The genomic landscape across 474 surgically accessible epileptogenic human brain lesions.
López-Rivera, JA; Leu, C; Macnee, M; Khoury, J; Hoffmann, L; Coras, R; Kobow, K; Bhattarai, N; Pérez-Palma, E; Hamer, H; Brandner, S; Rössler, K; Bien, CG; Kalbhenn, T; Pieper, T; Hartlieb, T; Butler, E; Genovese, G; Becker, K; Altmüller, J; Niestroj, LM; Ferguson, L; Busch, RM; Nürnberg, P; Najm, I; Blümcke, I; Lal, D;
Brain. 2022;
Originalarbeiten (Zeitschrift)

Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
Bonduelle, T; Hartlieb, T; Baldassari, S; Sim, NS; Kim, SH; Kang, HC; Kobow, K; Coras, R; Chipaux, M; Dorfmuller, G; Adle-Biassette, H; Aronica, E; Lee, JH; Blumcke, I; Baulac, S
ACTA NEUROPATHOL COM. 2021; 9(1): 3
Originalarbeiten (Zeitschrift)

Dysmorphic neurons as cellular source for phase-amplitude coupling in Focal Cortical Dysplasia Type II.
Rampp, S; Rössler, K; Hamer, H; Illek, M; Buchfelder, M; Doerfler, A; Pieper, T; Hartlieb, T; Kudernatsch, M; Koelble, K; Peixoto-Santos, JE; Blümcke, I; Coras, R;
Clin Neurophysiol. 2021; 132(3): 782-792.
Originalarbeiten (Zeitschrift)

Repetitive miniature spikes - An underreported EEG pattern
Unterberger, I; Kaplan, PW; Luef, G; Trinka, E; Walser, G; Bauer, G
CLIN NEUROPHYSIOL. 2020; 131(1): 40-45.
Originalarbeiten (Zeitschrift)

Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasia.
Kobow, K; Ziemann, M; Kaipananickal, H; Khurana, I; Mühlebner, A; Feucht, M; Hainfellner, JA; Czech, T; Aronica, E; Pieper, T; Holthausen, H; Kudernatsch, M; Hamer, H; Kasper, BS; Rössler, K; Conti, V; Guerrini, R; Coras, R; Blümcke, I; El-Osta, A; Kaspi, A;
Epilepsia. 2019; 60(6):109-1103
Originalarbeiten (Zeitschrift)

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery.
Blumcke, I; Spreafico, R; Haaker, G; Coras, R; Kobow, K; Bien, CG; Pfäfflin, M; Elger, C; Widman, G; Schramm, J; Becker, A; Braun, KP; Leijten, F; Baayen, JC; Aronica, E; Chassoux, F; Hamer, H; Stefan, H; Rössler, K; Thom, M; Walker, MC; Sisodiya, SM; Duncan, JS; McEvoy, AW; Pieper, T; Holthausen, H; Kudernatsch, M; Meencke, HJ; Kahane, P; Schulze-Bonhage, A; Zentner, J; Heiland, DH; Urbach, H; Steinhoff, BJ; Bast, T; Tassi, L; Lo Russo, G; Özkara, C; Oz, B; Krsek, P; Vogelgesang, S; Runge, U; Lerche, H; Weber, Y; Honavar, M; Pimentel, J; Arzimanoglou, A; Ulate-Campos, A; Noachtar, S; Hartl, E; Schijns, O; Guerrini, R; Barba, C; Jacques, TS; Cross, JH; Feucht, M; Mühlebner, A; Grunwald, T; Trinka, E; Winkler, PA; Gil-Nagel, A; Toledano Delgado, R; Mayer, T; Lutz, M; Zountsas, B; Garganis, K; Rosenow, F; Hermsen, A; von Oertzen, TJ; Diepgen, TL; Avanzini, G;
N Engl J Med. 2017; 377(17):1648-1656
Originalarbeiten (Zeitschrift)

Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological Entity.
Schurr, J; Coras, R; Rössler, 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;
Brain Pathol. 2017; 27(1):26-35
Originalarbeiten (Zeitschrift)

Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.
Nicita, F; Garone, G; Spalice, A; Savasta, S; Striano, P; Pantaleoni, C; Spartà, MV; Kluger, G; Capovilla, G; Pruna, D; Freri, E; D"Arrigo, S; Verrotti, A;
Am J Med Genet A. 2016; 170(1):148-155
Originalarbeiten (Zeitschrift)

Calcium-binding proteins in focal cortical dysplasia.
Kuchukhidze, G; Wieselthaler-Holzl, A; Drexel, M; Unterberger, I; Luef, G; Ortler, M; Becker, AJ; Trinka, E; Sperk, G
Epilepsia. 2015; 56(8):1207-1216
Originalarbeiten (Zeitschrift)

Co-occurring malformations of cortical development and SCN1A gene mutations.
Barba, C; Parrini, E; Coras, R; Galuppi, A; Craiu, D; Kluger, G; Parmeggiani, A; Pieper, T; Schmitt-Mechelke, T; Striano, P; Giordano, F; Blumcke, I; Guerrini, R;
Epilepsia. 2014; 55(7): 1009-1019.
Originalarbeiten (Zeitschrift)

Electro-clinical-pathological correlations in focal cortical dysplasia (FCD) at young ages.
Holthausen, H; Pieper, T; Winkler, P; Bluemcke, I; Kudernatsch, M;
Childs Nerv Syst. 2014; 30(12):2015-2026
Übersichtsarbeiten

Towards early diagnosis and treatment to save children from catastrophic epilepsy -- focus on epilepsy surgery.
Holthausen, H; Pieper, T; Kudernatsch, M;
Brain Dev. 2013; 35(8):730-741
Übersichtsarbeiten

Neuropathologic measurements in focal cortical dysplasias: validation of the ILAE 2011 classification system and diagnostic implications for MRI.
Mühlebner, A; Coras, R; Kobow, K; Feucht, M; Czech, T; Stefan, H; Weigel, D; Buchfelder, M; Holthausen, H; Pieper, T; Kudernatsch, M; Blümcke, I;
Acta Neuropathol. 2012; 123(2):259-272
Originalarbeiten (Zeitschrift)

A distinct variant of focal cortical dysplasia type I characterised by magnetic resonance imaging and neuropathological examination in children with severe epilepsies.
Blümcke, I; Pieper, T; Pauli, E; Hildebrandt, M; Kudernatsch, M; Winkler, P; Karlmeier, A; Holthausen, H;
Epileptic Disord. 2010; 12(3):172-180
Originalarbeiten (Zeitschrift)

Hippocampal abnormalities in malformations of cortical development: MRI study.
Kuchukhidze, G; Koppelstaetter, F; Unterberger, I; Dobesberger, J; Walser, G; Zamarian, L; Haberlandt, E; Maier, H; Ortler, M; Gotwald, T; Gelpi, E; Czech, T; Feucht, M; Bauer, G; Delazer, M; Felber, S; Trinka, E;
Neurology. 2010; 74(20): 1575-1582.
Originalarbeiten (Zeitschrift)

Reduction of benzodiazepine receptor binding is related to the seizure onset zone in extratemporal focal cortical dysplasia.
Arnold, S; Berthele, A; Drzezga, A; Tölle, TR; Weis, S; Werhahn, KJ; Henkel, A; Yousry, TA; Winkler, PA; Bartenstein, P; Noachtar, S;
Epilepsia. 2000; 41(7): 818-824.
Originalarbeiten (Zeitschrift)