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JAMA Neurology|December 3, 2019
Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical TrialRima Nabbout, Arun Mistry, Sameer Zuberi, et al.
Pediatric Diabetes|June 8, 2020
Psychological care in children and adolescents with type 1 diabetes in a real-world setting and associations with metabolic controlAngela Galler, Dörte Hilgard, Esther Bollow, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 28, 2023
Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotypeEllen Knierim, Johannes Vogt, Michael Kintscher, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2012
Structure of a hepatitis C virus RNA domain in complex with a translation inhibitor reveals a binding mode reminiscent of riboswitchesSergey M Dibrov, Kejia Ding, Nicholas D Brunn, et al.
Plos Genetics|May 27, 2010
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsiesHeather C Mefford, Hiltrud Muhle, Philipp Ostertag, et al.
Epilepsia|April 14, 2010
Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic regionConstanze Reutlinger, Ingo Helbig, Barbara Gawelczyk, et al.
Seizure|April 21, 2019
Quality of life and correlating factors in children, adolescents with epilepsy, and their caregivers: A cross-sectional multicenter study from GermanyJanna Riechmann, Laurent M Willems, Rainer Boor, et al.
Genesis (New York, N.Y. : 2000)|March 30, 2004
A reliable lacZ expression reporter cassette for multipurpose, knockout-first allelesGiuseppe Testa, Julia Schaft, Frank van der Hoeven, et al.
Bioorganic & Medicinal Chemistry Letters|April 29, 2008
Antibacterial activity in serum of the 3,5-diamino-piperidine translation inhibitorsYuefen Zhou, Chun Chow, Douglas E Murphy, et al.
Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, et al.
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