1. Armstrong DD. The neuropathology of temporal lobe epilepsy. J Neuropathol Exp Neurol 1993; 52: 433-443.
2.
Barba C, Blumcke I, Winawer MR, Hartlieb T, Kang HC, Grisotto L, Chipaux M, Bien CG, Heřmanovská B, Porter BE, Lidov HGV, Cetica V, Woermann FG, Lopez-Rivera JA, Canoll PD, Mader I, D’Incerti L, Baldassari S, Yang E, Gaballa A, Vogel H, Straka B, Macconi L, Polster T, Grant GA, Krsková L, Shin HJ, Ko A, Crino PB, Krsek P, Lee JH, Lal D, Baulac S, Poduri A, Guerrini R; SLC35A2 Study Group. Clinical features, neuropathology, and surgical outcome in patients with refractory epilepsy and brain somatic variants in the SLC35A2 gene. Neurology 2023; 100: e528-e542.
3.
Blumcke I, Coras R, Busch RM, Morita-Sherman M, Lal D, Prayson R, Cendes F, Lopes-Cendes I, Rogerio F, Almeida VS, Rocha CS, Suk Sim N, Lee JH, Kim SH, Baulac S, Baldassari S, Adle-Biassette H, Walsh CA, Bizzotto S, Doan RN, Morillo KS, Aronica E, Mühlebner A, Becker A, Cienfuegos J, Garbelli R, Giannini C, Honavar M, Jacques TS, Thom M, Mahadevan A, Miyata H, Niehusmann P, Sarnat HB, Söylemezoglu F, Najm I. Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial. Epilepsia 2021; 62: 1416-1428.
4.
Bonduelle T, Hartlieb T, Baldassari S, Sim NS, Kim SH, Kang HC, Kobow K, Coras R, Chipaux M, Dorfmüller G, Adle-Biassette H, Aronica E, Lee JH, Blumcke I, Baulac S. Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE). Acta Neuropathol Commun 2021; 9: 3.
5.
Chun JJ, Shatz CJ. Interstitial cells of the adult neocortical white matter are the remnant of the early generated suplate neuron population. J Comp Neurol 1989; 282: 555-569.
6.
Donati D, Akhyani N, Foghell-Hahn A, Cermelli C, CassianiIngoni R, Vortmeyer A, Heiss JD, Cogen P, Gaillard WD, Sato S, Theodore WH, Jacobson S. Detection of human herpesvirus-6 in mesial temporal lobe epilepsy surgical brain resections. Neurology 2003; 61: 1405-1411.
7.
Gaballa A, Woermann FG, Cloppenborg T, Kalbhenn T, Blümcke I, Bien CG, Fauser S. Clinical characteristics and postoperative seizure outcome in patients with mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy. Epilepsy 2021; 62: 2920-2931.
8.
Garganis K, Kokkinos V, Zountsas B, Dinopoulos A, Coras R, Blümcke I. Temporal lobe “plus” epilepsy associated with oligodendroglial hyperplasia (MOGHE). Acta Neurol Scand 2019; 140: 296-300.
9.
Hardiman O, Burke T, Phillips J, Murphy S, O’Moore B, Staunton H, Farrell MA. Microdysgenesis in resected temporal neocortex: incidence and clinical significance in focal epilepsy. Neurology 1988; 38: 1041-1047.
10.
Hartlieb T, Pieper T, Holthausen H, Kluger G, Blumke I, Coras R, Kobow K, Persits S, Kudernatsch M. Treatment options in patients with MOGHE (mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy). Conference: 14th International Epilepsy Colloquin Lausanne. September 2022.
11.
Hartlieb T, Winker P, Coras R, Pieper T, Holthausen H, Blümcke I, Staudt M, Kudernatsch M. Age-related MR characteristics in mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE). Epilepsy Behav 2019; 91: 68-74.
12.
Mendes Coelho VC, Morita-Sherman M, Yasuda CL, Alvim MMK, Juarez Amorim B, Tedeschi H, Ghizoni E, Rogerio F, Cendes F. Magnetic resonance imaging findings and clinical characteristics in mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy in a predominantly adult cohort. Epilepsia 2021; 62: 1429-1441.
13.
Najm I, Lal D, Vanegas MA, Cendes F, Lopes-Cendes I, Palmini A, Paglioli E, Sarnat HB, Walsh CA, Wiebe S, Aronica E, Baulac S, Coras R, Kobow K, Cross JH, Garbelli R, Holthausen H, Rössler K, Thom M, El-Osta A, Lee JH, Miyata H, Guerrini R, Piao YS, Zhou D, Blümcke I. The ILAE consensus classification of focal cortical dysplasia (FCD): an update proposed by a hoc Task Force of ILAE Diagnostic Methods commission. Epilepsia 2022; 63: 1899-1919.
14.
Qanddoumi I, Orisme W, Wen J, Santiago T, Gupta K, Dalton JD, Tang B, Haupfear K, Punchihewa C, Easton J, Mulder H, Boggs K, Shao Y, Rusch M, Becksfort J, Gupta P, Wang S, Lee RP, Brat D, Collins VP, Dahiya S, George D, Konomos W, Kurian KM, McFadden K, Serafini LN, Nickols H, Perry A, Shurtleff S, Gajjar A, Boop FA, Klimo Jr PD, Mardis ER, Wilson RK, Baker SJ, Zhang J, Wu G, Downing JR, Tatevossian RG, Ellison DW. Genetic alterations in uncommon low grade neuroepithelial tumours: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology. Acta Neuropathol 2016; 131: 833-845.
15.
Schurr J, Coras R, Rossler K, Pieper T, Kudernatsch M, Holthausen H, Winkler P, Woermann F, Bien CG, Polster T, Schulz R, Kalbhenn T, Urbach H, Becker A, Grunwald T, Huppertz HJ, Gil-Nagel A, Toledano R, Feucht M, Mühlebner A, Czech T, Blümcke I. Mild malformation of cortical development with oligodendroglial hyperplasia in frontal lobe epilepsy: a new clinic-pathological entity. Brain Pathol 2017; 27: 26-35.
16.
Seetharam R, Nooraine J, Mhatre R, Ramachandran J, Iyer RB, Mahadevan A. Mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE): a widespread disease with an apparently focal epilepsy. Epileptic Disord 2021; 23: 407-411.
17.
Thom M, Liu J, Bongaarts A, Reinten RJ, Paradiso B, Jäger HR, Reeves C, Somani A, An S, Marsdon D, McEvoy A, Miserocchi A, Thorne L, Newman F, Bucur S, Honavar M, Jacques T, Aronica E. Multinodular and vacuolating neuronal tumours in epilepsy: dysplasia or neoplasia? Brain Pathol 2018; 28: 155-171.
18.
Thom M, Sisodiya S, Harkness W, Scaravilli F. Microdysgenesis in temporal lobe epilepsy. A quantitative and immunohistochemical study of white matter neurones. Brain 2001; 124: 2299-2309.
19.
Verentzioti A, Blumcke I, Alexoudi A, Patrikelis P, Siatouni A, Korfias S, Sakas D, Gatzonis S. Epileptic patient with mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE): A case report and review of the literature. Case Rep Neurol Med 2019; 2019: 9130780.
