Article
Delineation of the movement disorders associated with FOXG1 mutations.
Neurology - 10 May 2016
Papandreou Apostolos, Schneider Ruth B, Augustine Erika F, Ng Joanne, Mankad Kshitij, Meyer Esther, McTague Amy, Ngoh Adeline, Hemingway Cheryl, Robinson Robert, Varadkar Sophia M, Kinali Maria, Salpietro Vincenzo, O'Driscoll Margaret C, Basheer S Nigel, Webster Richard I, Mohammad Shekeeb S, Pula Shpresa, McGowan Marian, Trump Natalie, Jenkins Lucy, Elmslie Frances, Scott Richard H, Hurst Jane A, Perez-Duenas Belen, Paciorkowski Alexander R, Kurian Manju A
Abstract excerpt
OBJECTIVE: The primary objective of this research was to characterize the movement disorders associated with FOXG1 mutations. METHODS: We identified patients with FOXG1 mutations who were referred to either a tertiary movement disorder clinic or tertiary epilepsy service and retrospectively reviewed medical records, clinical investigations, neuroimaging, and available video footage. We administered a...
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