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Tom Pieper

Showing results (31-40 of 49) with videos related to

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Epilepsia|June 7, 2014
Co-occurring malformations of cortical development and SCN1A gene mutationsCarmen Barba, Elena Parrini, Roland Coras, et al.
Cells|June 10, 2023
Generation of Chimeric Antigen Receptors against Tetraspanin 7Tom Pieper, Kristian Daniel Ralph Roth, Viktor Glaser, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 11, 2021
Dysmorphic neurons as cellular source for phase-amplitude coupling in Focal Cortical Dysplasia Type IIStefan Rampp, Karl Rössler, Hajo Hamer, et al.
Epilepsia|November 6, 2021
Multilobar unilateral hypoplasia with emphasis on the posterior quadrant and severe epilepsy in children with FCD ILAE Type 1AHans Holthausen, Roland Coras, Yingying Tang, et al.
Epilepsia Open|June 7, 2024
Age-dependent increase of perineuronal nets in the human hippocampus and precocious aging in epilepsyAnnika Lehner, Lucas Hoffmann, Stefan Rampp, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 3, 2005
A semiological classification of status epilepticusSabine Rona, Felix Rosenow, Stephan Arnold, et al.
Acta Neuropathologica|September 26, 2020
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delayKatja Kobow, Samir Jabari, Tom Pieper, et al.
Epilepsia|May 11, 2019
Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasiaKatja Kobow, Mark Ziemann, Harikrishnan Kaipananickal, et al.
Brain Pathology (Zurich, Switzerland)|January 11, 2016
Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological EntityJohannes Schurr, Roland Coras, Karl Rössler, et al.
Acta Neuropathologica|April 28, 2023
Correction to: Ganglioglioma with adverse clinical outcome and atypical histopathological features were defined by alterations in PTPN11/KRAS/NF1 and other RAS-/MAP-Kinase pathway genesLucas Hoffmann, Roland Coras, Katja Kobow, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Epilepsia|June 7, 2014
Co-occurring malformations of cortical development and SCN1A gene mutationsCarmen Barba, Elena Parrini, Roland Coras, et al.
Cells|June 10, 2023
Generation of Chimeric Antigen Receptors against Tetraspanin 7Tom Pieper, Kristian Daniel Ralph Roth, Viktor Glaser, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 11, 2021
Dysmorphic neurons as cellular source for phase-amplitude coupling in Focal Cortical Dysplasia Type IIStefan Rampp, Karl Rössler, Hajo Hamer, et al.
Epilepsia|November 6, 2021
Multilobar unilateral hypoplasia with emphasis on the posterior quadrant and severe epilepsy in children with FCD ILAE Type 1AHans Holthausen, Roland Coras, Yingying Tang, et al.
Epilepsia Open|June 7, 2024
Age-dependent increase of perineuronal nets in the human hippocampus and precocious aging in epilepsyAnnika Lehner, Lucas Hoffmann, Stefan Rampp, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 3, 2005
A semiological classification of status epilepticusSabine Rona, Felix Rosenow, Stephan Arnold, et al.
Acta Neuropathologica|September 26, 2020
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delayKatja Kobow, Samir Jabari, Tom Pieper, et al.
Epilepsia|May 11, 2019
Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasiaKatja Kobow, Mark Ziemann, Harikrishnan Kaipananickal, et al.
Brain Pathology (Zurich, Switzerland)|January 11, 2016
Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological EntityJohannes Schurr, Roland Coras, Karl Rössler, et al.
Acta Neuropathologica|April 28, 2023
Correction to: Ganglioglioma with adverse clinical outcome and atypical histopathological features were defined by alterations in PTPN11/KRAS/NF1 and other RAS-/MAP-Kinase pathway genesLucas Hoffmann, Roland Coras, Katja Kobow, et al.
Pageof 5