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European Journal of Human Genetics : EJHG|April 5, 2007
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridiaR Alex Henderson, Kathy Williamson, Sally Cumming, et al.
International Journal of Audiology|April 25, 2007
Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutationDoris-Eva Bamiou, Nicole G Campbell, Frank E Musiek, et al.
Neurology|July 8, 2016
Value of patient-reported symptoms in the diagnosis of transient loss of consciousnessMarkus Reuber, Min Chen, Jenny Jamnadas-Khoda, et al.
Neurology. Clinical Practice|April 21, 2020
Machine learning as a diagnostic decision aid for patients with transient loss of consciousnessAlistair Wardrope, Jenny Jamnadas-Khoda, Mark Broadhurst, et al.
The Journal of Biological Chemistry|October 18, 2007
Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumptionMatthew McKenzie, Danae Liolitsa, Natalya Akinshina, et al.
Human Genetics|June 4, 2014
Opposite effects on facial morphology due to gene dosage sensitivityPeter Hammond, Shane McKee, Michael Suttie, et al.
Epilepsia|September 10, 2024
N-of-1 trials in epilepsy: A systematic review and lessons paving the way forwardVictoria M Defelippe, Eva H Brilstra, Willem M Otte, et al.
Human Brain Mapping|June 20, 2012
Imaging the interaction: epileptic discharges, working memory, and behaviorUmair J Chaudhary, Maria Centeno, David W Carmichael, et al.
Brain Pathology (Zurich, Switzerland)|April 6, 2017
Characterising subtypes of hippocampal sclerosis and reorganization: correlation with pre and postoperative memory deficitAnaclara Prada Jardim, Joan Liu, Jack Baber, et al.
Epilepsia|May 23, 2013
International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: a Task Force report from the ILAE Commission on Diagnostic MethodsIngmar Blümcke, Maria Thom, Eleonora Aronica, et al.
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