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Manuela Neumann

Showing results (161-170 of 175) with videos related to

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Neuro-Oncology Advances|March 14, 2023
Clinical outcome of biomarker-guided therapies in adult patients with tumors of the nervous systemMirjam Renovanz, Sylvia C Kurz, Johannes Rieger, et al.
Acta Neuropathologica|August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-USara Alidadiani, Júlia Faura, Sarah Wynants, et al.
Acta Neuropathologica|December 13, 2022
LATE-NC staging in routine neuropathologic diagnosis: an updatePeter T Nelson, Edward B Lee, Matthew D Cykowski, et al.
Acta Neuropathologica|May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationHazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Nature Medicine|June 18, 2024
Plasma extracellular vesicle tau and TDP-43 as diagnostic biomarkers in FTD and ALSMadhurima Chatterjee, Selcuk Özdemir, Christian Fritz, et al.
Acta Neuropathologica|February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLDCyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Pageof 18

Showing results (161-170 of 175) with videos related to

Sort By:
Pageof 18
Neuro-Oncology Advances|March 14, 2023
Clinical outcome of biomarker-guided therapies in adult patients with tumors of the nervous systemMirjam Renovanz, Sylvia C Kurz, Johannes Rieger, et al.
Acta Neuropathologica|August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-USara Alidadiani, Júlia Faura, Sarah Wynants, et al.
Acta Neuropathologica|December 13, 2022
LATE-NC staging in routine neuropathologic diagnosis: an updatePeter T Nelson, Edward B Lee, Matthew D Cykowski, et al.
Acta Neuropathologica|May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationHazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Nature Medicine|June 18, 2024
Plasma extracellular vesicle tau and TDP-43 as diagnostic biomarkers in FTD and ALSMadhurima Chatterjee, Selcuk Özdemir, Christian Fritz, et al.
Acta Neuropathologica|February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLDCyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Pageof 18