?[J]. Epilepsia, 2013, 54(Suppl 9):135-138.
[38]
Jansen FE, van Huffelen AC, Algra A, et al. Epilepsy surgery in tuberous sclerosis:a systematic review[J]. Epilepsia, 2007, 48(8):1477-1484.
[39]
Zhang K, Hu WH, Zhang C, et al. Predictors of seizure freedom after surgical management of tuberous sclerosis complex:a systematic review and meta analysis[J]. Epilepsy Res, 2013, 105(3):377-383.
[40]
Kannan L, Vogrin S, Bailey C, et al. Centre of epileptogenic tubers generate and propagate seizures in tuberous sclerosis[J]. Brain, 2016, 139(Pt 10):2653-2667.
[41]
Wu JY, Salamon N, Kirsch HE, et al. Noninvasive testing, early surgery, and seizure freedom in tuberous sclerosis complex[J]. Neurology, 2010, 74(5):392-398.
[42]
Roulet-Perez E, Davidoff V, Mayor-Dubois C, et al. Impact of severe epilepsy on development:recovery potential after successful early epilepsy surgery[J]. Epilepsia, 2010, 51(7):1266-1276.
[43]
Jiang T, Du J, Raynald, et al. Presurgical administration of mTOR inhibitors in patients with large subependymal giant cell astrocytoma associated with tuberous sclerosis complex[J]. World Neurosurg, 2017, 107:1053.e1-1053.e6.
[44]
Carlson C, Teutonico F, Elliott RE, et al. Bilateral invasive electroencephalography in patients with tuberous sclerosis complex:a path to surgery?[J]. J Neurosurg Pediatr, 2011, 7(4):421-430.
[45]
Liu SY, An N, Yang MH, et al. Surgical treatment for epilepsy in 17 children with tuberous sclerosis-related West syndrome[J]. Epilepsy Res, 2012, 101(1-2):36-45.
Shenkman Z, Rockoff MA, Eldredge EA, et al. Anaesthetic management of children with tuberous sclerosis[J]. Paediatr Anaesth, 2002, 12(8):700-704.
[48]
Okanishi T, Akiyama T, Tanaka S, et al. Interictal high frequency oscillations correlating with seizure outcome in patients with widespread epileptic networks in tuberous sclerosis complex[J]. Epilepsia, 2014, 55(10):1602-1610.
[49]
Fujiwara H, Leach JL, Greiner HM, et al. Resection of ictal high frequency oscillations is associated with favorable surgical outcome in pediatric drug resistant epilepsy secondary to tuberous sclerosis complex[J]. Epilepsy Res, 2016, 126:90-97.
[50]
Ma TS, Elliott RE, Ruppe V, et al. Electrocorticographic evidence of perituberal cortex epileptogenicity in tuberous sclerosis complex[J]. J Neurosurg Pediatr, 2012, 10(5):376-382.
[51]
Krsek P, Jahodova A, Kyncl M, et al. Predictors of seizure-free outcome after epilepsy surgery for pediatric tuberous sclerosis complex[J]. Epilepsia, 2013, 54(11):1913-1921.
[52]
Dogan MS, Gumus K, Koc G, et al. Brain diffusion tensor imaging in children with tuberous sclerosis[J]. Diagn Interv Imaging, 2016, 97(2):171-176.
[53]
Asano E, Benedek K, Shah A, et al. Is intraoperative electrocorticography reliable in children with intractable neocortical epilepsy?[J]. Epilepsia, 2004, 45(9):1091-1099.
[54]
Oh S, Stewart T, Miller I, et al. In vivo optical properties of cortical tubers in children with tuberous sclerosis complex (TSC):a preliminary investigation[J]. Epilepsia, 2011, 52(9):1699-1704.
[55]
Colicchio G, Montano N, Fuggetta F, et al. Vagus nerve stimulation in drug-resistant epilepsies. Analysis of potential prognostic factors in a cohort of patients with long-term follow-up[J]. Acta Neurochir (Wien), 2012, 154(12):2237-2240.
[56]
Englot DJ, Chang EF, Auguste KI. Vagus nerve stimulation for epilepsy:a meta-analysis of efficacy and predictors of response[J]. J Neurosurg, 2011, 115(6):1248-1255.
[57]
Fallah A, Weil AG, Wang S, et al. Cost-utility analysis of competing treatment strategies for drug-resistant epilepsy in children with tuberous sclerosis complex[J]. Epilepsy Behav, 2016, 63:79-88.
[58]
Tovar-Spinoza Z, Ziechmann R, Zyck S. Single and staged laser interstitial thermal therapy ablation for cortical tubers causing refractory epilepsy in pediatric patients[J]. Neurosurg Focus, 2018, 45(3):E9.
Liang S, Zhang S, Hu X, et al. Anterior corpus callosotomy in school-aged children with Lennox-Gastaut syndrome:a prospective study[J]. Eur J Paediatr Neurol, 2014, 18(6):670-676.
[62]
Liang S, Li A, Jiang H, et al. Anterior corpus callosotomy in patients with intractable generalized epilepsy and mental retardation[J]. Stereotact Funct Neurosurg, 2010, 88(4):246-252.