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Identification of genetic loci for human epilepsies

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dc.contributor.advisor Anand, Anuranjan
dc.contributor.author Ratnapriya, R.
dc.date.accessioned 2012-09-07T11:31:48Z
dc.date.available 2012-09-07T11:31:48Z
dc.date.issued 2009
dc.identifier.citation Ratnapriya, R. 2009, Identification of genetic loci for human epilepsies, Ph.D thesis, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru en_US
dc.identifier.uri https://libjncir.jncasr.ac.in/xmlui/10572/813
dc.description Open access
dc.description.abstract Epilepsy is relatively common neurological disorder affecting 0.5-1% of population during their lifetime (Hauser et al., 1993; Kaneko et al., 2002). Epilepsy is characterized by usually unprovoked and recurrent seizures, which are consequence of intensive burst activity from groups of neurons. Epileptic seizures are usually intermittent, self-limiting and occur with or without loss of consciousness. Seizures are generalized when synchronized firing of neurons involves the whole brain, or focal wherein seizure activity is limited to a specific brain region. While final outcome of seizure results from many complex and interacting biological phenomenon, abnormal cellular excitability and neuronal network defects are considered the two major physiological elements underlying seizure activity of the brain.
dc.language.iso English en_US
dc.publisher Jawaharlal Nehru Centre for Advanced Scientific Research en_US
dc.rights © 2009 JNCASR en_US
dc.subject Human Epilepsies en_US
dc.subject Molecular Biology en_US
dc.title Identification of genetic loci for human epilepsies en_US
dc.type Thesis en_US
dc.type.qualificationlevel Doctoral en_US
dc.type.qualificationname Ph.D. en_US
dc.publisher.department Molecular Biology and Genetics Unit (MBGU) en_US


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