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pro vyhledávání: '"Megan Baird"'
Autor:
Maura Schwartz, Alex Campbell, Joseph Caporale, Megan Baird, Isabella Palazzo, Shibi Likhite, Andrew Fischer, Kathrin Meyer
Publikováno v:
Proceedings, Vol 71, Iss 1, p 5 (2020)
Batten Disease is a fatal lysosomal storage disorder characterized by cognitive and [...]
Externí odkaz:
https://doaj.org/article/5232a16d91ed4005a9ad94e87c7e1d51
Autor:
Maura Schwartz, Alex Campbell, Joseph Caporale, Megan Baird, Isabella Palazzo, Shibi Likhite, Andrew Fischer, Kathrin Meyer
Publikováno v:
Proceedings, Vol 71, Iss 5, p 5 (2021)
NEDAMSS is a newly discovered neurodevelopmental disorder with regression, abnormal movements, loss of speech and seizures. The disease is caused by heterozygous mutations in the Interferon Regulatory Factor 2 Binding Protein-Like (IRF2BPL) gene. IRF
Autor:
Megan Baird
Publikováno v:
Current Trends in Clinical & Medical Sciences. 2
Autor:
Eric C. Bielefeld, Maura Schwartz, Megan Baird, Ronald M. Lindsay, Shibi Likhite, Jia Xie, Marie-Anne Colle, Kathrin Meyer, Lynne Bianchi, Karim Bey, Ricardo J. Pineda, Peter S. DiStefano
Publikováno v:
Proceedings of 1st International Electronic Conference on Brain Sciences.
Noise-induced hearing loss (NIHL) is one of the most prevalent disabilities for which effective therapeutic treatment is currently lacking. Auditory injury caused by excessive or constant noise exposure damages the sensory elements of the ear, leadin
Autor:
Alex Campbell, Joseph Caporale, Shibi Likhite, Kathrin Meyer, Megan Baird, Maura Schwartz, Isabella Palazzo, Andy J. Fischer
Publikováno v:
Proceedings of 1st International Electronic Conference on Brain Sciences.
Batten Disease is a fatal, lysosomal storage disorder characterized by cognitive and motor deficits, vision impairments, and seizures. Loss of vision is a hallmark of 10 of the 13 Batten Disease subtypes. Our group has pioneered AAV9 gene therapy tre