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- IRMS - Nicolae Testemitanu SUMPh
Browsing by Author Sacara, Victoria
Showing results 1 to 16 of 16
| Issue Date | Title | Author(s) | | 2021 | Analysis of clinical and molecular genetic characteristics of Wiskott-Aldrich syndrome and X-linked thrombocytopenia | Turcan, Doina; Andrieș, Lucia; Dorif, Alexandr; Sacara, Victoria |
| 2022 | Appreciation of short repeats number in neurogenetic disorders diagnostic | Dorif, Alexandr; Sacara, Victoria |
| 2021 | Cardiomyopathy secondary to Duchenne muscular dystrophy in children | Rodoman, Iulia; Palii, Ina; Sacara, Victoria; Gladun, Sergiu |
| 2020 | Challenging diagnosis: coexistence of two rare diseases – familial mediterranean fever and Loyez-Dietz syndrome type 3 | Revenco, Ninel; Andrieș, Lucia; Sacara, Victoria; Dorif, Alexandr; Barba, Doina; Eremciuc, Rodica; Gaidarji, Olga |
| 2021 | Collagen VI related muscle disorder. Ullrich congenital muscular dystrophy. Case report | Sacara, Victoria; Dorif, Alexandr; Usurelu, Natalia; Holling, Tese; Kubisch, Christian |
| 2025 | Congenital disorders of glycosylation - new considerations in the approach to the multisystem affected child | Blăniță, Daniela; Boiciuc, Chiril; Sacara, Victoria; Stamati, Adela; Hadjiu, Svetlana; Turea, Valentin; Nicolescu, Alina; Morava, Eva; Gladun, Sergiu; Ușurelu, Natalia |
| 2022 | Exchangeable copper - a new diagnostic indicator for Wilson's disease | Cumpata, Veronica; Sacara, Victoria; Turcanu, Adela |
| 2021 | First manifestation and evolution of early left ventricular dysfunction in children with Duchenne muscular dystrophy | Rodoman, Iulia; Dorif, Alexandr; Palii, Ina; Sacara, Victoria |
| 2013 | The functional activity of CHO cell lines expressing different ATP7B mutations (The cytotoxicity of the certain concentrations of Copper and Zinc) | Sacara, Victoria; Zibert, A.; Schmidt, H. H.-J. |
| 2012 | Genetic analysis of dystrophin gene in affected males and females carriers with Duchenne/Becker muscular dystrophy in Republic of Moldova between 1992 and 2012 | Sacara, Victoria |
| 2025 | De la imunodeficiențele primare la patologia cardiovasculară: punți între imunologie și cardiologie pediatrică | Palii, Ina; Sacara, Victoria; Pîrțu, Lucia; Eșanu, Veronica; Rodoman, Iulia; Ciuhrii, Olga |
| 2022 | Molecular genetic diagnosis of primary immunodeficiencies in the Republic of Moldova | Sacara, Victoria |
| 2016 | Rolul consultului medico-genetic în profilaxia bolilor genetice prin diagnostic citogenetic prenatal | Sprincean, Mariana; Barbova, Natalia; Uşurelu, Natalia; Halabudenco, Elena; Eţco, Ludmila; Secrieru, Viorica; Nour, Veronica; Sacara, Victoria; Stratila, M. |
| 2021 | The screening by isoelectric focusing of transferrin for the diagnosis of congenital disorders of glycosylation | Blăniță, Daniela; Boiciuc, Chiril; Țurcan, Doina; Sacara, Victoria; Ușurelu, Natalia |
| 2012 | Spectrul nozologic al bolilor ereditare ale sistemului nervos şi particularităţile răspîndirii patologiilor neuro-musculare în Republica Moldova | Sacara, Victoria; Leviţchi, Al.; Groppa, St.; Duca, Maria; Moşin, V. |
| 2022 | Wiskott-Aldrich syndrome at children - diagnostic particularities | Dorif, Alexandr; Secu, Doina; Sacara, Victoria |
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