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Nature Genetics|April 2, 2013
Mutations of DEPDC5 cause autosomal dominant focal epilepsiesSaeko Ishida, Fabienne Picard, Gabrielle Rudolf, et al.
Annals of Clinical and Translational Neurology|March 9, 2019
Mild malformations of cortical development in sleep-related hypermotor epilepsy due to KCNT1 mutationsGuido Rubboli, Giuseppe Plazzi, Fabienne Picard, et al.
Swiss Medical Weekly|December 31, 2020
Early experimental COVID-19 therapies: associations with length of hospital stay, mortality and related costsNathalie Vernaz, Thomas Agoritsas, Alexandra Calmy, et al.
Neurobiology of Aging|July 15, 2020
Gray matter changes related to microglial activation in Alzheimer's diseaseNicolas Nicastro, Maura Malpetti, Elijah Mak, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|November 1, 2019
Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical featuresAudrey Low, Elijah Mak, Maura Malpetti, et al.
Epilepsy Research|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Brain Communications|September 6, 2021
[18F]-AV-1451 binding in the substantia nigra as a marker of neuromelanin in Lewy body diseasesElijah Mak, Antonina Kouli, Negin Holland, et al.
Annals of Neurology|January 28, 2015
Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutationsStéphanie Baulac, Saeko Ishida, Elise Marsan, et al.
Neuroimage. Clinical|February 8, 2020
Correlation of microglial activation with white matter changes in dementia with Lewy bodiesNicolas Nicastro, Elijah Mak, Guy B Williams, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
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