[1]
|
Bingaman, W.E. (2004) Surgery for Focal Cortical Dysplasia. Neurology, 62, S30-S34.
https://doi.org/10.1212/01.WNL.0000114508.31261.E6
|
[2]
|
Wong, M. (2008) Mechanisms of Epileptogenesis in Tuberous Sclerosis Complex and Related Malformations of Cortical Development with Abnormal Glioneuronal Prolifer-ation. Epilepsia, 49, 8-21.
https://doi.org/10.1111/j.1528-1167.2007.01270.x
|
[3]
|
Palmini, A., Najm, I., Avanzini, G., et al. (2004) Termi-nology and Classification of the Cortical Dysplasias. Neurology, 62, S2-S8. https://doi.org/10.1212/01.WNL.0000114507.30388.7E
|
[4]
|
Ingmar Blümcke, Maria Thom, Eleonora Aronica, 等. 局灶性皮层发育不良的临床病理分类新标准——ILAE诊断方法委员会协作组专家共识[J]. 癫痫杂志, 2020, 6(6): 537-545.
|
[5]
|
Kobow, K., Ziemann, M., Kaipananickal, H., et al. (2019) Genomic DNA Methylation Distinguishes Subtypes of Human Focal Cortical Dysplasia. Epilepsia, 60, 1091-1103. https://doi.org/10.1111/epi.14934
|
[6]
|
Krsek, P., Jahodova, A., Maton, B., et al. (2010) Low-Grade Focal Cortical Dysplasia Is Associated with Prenatal and Perinatal Brain Injury. Epilepsia, 51, 2440-2448. https://doi.org/10.1111/j.1528-1167.2010.02730.x
|
[7]
|
Chen, J., Tsai, V., Parker, W.E., et al. (2013) Detection of Human Papillomavirus in Human Focal Cortical Dysplasia Type IIB. Annals of Neurology, 72, 881-892. https://doi.org/10.1002/ana.23795
|
[8]
|
Baldassari, S., Ribierre, T., Marsan, E., et al. (2019) Dissecting the Genetic Basis of Focal Cortical Dysplasia: A Large Cohort Study. Acta Neuropathologica, 138, 885-900. https://doi.org/10.1007/s00401-019-02061-5
|
[9]
|
Guerrini, R., Cavallin, M., Pippucci, T., et al. (2021) Is Focal Cortical Dysplasia/Epilepsy Caused by Somatic MTOR Mutations Always a Unilateral Disorder? Neurology Genetics, 7, e540.
https://doi.org/10.1212/NXG.0000000000000540
|
[10]
|
Jesus-Ribeiro, J., Pires, L.M., Melo, J.D., et al. (2021) Genomic and Epigenetic Advances in Focal Cortical Dysplasia Types I and II: A Scoping Review. Frontiers in Neuro-science, 14, Article ID: 580357.
https://doi.org/10.3389/fnins.2020.580357
|
[11]
|
Jansen, L.A., Mirzaa, G.M., Ishak, G.E., et al. (2015) PI3K/AKT Pathway Mutations Cause a Spectrum of Brain Malformations from Megalencephaly to Focal Cortical Dysplasia. Brain, 138, 1613-1628.
https://doi.org/10.1093/brain/awv045
|
[12]
|
Greig, L.C., Woodworth, M.B., Galazo, M.J., et al. (2013) Molecular Logic of Neocortical Projection Neuron Specification, Development and Diversity. Nature Reviews Neuroscience, 14, 755-769. https://doi.org/10.1038/nrn3586
|
[13]
|
Vecchi, M., Barba, C., De Carlo, D., et al. (2016) Symptomatic and Presumed Symptomatic Focal Epilepsies in Childhood: An Observational, Prospective Multicentre Study. Epilepsia, 57, 1808-1816.
https://doi.org/10.1111/epi.13574
|
[14]
|
Bast, T., Ramantani, G., Seitz, A., et al. (2006) Focal Cortical Dysplasia: Prevalence, Clinical Presentation and Epilepsy in Children and Adults. Acta Neurologica Scandinavica, 113, 72-81.
