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Neurology|December 31, 2017
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patientsMark McCormack, Hongsheng Gui, Andrés Ingason, et al.
Molecular Genetics & Genomic Medicine|July 29, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutationsTania Djémié, Sarah Weckhuysen, Sarah von Spiczak, et al.
Brain : a Journal of Neurology|March 19, 2015
CHD2 variants are a risk factor for photosensitivity in epilepsyElizabeth C Galizia, Candace T Myers, Costin Leu, et al.
Brain : a Journal of Neurology|September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, et al.
NPJ Parkinson'S Disease|April 20, 2026
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Nicole Kuznetsov, et al.
Neuropathology and Applied Neurobiology|August 13, 2021
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsiesAndre Altmann, Mina Ryten, Martina Di Nunzio, et al.
Biological Psychiatry|September 3, 2023
Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion CarriersRune Boen, Tobias Kaufmann, Dennis van der Meer, et al.
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