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Brain somatic variants in human focal epilepsy
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(6)
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Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) (2021)
Bonduelle T, Hartlieb T, Baldassari S, Sim NS, Kim SH, Kang HC, Kobow K, et al.
Journal article
Molecular diagnostics in drug-resistant focal epilepsy define new disease entities. (2021)
Kobow K, Baulac S, von Deimling A, Lee JH
Journal article
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay (2020)
Kobow K, Jabari S, Pieper T, Kudernatsch M, Polster T, Woermann FG, Kalbhenn T, et al.
Journal article
A comprehensive clinico-pathological and genetic evaluation of bottom-of-sulcus focal cortical dysplasia in patients with difficult-to-localize focal epilepsy (2019)
Ying Z, Wang I, Blümcke I, Bulacio J, Alexopoulos A, Jehi L, Bingaman W, et al.
Journal article
Assessment of genetic variant burden in epilepsy-associated brain lesions (2019)
Niestroj LM, May P, Artomov M, Kobow K, Coras R, Pérez-Palma E, Altmüller J, et al.
Journal article
DISCOVERY AND PATHOGENICITY ASSESSMENT OF NEUROPATHOLOGY-ASSOCIATED GENE VARIANTS (2017)
Neupert LM, May P, Kobow K, Nothnagel M, Nuernberg P, Freiman T, Harter P, et al.
Conference contribution