Browsing eNauka
Browsing by Project European Reference Network for Rare Neurological Disease
Showing results 1 to 2 of 2
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2022 | De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia | Van, de Vondel Liedewei; ...; Brankovic, Vesna; ...; (broj, koautora 38) | Article | 21a+M21a+ |
| 2022 | Tau deposition patterns are associated with functional connectivity in primary tauopathies | Franzmeier, Nicolai; ...; Lukic, Milica J; ...; (broj, koautora 60) | Article | 21a+M21a+ |