https://doi.org/10.1111/j.1600-0404.2005.00555.x
|
[15]
|
Fauser, S., Strobl, H., Pantazis, G., et al. (2006) Clinical Characteristics in Focal Cortical Dysplasia: A Retrospective Evaluation in a Series of 120 Patients. Brain: A Journal of Neurology, 129, 1907. https://doi.org/10.1093/brain/awl133
|
[16]
|
Wiwattanadittakul, N., Suwannachote, S., You, X., et al. (2021) Spatiotemporal Distribution and Age of Seizure Onset in a Pediatric Epilepsy Surgery Cohort with Cor-tical Dysplasia. Epilepsy Research, 172, Article ID: 106598.
https://doi.org/10.1016/j.eplepsyres.2021.106598
|
[17]
|
Lamberink, H.J., Otte, W.M., Blümcke, I., et al. (2020) Seizure Outcome and Use of Antiepileptic Drugs after Epilepsy Surgery According to Histopathological Diagnosis: A Retrospective Multicentre Cohort Study. The Lancet Neurology, 19, 748-757. https://doi.org/10.1016/S1474-4422(20)30220-9
|
[18]
|
Lawson, J.A., Birchansky, S., Pacheco, E., et al. (2005) Dis-tinct Clinicopathologic Subtypes of Cortical Dysplasia of Taylor. Neurology, 64, 55. https://doi.org/10.1212/01.WNL.0000148647.55705.A3
|
[19]
|
Giacomo, R.D., Martin, R., Mai, R., et al. (2019) Stereo-EEG Ictal/Interictal Patterns and Underlying Pathologies. Seizure, 72, 54-60. https://doi.org/10.1016/j.seizure.2019.10.001
|
[20]
|
Kerber, L., et al. (2013) High Frequency Oscillations Mirror Disease Activity in Patients with Focal Cortical Dysplasia. Epilepsia: Journal of the International League against Epi-lepsy, 54, 1428-1436. https://doi.org/10.1111/epi.12262
|
[21]
|
Barba, C. (2021) Focal Cortical Dysplasia: An Update on Diagnosis and Treatment. Expert Review of Neurotherapeutics, 21, 1213-1224.
|
[22]
|
郭韬, 刘倩薇, 武江, 等. 脑磁图联合神经导航手术治疗局灶性皮层发育不良所致额颞癫痫[J]. 实用医学杂志, 2018, 34(9): 1416-1419.
|
[23]
|
Chassoux, F., Rodrigo, S., Semah, F., et al. (2010) FDG-PET Improves Surgical Outcome in Negative MRI Taylor-Type Focal Cortical Dysplasias. Neurology, 75, 2168-2175. https://doi.org/10.1212/WNL.0b013e31820203a9
|
[24]
|
Wang, I., Oh, S., Blümcke, I., et al. (2020) Value of 7T MRI and Post-Processing in Patients with Nonlesional 3T MRI Undergoing Epilepsy Presurgical Evaluation. Epilepsia, 61, 2509-2520. https://doi.org/10.1111/epi.16682
|
[25]
|
Tahry, R.E., Santos, S.F., Vrielynck, P., et al. (2020) Addi-tional Clinical Value of Voxel-Based Morphometric MRI Post-Processing for MRI-Negative Epilepsies: A Prospective Study. Epileptic Disorders, 22, 156-164.
https://doi.org/10.1684/epd.2020.1152
|
[26]
|
陈龙, 冯兆海, 姜磊, 等. MRI阴性药物难治性颞叶癫痫的外科治疗[J]. 新疆医学, 2020, 50(6): 552-555.
|
[27]
|
Bourdillon, P., Rheims, S., Catenoix, H., et al. (2019) Malformations of Cortical Development: New Surgical Advances. Revue Neurologique, 175, 183-188. https://doi.org/10.1016/j.neurol.2019.01.392
|
[28]
|
Cobourn, K., Fayed, I., Keating, R.F., et al. (2018) Early Out-comes of Stereoelectroencephalography Followed by MR-Guided Laser Interstitial Thermal Therapy: A Paradigm for Minimally Invasive Epilepsy Surgery. Neurosurgical Focus, 45, E8. https://doi.org/10.3171/2018.6.FOCUS18209
|
[29]
|
French, J.A., Lawson, J.A., Yapici, Z., et al. (2016) Adjunctive Everolimus Therapy for Treatment-Resistant Focal-Onset Seizures Associated with Tuberous Sclerosis (EXIST-3): A Phase 3, Randomised, Double-Blind, Placebo-Controlled Study. The Lancet, 388, 2153-2163. https://doi.org/10.1016/S0140-6736(16)31419-2
|