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Allele-specific RNAi Targeting of a PRNP Genetic Variant that Causes Gerstmann–Sträussler–Scheinker Disease

Author:LoPresti, Patrizia   Qin, Kefeng   Mastrianni, James   

Session Name:P5: Aging, Dementia, and Behavioral Neurology: Genetics  

Topic:Headache  

Program Number:P5.006  

Author Institution:

Association of EPG5 Variants with Neurodegenerative Diseases in the All of Us Research Program

Author:Shin, SungJin   Bean, Elizabeth   Grlickova-Duzevik, Eliza   Cao, Ling   

Session Name:P5: Aging, Dementia, and Behavioral Neurology: Genetics  

Topic:Movement Disorders  

Program Number:P5.007  

Author Institution:

Biological Sex Influences the Clinical Phenotype of AD and FTD Spectrum Disorders

Author:Jang, Kaitlyn   Berendzen, Kristen   Allen, Isabel   Fischer, Luke   Mauer, Ezra   Chapleau, Marianne   Montembeault, Maxime   Casaletto, Kaitlin   Sturm, Virginia   Seeley, William   LaJoie, Renaud   Rabinovici, Gil   Miller, Bruce   Gorno Tempini, Maria Luisa   Miller, Zachary   

Session Name:P5: Aging, Dementia, and Behavioral Neurology: Genetics  

Topic:Infectious Disease  

Program Number:P5.008  

Author Institution:

Pure Word Deafness in Epileptic Encephalopathy Associated with a SCAF4 Variant: A Case Report

Author:Zarate, Carlos   Garcia Velazquez, Sandra   Parker, Alicia   

Session Name:P5: Aging, Dementia, and Behavioral Neurology: Genetics  

Topic:Multiple Sclerosis  

Program Number:P5.009  

Author Institution:

Investigating the Role of S100A1 Depletion in a Mouse Model of Vascular Dementia

Author:Nisar, Sana   Nisar, Mohammad   Murudkar, Tej   

Session Name:P5: Aging, Dementia, and Behavioral Neurology: Genetics  

Topic:Movement Disorders  

Program Number:P5.010  

Author Institution: