YAHYA, VIDAL
YAHYA, VIDAL
Universita' degli Studi di MILANO
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Risultati 1 - 3 di 3 (tempo di esecuzione: 0.0 secondi).
Genetic Evidence for Endolysosomal Dysfunction in Parkinson’s Disease: A Critical Overview
2023 V. Yahya, A. Di Fonzo, E. Monfrini
GABRB1‐related early onset developmental and epileptic encephalopathy: Clinical trajectory and novel de novo mutation
2023 E. Monfrini, L. Borellini, E. Zirone, V. Yahya, E. Mauri, M.T. Molisso, F. Mameli, F. Ruggiero, G.P. Comi, S. Barbieri, Di , A. Fonzo, R. Dilena
Juvenile-onset dystonia with spasticity in Leigh syndrome caused by a novel NDUFA10 variant
2022 V. Yahya, F. Spagnolo, G. Di Maggio, E. Leopizzi, P. De Marco, F. Fortunato, G.P. Comi, A. Rini, E. Monfrini, A. Di Fonzo
Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
---|---|---|---|---|---|
Genetic Evidence for Endolysosomal Dysfunction in Parkinson’s Disease: A Critical Overview | 2023 | Yahya V.Monfrini E. + | Article (author) | - | |
GABRB1‐related early onset developmental and epileptic encephalopathy: Clinical trajectory and novel de novo mutation | 2023 | Monfrini, EdoardoBorellini, LindaYahya, VidalMameli, FrancescaComi, Giacomo Pietro + | Article (author) | - | |
Juvenile-onset dystonia with spasticity in Leigh syndrome caused by a novel NDUFA10 variant | 2022 | Yahya, VidalDe Marco, PaoloFortunato, FrancescoComi, Giacomo PMonfrini, Edoardo + | Article (author) | - |