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Uncinate Epilepsy: Disease Bioinformatics
Epilepsy is defined as a diverse set of neurological disorders characterized by seizures. These seizures occur due to abnormal electrical activity in the brain. Factors that may lead to epilepsy include, but are not limited to, brain trauma, gene mutations, strokes, brain cancer, and extensive drug and alcohol use. Seizures occur due to a large release of glutamate, which causes a spread of excitation throughout the brain, which propagates the electrical signal and can lead to neuronal death. Uncinate epilepsy is a form of psychomotor epilepsy that is initiated by a dreamy state and by hallucinations of smell and taste. Uncinate epilepsy is usually caused by a medial temporal lesion. About 50 million people have epilepsy, with 80% of that population located in developing countries. It is possible to control epilepsy with medicine, but many cases may require surgery in order to relieve symptoms.
Uncinate Epilepsy Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Uncinate Epilepsy below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
We have 168 products for the study of Uncinate Epilepsy that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Applications WB, IHC, IHC-P
Uncinate Epilepsy has been researched against:
Uncinate Epilepsy has been linked to:
Uncinate Epilepsy has been studied in relation to diseases such as:
Alternate NamesUncinate Epilepsy is also known as Uncinate Fits.