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Browsing by Project Solve-RD
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model | Ruizhi Deng; Eva Medico-Salsench; Anita Nikoncuk; Reshmi Ramakrishnan; Kristina Lanko; Nikolas A Kühn; ... et al; Ivan Čapo   ; (broj, koautora 52) | Article | 21a+M21a+ |
| 2025 | Expanding the Genetic and Phenotypic Spectrum of DYT-VPS16: The Importance of Splice-Site Variants | Westenberger, Ana; ...; Cuturilo, Goran; ...; (broj, koautora 40) | Article | 21a+M21a+ |
| 2025 | Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models | Tedesco, Barbara; Perić, Stojan ; ...; Rakočević-Stojanović, Vidosava ; Milenković, Sanja ; ...; Ivanović, Vukan ; ...; (broj koautora 23) | Article | 21M21 |