PARALLEL SESSION 1B: Neurogenetics I
Tracks
SKALKOTAS HALL
| Wednesday, September 18, 2019 |
| 10:30 AM - 12:15 PM |
| SKALKOTAS HALL |
Speaker
Prof. Holger Prokisch
Institute of Human Genetics, Technical University Munich
Neurogenetics: Diagnostics – Introduction on NBIAs
10:30 AM - 10:55 AM
Dr. Dina Amrom
Hôpital Des Enfants Reine Fabiola
OC006 | Clinical, radiological and genetic findings in a cohort of 65 Polymicrogyria patients
10:55 AM - 11:10 AM
Dr. Bülent Kara
Kocaeli University Medical Faculty
OC007 | A new neurodegenerative disorder characterized with cystic pontine degeneration and cerebellar atrophy due to BEND4 gene mutation
11:10 AM - 11:25 AM
Dr. Walid Fazeli
University Children's Hospital Cologne, Germany
OC008 | Clinical and genetic spectrum of SCN2A-associated episodic Ataxia
11:25 AM - 11:40 AM
Dr. Hanna Hulshof
UMC Utrecht
OC009 | Neuroimaging findings as biomarkers of epilepsy risk and neurodevelopment at two years in patients with Tuberous Sclerosis Complex (TSC)
11:40 AM - 11:55 AM
Dr. Yuqing Shi
Beijing Children's Hospital
OC010 | 176 cases of mitochondrial diseases with mitochondrial DNA variations in Chinese children
11:55 AM - 12:10 PM
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Discussion
12:10 PM - 12:15 PMChair
Andreas Brunklaus
Paediatric Neurosciences Research Group, Royal Hospital For Children, Glasgow
Artemis Gika
University of Athens, Aghia Sophia Children's Hospital
