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- IRMS - Nicolae Testemitanu SUMPh
Browsing by Author Boiciuc, Chiril
Showing results 1 to 15 of 15
| Issue Date | Title | Author(s) | | 2021 | Amino acids profile in the diagnosis of inborn errors of metabolism | Hlistun, Victoria; Efremov, Egor; Blanita, Daniela; Boiciuc, Chiril; Munteanu, Diana; Lupu, Victoria; Oglinda, Ana; Casian, Ana; Casian, Igor; Nicolescu, Alina; Deleanu, Calin; Usurelu, Natalia |
| 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 |
| 2020 | Challenges in clinical considerations for congenital disorders of glycosylation | Blăniță, Daniela; Boiciuc, Chiril; Samohvalov, Elena; Sacară, Victoria; Barbova, Natalia; Hadjiu, Svetlana; Țurea, Valentin; Stamati, Adela; Nicolescu, Alina; Deleanu, Calin; Lefeber, Dirk; Morava, Eva; Ușurelu, Natalia |
| 2021 | Classical galactosemia - a case report | Scurtul, Maria; Boiciuc, Chiril; Blăniță, Daniela; Sacară, Victoria; Tarcomnicu, Isabela; Stambouli, Danae; Nicolescu, Alina; Deleanu, Calin; Gladun, Sergiu; Ușurelu, Natalia |
| 2020 | Complexity of the diagnosis of Congenital Disorders of Glycosylation | Blăniță, Daniela; Boiciuc, Chiril; Țurea, Valentin; Stamati, Adela; Morava, Eva; Ușurelu, Natalia |
| 2020-10 | Complexity of the diagnosis of congenital disorders of glycosylation | Blăniță, Daniela; Boiciuc, Chiril; Țurea, Valentin; Stamati, Adela; Morava, Eva; Ușurelu, Natalia |
| 2020 | Diagnosis characteristics of congenital disorders of glycosylation of 40 suspected patients from Moldova | Boiciuc, Chiril; Blăniță, Daniela; Samohvalov, Elena; Tagadiuc, Olga; Nicolescu, Alina; Deleanu, Călin; Wevers, Ron; Huijben, Karin; Lefeber, Dirk; Ușurelu, Natalia |
| 2021 | The importance of plasma amino acid profile in the diagnosis of inboorn errors of metabolism | Hlistun, Victoria; Efremov, Egor; Blăniță, Daniela; Boiciuc, Chiril; Ușurelu, Natalia |
| 2021 | The importance of plasma amino acid profiling in the diagnosis of inborn errors of metabolism | Hlistun, Victoria; Efremov, Egor; Blăniță, Daniela; Boiciuc, Chiril; Ușurelu, Natalia |
| 2022 | Importanța profilului aminoacizilor plasmatici în diagnosticul erorilor înnăscute de metabolism: studiu prospectiv, analitic | Hlistun, Victoria; Efremov, Egor; Blăniță, Daniela; Boiciuc, Chiril; Deleanu, Calin; Nicolescu, Alina; Ușurelu, Natalia |
| 2020 | Molecular genetics in Phenylketonuria in Republic of Moldova (2018- 2019) | Scurtul, Maria; Boiciuc, Chiril; Blăniță, Daniela; Croitori, Tamara; Lazari, Nicoleta |
| 2020 | Molecular genetics in phenylketonuria in Republic of Moldova (2018- 2019) | Scurtul, Maria; Boiciuc, Chiril; Blăniţă, Daniela; Croitori, Tamara; Lazari, Nicoleta; Uşurelu, Natalia |
| 2020 | Phenotype prediction in phenylketonuria patients from Moldova based on genotype data | Scurtul, Maria; Boiciuc, