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Showing results (371-380 of 448) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
FTLD targets brain regions expressing recently evolved genesLorenzo Pasquini, Felipe L Pereira, Sahba Seddighi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 2, 2013
TDP-43 frontotemporal lobar degeneration and autoimmune diseaseZachary A Miller, Katherine P Rankin, Neill R Graff-Radford, et al.
Yonsei Medical Journal|November 20, 2018
The Brain Donation Program in South KoreaYeshin Kim, Yeon Lim Suh, Seung Joo Kim, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Transplantation of Human IPSC-derived Microglia Ameliorates Neuropathology and Circuit Dysfunction in Progranulin-Deficient MiceHayk Davtyan, Sarah Naguib, Yuliya Voskobiynyk, et al.
Research Square|February 13, 2026
Transplantation of Human IPSC-derived Microglia Ameliorates Neuropathology and Circuit Dysfunction in Progranulin-Deficient MiceHayk Davtyan, Sarah Naguib, Yuliya Voskobiynyk, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Alterations in Lysosomal, Glial and Neurodegenerative Biomarkers in Patients with Sporadic and Genetic Forms of Frontotemporal DementiaJennifer Hsiao-Nakamoto, Chi-Lu Chiu, Lawren VandeVrede, et al.
JAMA Network Open|April 29, 2022
Diagnostic Accuracy of Magnetic Resonance Imaging Measures of Brain Atrophy Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal DegenerationIgnacio Illán-Gala, Salvatore Nigro, Lawren VandeVrede, et al.
Acta Neuropathologica|November 2, 2018
Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementiaEthan G Geier, Mathieu Bourdenx, Nadia J Storm, et al.
Brain : a Journal of Neurology|July 5, 2015
The behavioural/dysexecutive variant of Alzheimer's disease: clinical, neuroimaging and pathological featuresRik Ossenkoppele, Yolande A L Pijnenburg, David C Perry, et al.
Brain : a Journal of Neurology|February 14, 2015
Defects of mutant DNMT1 are linked to a spectrum of neurological disordersJonathan Baets, Xiaohui Duan, Yanhong Wu, et al.
Pageof 45

Showing results (371-380 of 448) with videos related to

Sort By:
Pageof 45
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
FTLD targets brain regions expressing recently evolved genesLorenzo Pasquini, Felipe L Pereira, Sahba Seddighi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 2, 2013
TDP-43 frontotemporal lobar degeneration and autoimmune diseaseZachary A Miller, Katherine P Rankin, Neill R Graff-Radford, et al.
Yonsei Medical Journal|November 20, 2018
The Brain Donation Program in South KoreaYeshin Kim, Yeon Lim Suh, Seung Joo Kim, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Transplantation of Human IPSC-derived Microglia Ameliorates Neuropathology and Circuit Dysfunction in Progranulin-Deficient MiceHayk Davtyan, Sarah Naguib, Yuliya Voskobiynyk, et al.
Research Square|February 13, 2026
Transplantation of Human IPSC-derived Microglia Ameliorates Neuropathology and Circuit Dysfunction in Progranulin-Deficient MiceHayk Davtyan, Sarah Naguib, Yuliya Voskobiynyk, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Alterations in Lysosomal, Glial and Neurodegenerative Biomarkers in Patients with Sporadic and Genetic Forms of Frontotemporal DementiaJennifer Hsiao-Nakamoto, Chi-Lu Chiu, Lawren VandeVrede, et al.
JAMA Network Open|April 29, 2022
Diagnostic Accuracy of Magnetic Resonance Imaging Measures of Brain Atrophy Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal DegenerationIgnacio Illán-Gala, Salvatore Nigro, Lawren VandeVrede, et al.
Acta Neuropathologica|November 2, 2018
Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementiaEthan G Geier, Mathieu Bourdenx, Nadia J Storm, et al.
Brain : a Journal of Neurology|July 5, 2015
The behavioural/dysexecutive variant of Alzheimer's disease: clinical, neuroimaging and pathological featuresRik Ossenkoppele, Yolande A L Pijnenburg, David C Perry, et al.
Brain : a Journal of Neurology|February 14, 2015
Defects of mutant DNMT1 are linked to a spectrum of neurological disordersJonathan Baets, Xiaohui Duan, Yanhong Wu, et al.
Pageof 45