Search

Author/Creator Ferrie, Colin D.

1. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. (16th January 2015)

Authors:
Crow, Yanick J.; Chase, Diana S.; Lowenstein Schmidt, Johanna; Szynkiewicz, Marcin; Forte, Gabriella M.A.; Gornall, Hannah L.; Oojageer, Anthony; Anderson, Beverley; Pizzino, Amy; Helman, Guy; Abdel‐Hamid, Mohamed S.; Abdel‐Salam, Ghada M.; Ackroyd, Sam; Aeby, Alec; Agosta, Guillermo; Albin, Cath...
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 2(2015:Feb.)
Page Start:
296
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Pre-surgical mapping of eloquent cortex for paediatric epilepsy surgery candidates: Evidence from a review of advanced functional neuroimaging. (November 2017)

Authors:
Collinge, Sarah; Prendergast, Garreth; Mayers, Steven T.; Marshall, David; Siddell, Poppy; Neilly, Elizabeth; Ferrie, Colin D.; Vadlamani, Gayatri; Macmullen-Price, Jeremy; Warren, Daniel J.; Zaman, Arshad; Chumas, Paul; Goodden, John; Morrall, Matthew C.H.J.
Journal:
Seizure
Issue:
Volume 52(2017)
Page Start:
136
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search