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- IRMS - Nicolae Testemitanu SUMPh
Browsing by Author Țurcan, Doina
Showing results 1 to 7 of 7
| Issue Date | Title | Author(s) | | 2021 | The challenge in diagnosis of congenital disorders of glycosylation versus mitochondrial disorders: case report | Blăniță, Daniela; Boiciuc, Chiril; Țurcan, Doina; Sacară, Victoria; Țurea, Valentin; Stamati, Adela; Hadjiu, Svetlana; Lefeber, Dirk; Morava, Eva; Ușurelu, Natalia |
| 2021 | Leigh syndrome: a rare case report | Țurcan, Doina; Ușurelu, Natalia; Blăniță, Daniela; Sacară, Victoria |
| 2021 | Leigh syndrome: a rare case report | Țurcan, Doina; Ușurelu, Natalia; Blăniță, Daniela; Sacară, Victoria |
| 2020 | Methodological approaches in the molecular genetic analysis of mitochondrial DNA in patients with common clinical features of mitochondrial disease | Țurcan, Doina; Blăniță, Daniela; Ușurelu, Natalia; Sacară, Victoria |
| 2021 | Multisystem affection in child: NARP syndrome – mitochondrial disease (case presentation) | Blăniță, Daniela; Țurcan, Doina; Garaeva, Svetlana; Postolati, Galina; Sacară, Victoria; Wevers, Ron; Rodenburg, Richard; Ușurelu, Natalia |
| 2021 | A rare mitochondrial disorder: Leigh syndrome – a case report | Țurcan, Doina; Ușurelu, Natalia; Blăniță, Daniela; Sacară, Victoria |
| 2020 | Spinal muscular atrophy: news and perspectives | Coliban, Iulia; Revenco, Ninel; Țurcan, Doina; Egorov, Vladimir; Ușurelu, Natalia; Sacară, Victoria |
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