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- IRMS - Nicolae Testemitanu SUMPh
Browsing by Author Dorif, Alexandr
Showing results 1 to 9 of 9
| 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 |
| 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 |
| 2021 | First manifestation and evolution of early left ventricular dysfunction in children with Duchenne muscular dystrophy | Rodoman, Iulia; Dorif, Alexandr; Palii, Ina; Sacara, Victoria |
| 2020 | Ghid de conduită diagnostică şi tratament pentru imunodeficienţele primare combinate severe şi celulare | Andrieş, Lucia; Revenco, Ninel; Sacară, Victoria; Barbă, Doina; Ţurcanu, Tamara; Dorif, Alexandr; Chiveli, Veronica; Turcu, Oxana; Vişnevschi, Anatol |
| 2023 | Strategii de testare moleculară ale maladiilor mitocondriale cauzate de mutațiile ADN-ului mitocondrial | Secu, Doina; Ușurelu, Natalia; Blăniță, Daniela; Dorif, Alexandr; Sacară, Victoria |
| 2021 | Subclinical left ventricular dysfunction in children with Duchenne muscular dystrophy | Rodoman, Iulia; Pîrțu, Lucia; Dorif, Alexandr; Sacară, Victoria; Palii, Ina |
| 2022 | Wiskott-Aldrich syndrome at children - diagnostic particularities | Dorif, Alexandr; Secu, Doina; Sacara, Victoria |
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