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Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay.
Kobow K, Jabari S, Pieper T, Kudernatsch M, Polster T, Woermann FG, Kalbhenn T, Hamer H, Rössler K, Mühlebner A, Spliet WGM, Feucht M, Hou Y, Stichel D, Korshunov A, Sahm F, Coras R, Blümcke I, von Deimling A. Kobow K, et al. Among authors: feucht m. Acta Neuropathol. 2020 Dec;140(6):881-891. doi: 10.1007/s00401-020-02228-5. Epub 2020 Sep 26. Acta Neuropathol. 2020. PMID: 32979071 Free PMC article.
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. Schurr J, et al. Among authors: feucht m. Brain Pathol. 2017 Jan;27(1):26-35. doi: 10.1111/bpa.12347. Epub 2016 Feb 22. Brain Pathol. 2017. PMID: 26748554 Free PMC article.
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; EEBB Consortium. Blumcke I, et al. Among authors: feucht m. N Engl J Med. 2017 Oct 26;377(17):1648-1656. doi: 10.1056/NEJMoa1703784. N Engl J Med. 2017. PMID: 29069555 Free article.
DNA methylation-based classification of malformations of cortical development in the human brain.
Jabari S, Kobow K, Pieper T, Hartlieb T, Kudernatsch M, Polster T, Bien CG, Kalbhenn T, Simon M, Hamer H, Rössler K, Feucht M, Mühlebner A, Najm I, Peixoto-Santos JE, Gil-Nagel A, Delgado RT, Aledo-Serrano A, Hou Y, Coras R, von Deimling A, Blümcke I. Jabari S, et al. Among authors: feucht m. Acta Neuropathol. 2022 Jan;143(1):93-104. doi: 10.1007/s00401-021-02386-0. Epub 2021 Nov 19. Acta Neuropathol. 2022. PMID: 34797422 Free PMC article.
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. Mühlebner A, et al. Among authors: feucht m. Acta Neuropathol. 2012 Feb;123(2):259-72. doi: 10.1007/s00401-011-0920-1. Epub 2011 Nov 27. Acta Neuropathol. 2012. PMID: 22120580
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. Kobow K, et al. Among authors: feucht m. Epilepsia. 2019 Jun;60(6):1091-1103. doi: 10.1111/epi.14934. Epub 2019 May 10. Epilepsia. 2019. PMID: 31074842 Free PMC article.
Epilepsy surgery in children and adolescents with malformations of cortical development--outcome and impact of the new ILAE classification on focal cortical dysplasia.
Mühlebner A, Gröppel G, Dressler A, Reiter-Fink E, Kasprian G, Prayer D, Dorfer C, Czech T, Hainfellner JA, Coras R, Blümcke I, Feucht M. Mühlebner A, et al. Among authors: feucht m. Epilepsy Res. 2014 Nov;108(9):1652-61. doi: 10.1016/j.eplepsyres.2014.08.012. Epub 2014 Aug 30. Epilepsy Res. 2014. PMID: 25219355
Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis omplex (TSC): evidence from layer-specific marker expression.
Mühlebner A, Iyer AM, van Scheppingen J, Anink JJ, Jansen FE, Veersema TJ, Braun KP, Spliet WG, van Hecke W, Söylemezoğlu F, Feucht M, Krsek P, Zamecnik J, Bien CG, Polster T, Coras R, Blümcke I, Aronica E. Mühlebner A, et al. Among authors: feucht m. J Neurodev Disord. 2016 Apr 1;8:9. doi: 10.1186/s11689-016-9142-0. eCollection 2016. J Neurodev Disord. 2016. PMID: 27042238 Free PMC article.
Impaired myelin production due to an intrinsic failure of oligodendrocytes in mTORpathies.
Gruber VE, Lang J, Endmayr V, Diehm R, Pimpel B, Glatter S, Anink JJ, Bongaarts A, Luinenburg MJ, Reinten RJ, van der Wel N, Larsen P, Hainfellner JA, Rössler K, Aronica E, Scholl T, Mühlebner A, Feucht M. Gruber VE, et al. Among authors: feucht m. Neuropathol Appl Neurobiol. 2021 Oct;47(6):812-825. doi: 10.1111/nan.12744. Epub 2021 Jul 26. Neuropathol Appl Neurobiol. 2021. PMID: 34173252 Free PMC article.
342 results