Epilepsy
What's New
Last Posted: Jul 15, 2024
- Clinical signatures of genetic epilepsies precede diagnosis in electronic medical records of 32,000 individuals
- A computational clinical decision-supporting system to suggest effective anti-epileptic drugs for pediatric epilepsy patients based on deep learning models using patient's medical history.
Daeahn Cho et al. BMC Med Inform Decis Mak 2024 24(1) 149 - Evaluating the Inheritance Risk: Epilepsy Prevalence among Offspring of Adults with Epilepsy in a Tertiary Referral Epilepsy Center.
Tassanai Intravooth et al. J Clin Med 2024 13(10) - Dementia in Rare Genetic Neurodevelopmental Disorders: A Systematic Literature Review.
Hadassa Kwetsie et al. Neurology 2024 102(11) e209413 - Economic Evaluation of HLA-B*15:02 Genotyping for Asian Australian Patients With Epilepsy.
Yaron Gu et al. JAMA Dermatol 2024 - Artificial intelligence in epilepsy - applications and pathways to the clinic.
Alfredo Lucas et al. Nat Rev Neurol 2024 - Reliable detection of generalized convulsive seizures using an off-the-shelf digital watch: A multisite phase 2 study.
Yash Shashank Vakilna et al. Epilepsia 2024 - Clinically significant changes in genes and variants associated with epilepsy over time: implications for re-analysis.
Alan J Robertson et al. Sci Rep 2024 14(1) 7717 - A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals.
Mariela V Jennings et al. EBioMedicine 2024 105086 - Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions.
Ali AlMail et al. NPJ Genom Med 2024 9(1) 27
More
About ND PHGKB
Neurological Disorders (ND) PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to neurological disorders....more
Content Summary
Common ND Related Topics
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Content source: