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Immunogenetics|December 3, 2017
Increased herpes zoster risk associated with poor HLA-A immediate early 62 protein (IE62) affinityPieter Meysman, Nicolas De Neuter, Esther Bartholomeus, et al.Neurology|May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsyFabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.Journal of Translational Medicine|August 25, 2019
Diagnosing enterovirus meningitis via blood transcriptomics: an alternative for lumbar puncture?Esther Bartholomeus, Nicolas De Neuter, Annelies Lemay, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 9, 2013
PRRT2 mutations: exploring the phenotypical boundariesTania Djémié, Sarah Weckhuysen, Philip Holmgren, et al.Neurology|March 14, 2014
GABRA1 and STXBP1: novel genetic causes of Dravet syndromeGemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, et al.Cell Reports|July 28, 2026
Blood transcriptome bridges orthogonal immunotypes and gut microbiome enterotypes in humansFabio Affaticati, My K Ha, Thies Gehrmann, et al.Brain : a Journal of Neurology|June 26, 2008
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1Arvid Suls, Peter Dedeken, Karolien Goffin, et al.Brain : a Journal of Neurology|September 20, 2015
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasiaKatia Hardies, Carolien G F de Kovel, Sarah Weckhuysen, et al.Molecular Genetics & Genomic Medicine|September 22, 2016
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patientsCarolien G F de Kovel, Eva H Brilstra, Marjan J A van Kempen, et al.Neurology|October 11, 2013
Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patientsSarah Weckhuysen, Vanja Ivanovic, Rik Hendrickx, et al.Pageof 7