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Ideggyogyaszati Szemle|June 12, 2018
[Nusinersen in the treatment of spinal muscular atrophy]Gabriella Sinkó, Zsuzsanna Kiss, Bernadette Kalman
Orvosi Hetilap|February 23, 2025
[Duplication of the X-chromosomal Xq28 region containing the MECP2 gene in X-linked intellectual disability syndrome Lubs-type]Zsófia Németh, Gabriella Sinkó, Judit Kárteszi, et al.
Ideggyogyaszati Szemle|June 3, 2024
[Vanishing white matter disease, a rare leukodystrophy with mutation in the EIF2B5 gene]Gabriella Sinkó, Márton Tompa, Zsuzsanna Kiss, et al.
Ideggyogyaszati Szemle|August 5, 2026
Globoid cell leukodystrophy (Krabbe disease)Gabriella Sinkó, Eszter Dénes, Gábor Farkas, et al.
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