Inhalt

[ 405ERSLTGCK25 ] KS Translation in the area of genetically caused developmental delays with and without epilepsy

Versionsauswahl
(*) Unfortunately this information is not available in english.
Workload Education level Study areas Responsible person Hours per week Coordinating university
1 ECTS R - Doctoral programme Human Medicine Gudrun Gröppel 1 hpw Johannes Kepler University Linz
Detailed information
Pre-requisites (*)Doktoratsstudium Doctoral Program in Medical Sciences
Original study plan Doctoral programme Medical Sciences 2025W
Learning Outcomes
Competences
Students can identify clinical questions that can be addressed through genetic diagnostics and basic scientific approaches, bridging clinical practice with translational research.
Skills Knowledge
  • Recognizing clinical questions suitable for genetic diagnostics.
  • Applying genetic analysis to answer medical research questions.
  • Understanding the connection between clinical practice and scientific principles.
  • Exploring emerging concepts in gene therapy.
  • Fundamentals of genetic diagnostics in clinical settings.
  • The role of translational science in medicine.
  • Integration of genetic insights into patient care.
  • Future developments and applications of gene therapy.
Criteria for evaluation Attendance of at least 80 %

At the end of the course, the results should be presented to the group. This gives the course an immanent examination character.

Methods Interactive lectures
Language English
Changing subject? No
Further information The course is conducted together with colleagues from the Institute of Genetics and the Research Laboratory.
On-site course
Maximum number of participants 15
Assignment procedure Assignment according to priority