| 1 |
Global Myoclonus Dystonia registry and non-motor symptoms study |
| 2 |
Natural History in ATP1A3-related disease: a deep phenotyping - genotyping |
| 3 |
Developmental Spectrum of Presynaptic Genetic Disorders: STXBP1, PRRT2, DNM1, SYT1 |
| 4 |
Neurological complications of COVID-19 |