Picacod 2024-Adrj436 - The Contribution Of Genetics In Epileptic And Developmental Encephalopat[...]
Organisation/Company: UNIMORE
Research Field: Medical sciences
Researcher Profile: Recognised Researcher (R2), Leading Researcher (R4), First Stage Researcher (R1), Established Researcher (R3)
Country: Italy
Application Deadline: 30 Jan 2025 - 13:00 (UTC)
Type of Contract: To be defined
Job Status: Not Applicable
Is the job funded through the EU Research Framework Programme? Not funded by a EU programme
Is the Job related to staff position within a Research Infrastructure? No
Offer DescriptionThe role of genetics in epilepsies is crucial today and is an investigation performed by clinical practice in pediatric patient populations suffering from severe epilepsy (DEE - Developmental and Epileptic Encephalopathies).
This diagnostic opportunity can also be offered to adolescent or adult patients who were unable to receive adequate genetic testing during childhood.
It is important to phenotypically characterize adult patients diagnosed with genetic epilepsies as the clinical and EEG features of the disease evolve with growth, and new phenotypes can characterize the disease picture in adulthood compared to childhood.
This project aims to phenotype adult patients with a genetic diagnosis in the EEG spectrum.
Eligibility of fellowsCountry/ies of residence: OTHER
Nationality/ies: OTHER
Selection processSelective public procedure by qualifications and interview.
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