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Bryan Woodruff

Showing results (1-10 of 4) with videos related to

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American Journal of Medical Genetics. Part A|April 30, 2015
High functioning male with fragile X syndrome and fragile X-associated tremor/ataxia syndromeKirin Basuta, Andrea Schneider, Louise Gane, et al.
Molecular Autism|February 19, 2026
Association of glymphatic dysfunction, free water, white matter integrity and long-term memory performance in aging autistic adultsYuanchao Zhang, Edward Ofori, Kewei Chen, et al.
Archives of Neurology|February 16, 2006
Steroid-responsive encephalopathy associated with autoimmune thyroiditisPablo Castillo, Bryan Woodruff, Richard Caselli, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|April 30, 2015
High functioning male with fragile X syndrome and fragile X-associated tremor/ataxia syndromeKirin Basuta, Andrea Schneider, Louise Gane, et al.
Molecular Autism|February 19, 2026
Association of glymphatic dysfunction, free water, white matter integrity and long-term memory performance in aging autistic adultsYuanchao Zhang, Edward Ofori, Kewei Chen, et al.
Archives of Neurology|February 16, 2006
Steroid-responsive encephalopathy associated with autoimmune thyroiditisPablo Castillo, Bryan Woodruff, Richard Caselli, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
Pageof 1