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Suman Jayadev

Showing results (31-40 of 112) with videos related to

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Cerebellum (London, England)|September 10, 2017
Psychosis in Spinocerebellar Ataxias: a Case Series and Study of Tyrosine Hydroxylase in Substantia NigraKatherine W Turk, Margaret E Flanagan, Samuel Josephson, et al.
Brain : a Journal of Neurology|August 11, 2022
Aberrant splicing of PSEN2, but not PSEN1, in individuals with sporadic Alzheimer's diseaseMeredith M Course, Kathryn Gudsnuk, C Dirk Keene, et al.
Journal of Huntington'S Disease|August 9, 2021
Subdural Hematoma as a Serious Complication of Huntington's Disease: An Observational StudyMarie Davis, Vicki Wheelock, Lauren Talman, et al.
Neurology. Genetics|May 27, 2022
Progress in Amyotrophic Lateral Sclerosis Gene Discovery: Reflecting on Classic Approaches and Leveraging Emerging TechnologiesSamuel N Smukowski, Heather Maioli, Caitlin S Latimer, et al.
American Journal of Medical Genetics. Part A|November 2, 2017
Novel pregnancy-triggered episodes of CAPOS syndromeIrene J Chang, Margaret P Adam, Suman Jayadev, et al.
Glia|April 4, 2025
The Alzheimer's Disease Gene SORL1 Regulates Lysosome Function in Human MicrogliaSwati Mishra, Nader Morshed, Sonia Beant Sidhu, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Chronic evoked seizures in young pre-symptomatic APP/PS1 mice induce serotonin changes and accelerate onset on Alzheimer's disease-related neurpathologyAaron Del Pozo, Kevin M Knox, Leanne Lehmann, et al.
Journal of Alzheimer'S Disease : JAD|June 3, 2025
Alzheimer's disease-associated genotypes differentially influence chronic evoked seizure outcomes and antiseizure medicine efficacy in aged miceKevin M Knox, Stephanie Davidson, Leanne M Lehmann, et al.
Archives of Neurology|March 12, 2008
Conjugal Alzheimer disease: risk in children when both parents have Alzheimer diseaseSuman Jayadev, Ellen J Steinbart, Yueh-Yun Chi, et al.
Brain : a Journal of Neurology|April 9, 2010
Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2Suman Jayadev, James B Leverenz, Ellen Steinbart, et al.
Pageof 12

Showing results (31-40 of 112) with videos related to

Sort By:
Pageof 12
Cerebellum (London, England)|September 10, 2017
Psychosis in Spinocerebellar Ataxias: a Case Series and Study of Tyrosine Hydroxylase in Substantia NigraKatherine W Turk, Margaret E Flanagan, Samuel Josephson, et al.
Brain : a Journal of Neurology|August 11, 2022
Aberrant splicing of PSEN2, but not PSEN1, in individuals with sporadic Alzheimer's diseaseMeredith M Course, Kathryn Gudsnuk, C Dirk Keene, et al.
Journal of Huntington'S Disease|August 9, 2021
Subdural Hematoma as a Serious Complication of Huntington's Disease: An Observational StudyMarie Davis, Vicki Wheelock, Lauren Talman, et al.
Neurology. Genetics|May 27, 2022
Progress in Amyotrophic Lateral Sclerosis Gene Discovery: Reflecting on Classic Approaches and Leveraging Emerging TechnologiesSamuel N Smukowski, Heather Maioli, Caitlin S Latimer, et al.
American Journal of Medical Genetics. Part A|November 2, 2017
Novel pregnancy-triggered episodes of CAPOS syndromeIrene J Chang, Margaret P Adam, Suman Jayadev, et al.
Glia|April 4, 2025
The Alzheimer's Disease Gene SORL1 Regulates Lysosome Function in Human MicrogliaSwati Mishra, Nader Morshed, Sonia Beant Sidhu, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Chronic evoked seizures in young pre-symptomatic APP/PS1 mice induce serotonin changes and accelerate onset on Alzheimer's disease-related neurpathologyAaron Del Pozo, Kevin M Knox, Leanne Lehmann, et al.
Journal of Alzheimer'S Disease : JAD|June 3, 2025
Alzheimer's disease-associated genotypes differentially influence chronic evoked seizure outcomes and antiseizure medicine efficacy in aged miceKevin M Knox, Stephanie Davidson, Leanne M Lehmann, et al.
Archives of Neurology|March 12, 2008
Conjugal Alzheimer disease: risk in children when both parents have Alzheimer diseaseSuman Jayadev, Ellen J Steinbart, Yueh-Yun Chi, et al.
Brain : a Journal of Neurology|April 9, 2010
Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2Suman Jayadev, James B Leverenz, Ellen Steinbart, et al.
Pageof 12