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AFTD/FTDDR Webinar: Gene Therapy in FTD – December 3, 2020

AFTD-FTDDR-Gene-therapy-2020-12-03_0

Watch the webinar!

Watch the webinar!

Gene therapy is showing promise for treating a wide range of diseases, and related clinical trials are emerging for FTD. To share information on familial FTD, gene therapy, and the role of persons with FTD gene mutations, the Association for Frontotemporal Degeneration and the FTD Disorders Registry are hosting an educational webinar on Thursday, December 3, 2020, beginning at 3:00 p.m. EST (12:00 p.m. PST).

Experts presenting will be Erik Roberson, M.D., Ph.D., a neurologist at the University of Alabama at Birmingham (UAB) and director of the UAB Alzheimer’s Disease Center and the Center for Neurodegeneration and Experimental Therapeutics, and Olga Uspenskaya, M.D., Ph.D., a neurologist who serves as Vice President, Clinical Development at Prevail Therapeutics.

This webinar is part of “Perspectives in FTD Research,” a series of webinars conducted in partnership between AFTD and the FTD Registry. It will be hosted on AFTD’s platform and facilitated by Registry Director Dianna Wheaton, M.S., Ph.D., CHES.

Watch the replay below!

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Dr. Uspenskaya

Dr. Uspenskaya is a neurologist and serves at Prevail Therapeutics as Vice President, Clinical Development. Prior to joining Prevail Therapeutics, she served as senior medical director at IQVIA where she was responsible for the medical strategy of the neurology portfolio and was overseeing the execution of CNS clinical trials across different stages of clinical development.

Dr. Uspenskaya earned her M.D. and completed a residency in neurology at the First Moscow State Medical University. Subsequently, she completed a Ph.D. program in neurosciences at First Moscow State Medical University and Ludwig-Maximilians University, Munich, Germany; and a postdoctoral fellowship at the Sorbonne University Hospital Pitié-Salpêtrière, Paris, France. Her research was mainly on understanding of early phases of Alzheimer’s disease and validation of clinical biomarkers of neurodegeneration.

During her clinical and research career, Dr. Uspenskaya held academic positions which included research grants and lecturing on neurology topics. She has published in peer-reviewed clinical related journals, contributed to chapters in neurology textbooks, and presented at neurology conferences worldwide.

Dr. Roberson

Dr. Roberson is a physician-scientist dedicated to reducing the impact of age-related cognitive impairment. The Roberson Lab studies the neurobiology of Alzheimer’s disease (AD) and frontotemporal dementia (FTD), with a focus on understanding the cellular and molecular mechanisms of these disorders and identifying new therapeutic strategies. Focus areas include tau and its binding partners in neuronal dysfunction in AD, the mechanisms by which genetic risk factors drive AD, and how progranulin deficiency causes FTD.

Dr. Roberson received his A.B. with highest honors from Princeton University and then earned his M.D. and Ph.D. in neuroscience at Baylor College of Medicine where he studied molecular mechanisms of learning and memory. He completed a residency in neurology at the University of California San Francisco, where he also served as Chief Resident in Neurology. After residency, he completed a clinical fellowship in behavioral neurology with Dr. Bruce Miller at UCSF and resumed basic research in the laboratory of Dr. Lennart Mucke at the Gladstone Institute of Neurological Disease, initiating his current studies of neurodegenerative disease using mouse models. He joined the neurology faculty at UAB in 2008.

In addition to directing his laboratory, Dr. Roberson directs the UAB Alzheimer’s Disease Center and the Center for Neurodegeneration and Experimental Therapeutics. Dr. Roberson also cares for patients with memory disorders and dementia at the Kirklin Clinic and directs clinical trials related to tauopathies.

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The FTD Disorders Registry is a powerful tool in the movement to create therapies and find a cure. Together we can help change the course of the disease and put an end to FTD.

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