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Sigrun Roeber

Showing results (21-30 of 80) with videos related to

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Journal of Proteome Research|February 25, 2012
Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degenerationDaniel Martins-de-Souza, Paul C Guest, David M Mann, et al.
Journal of Neuropathology and Experimental Neurology|October 18, 2011
α-Internexin in the diagnosis of oligodendroglial tumors and association with 1p/19q statusSabina Eigenbrod, Sigrun Roeber, Niklas Thon, et al.
Neurobiology of Aging|June 28, 2020
Somatosensory area 3b is selectively unaffected in corticobasal syndrome: combining MRI and histologyLars Dinkelbach, Martin Südmeyer, Christian Johannes Hartmann, et al.
Frontiers in Neurology|June 2, 2017
Transient Vestibulopathy in Wallenberg's Syndrome: Pathologic AnalysisJorge C Kattah, Ali S Saber Tehrani, Sigrun Roeber, et al.
Acta Neuropathologica|August 17, 2022
Single-nucleus chromatin accessibility profiling highlights distinct astrocyte signatures in progressive supranuclear palsy and corticobasal degenerationNils Briel, Viktoria C Ruf, Katrin Pratsch, et al.
Brain : a Journal of Neurology|May 25, 2006
Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJDAnna Krasnianski, Walter J Schulz-Schaeffer, Kai Kallenberg, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 10, 2015
Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's diseaseSigrun Roeber, Felix Müller-Sarnowski, Julia Kress, et al.
Journal of the Neurological Sciences|November 5, 2011
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entityChristina Sundal, Jennifer Lash, Jan Aasly, et al.
Plos One|May 15, 2008
Evidence for a pathogenic role of different mutations at codon 188 of PRNPSigrun Roeber, Eva-Maria Grasbon-Frodl, Otto Windl, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2013
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and neuroprotection and natural history in Parkinson plus syndromes criteria for the diagnosis of progressive supranuclear palsyGesine Respondek, Sigrun Roeber, Hans Kretzschmar, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Journal of Proteome Research|February 25, 2012
Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degenerationDaniel Martins-de-Souza, Paul C Guest, David M Mann, et al.
Journal of Neuropathology and Experimental Neurology|October 18, 2011
α-Internexin in the diagnosis of oligodendroglial tumors and association with 1p/19q statusSabina Eigenbrod, Sigrun Roeber, Niklas Thon, et al.
Neurobiology of Aging|June 28, 2020
Somatosensory area 3b is selectively unaffected in corticobasal syndrome: combining MRI and histologyLars Dinkelbach, Martin Südmeyer, Christian Johannes Hartmann, et al.
Frontiers in Neurology|June 2, 2017
Transient Vestibulopathy in Wallenberg's Syndrome: Pathologic AnalysisJorge C Kattah, Ali S Saber Tehrani, Sigrun Roeber, et al.
Acta Neuropathologica|August 17, 2022
Single-nucleus chromatin accessibility profiling highlights distinct astrocyte signatures in progressive supranuclear palsy and corticobasal degenerationNils Briel, Viktoria C Ruf, Katrin Pratsch, et al.
Brain : a Journal of Neurology|May 25, 2006
Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJDAnna Krasnianski, Walter J Schulz-Schaeffer, Kai Kallenberg, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 10, 2015
Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's diseaseSigrun Roeber, Felix Müller-Sarnowski, Julia Kress, et al.
Journal of the Neurological Sciences|November 5, 2011
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entityChristina Sundal, Jennifer Lash, Jan Aasly, et al.
Plos One|May 15, 2008
Evidence for a pathogenic role of different mutations at codon 188 of PRNPSigrun Roeber, Eva-Maria Grasbon-Frodl, Otto Windl, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2013
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and neuroprotection and natural history in Parkinson plus syndromes criteria for the diagnosis of progressive supranuclear palsyGesine Respondek, Sigrun Roeber, Hans Kretzschmar, et al.
Pageof 8