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Roland Coras

Showing results (121-130 of 163) with videos related to

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Journal of Neurodevelopmental Disorders|April 5, 2016
Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis omplex (TSC): evidence from layer-specific marker expressionAngelika Mühlebner, Anand M Iyer, Jackelien van Scheppingen, 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.
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.
Brain : a Journal of Neurology|September 14, 2010
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseasesChristoph S Clemen, Karthikeyan Tangavelou, Karl-Heinz Strucksberg, et al.
Acta Neuropathologica|March 27, 2023
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.
Acta Neuropathologica|February 2, 2024
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patientsLaura Krumm, Tatyana Pozner, Naime Zagha, et al.
Acta Neuropathologica Communications|November 10, 2023
Deep histopathology genotype-phenotype analysis of focal cortical dysplasia type II differentiates between the GATOR1-altered autophagocytic subtype IIa and MTOR-altered migration deficient subtype IIbJonas Honke, Lucas Hoffmann, Roland Coras, et al.
Cell|September 4, 2018
Neurons under T Cell Attack Coordinate Phagocyte-Mediated Synaptic StrippingGiovanni Di Liberto, Stanislav Pantelyushin, Mario Kreutzfeldt, et al.
Translational Neuroscience|January 29, 2024
Brain expression profiles of two <i>SCN1A</i> antisense RNAs in children and adolescents with epilepsyMarius Frederik Schneider, Miriam Vogt, Johanna Scheuermann, et al.
Nature Communications|November 30, 2024
Analysis of 1386 epileptogenic brain lesions reveals association with DYRK1A and EGFRChristian M Boßelmann, Costin Leu, Tobias Brünger, et al.
Pageof 17

Showing results (121-130 of 163) with videos related to

Sort By:
Pageof 17
Journal of Neurodevelopmental Disorders|April 5, 2016
Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis omplex (TSC): evidence from layer-specific marker expressionAngelika Mühlebner, Anand M Iyer, Jackelien van Scheppingen, 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.
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.
Brain : a Journal of Neurology|September 14, 2010
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseasesChristoph S Clemen, Karthikeyan Tangavelou, Karl-Heinz Strucksberg, et al.
Acta Neuropathologica|March 27, 2023
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.
Acta Neuropathologica|February 2, 2024
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patientsLaura Krumm, Tatyana Pozner, Naime Zagha, et al.
Acta Neuropathologica Communications|November 10, 2023
Deep histopathology genotype-phenotype analysis of focal cortical dysplasia type II differentiates between the GATOR1-altered autophagocytic subtype IIa and MTOR-altered migration deficient subtype IIbJonas Honke, Lucas Hoffmann, Roland Coras, et al.
Cell|September 4, 2018
Neurons under T Cell Attack Coordinate Phagocyte-Mediated Synaptic StrippingGiovanni Di Liberto, Stanislav Pantelyushin, Mario Kreutzfeldt, et al.
Translational Neuroscience|January 29, 2024
Brain expression profiles of two <i>SCN1A</i> antisense RNAs in children and adolescents with epilepsyMarius Frederik Schneider, Miriam Vogt, Johanna Scheuermann, et al.
Nature Communications|November 30, 2024
Analysis of 1386 epileptogenic brain lesions reveals association with DYRK1A and EGFRChristian M Boßelmann, Costin Leu, Tobias Brünger, et al.
Pageof 17