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Suman Jayadev

Showing results (61-70 of 112) with videos related to

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Journal of Huntington'S Disease|April 13, 2025
Asymmetric brain atrophy in Huntington's disease: A postmortem MRI studyEardi Lila, David Hunt, Daniel D Child, et al.
Acta Neuropathologica|September 4, 2025
Down syndrome and a presenilin 2 variant: dual genetic risk of Alzheimer's diseaseJordan Ogg, Nadia Postupna, Laura E Gibbons, et al.
JAMA Ophthalmology|June 11, 2026
Quantitative Swept-Source Optical Coherence Tomography Angiography Indicators of Neurovascular Dysfunction in Alzheimer DiseaseYi Zhang, Yu Jiang, Kiumars Edalati, et al.
Annals of Neurology|March 19, 2011
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotypeSuman Jayadev, David Nochlin, Parvoneh Poorkaj, et al.
Parkinsonism & Related Disorders|October 1, 2020
Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's diseaseOswaldo Lorenzo-Betancor, Yi-Han Lin, Ali Samii, et al.
Journal of Alzheimer'S Disease : JAD|April 23, 2025
Plasma TAR DNA-binding protein 43 (TDP-43) levels in a population-based cohort of older adults: The cardiovascular health studyAlison E Fohner, Colleen M Sitlani, Suman Jayadev, et al.
Acta Neuropathologica|July 3, 2026
Mutation-specific neuropathologic signatures in MAPT-associated frontotemporal lobar degenerationMarika Bogdani, Vaishnavi S Jadhav, Brian C Kraemer, et al.
Journal of Alzheimer'S Disease : JAD|August 4, 2020
Early-Onset Familial Alzheimer Disease Variant PSEN2 N141I Heterozygosity is Associated with Altered Microglia PhenotypeSusan Fung, Carole L Smith, Katherine E Prater, et al.
Journal of Huntington'S Disease|October 3, 2017
Enhanced retinal responses in Huntington's disease patientsJocelynn R Pearl, Laura M Heath, Dani E Bergey, et al.
Glia|May 21, 2011
Transcription factor p53 influences microglial activation phenotypeSuman Jayadev, Nicole K Nesser, Stephanie Hopkins, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Journal of Huntington'S Disease|April 13, 2025
Asymmetric brain atrophy in Huntington's disease: A postmortem MRI studyEardi Lila, David Hunt, Daniel D Child, et al.
Acta Neuropathologica|September 4, 2025
Down syndrome and a presenilin 2 variant: dual genetic risk of Alzheimer's diseaseJordan Ogg, Nadia Postupna, Laura E Gibbons, et al.
JAMA Ophthalmology|June 11, 2026
Quantitative Swept-Source Optical Coherence Tomography Angiography Indicators of Neurovascular Dysfunction in Alzheimer DiseaseYi Zhang, Yu Jiang, Kiumars Edalati, et al.
Annals of Neurology|March 19, 2011
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotypeSuman Jayadev, David Nochlin, Parvoneh Poorkaj, et al.
Parkinsonism & Related Disorders|October 1, 2020
Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's diseaseOswaldo Lorenzo-Betancor, Yi-Han Lin, Ali Samii, et al.
Journal of Alzheimer'S Disease : JAD|April 23, 2025
Plasma TAR DNA-binding protein 43 (TDP-43) levels in a population-based cohort of older adults: The cardiovascular health studyAlison E Fohner, Colleen M Sitlani, Suman Jayadev, et al.
Acta Neuropathologica|July 3, 2026
Mutation-specific neuropathologic signatures in MAPT-associated frontotemporal lobar degenerationMarika Bogdani, Vaishnavi S Jadhav, Brian C Kraemer, et al.
Journal of Alzheimer'S Disease : JAD|August 4, 2020
Early-Onset Familial Alzheimer Disease Variant PSEN2 N141I Heterozygosity is Associated with Altered Microglia PhenotypeSusan Fung, Carole L Smith, Katherine E Prater, et al.
Journal of Huntington'S Disease|October 3, 2017
Enhanced retinal responses in Huntington's disease patientsJocelynn R Pearl, Laura M Heath, Dani E Bergey, et al.
Glia|May 21, 2011
Transcription factor p53 influences microglial activation phenotypeSuman Jayadev, Nicole K Nesser, Stephanie Hopkins, et al.
Pageof 12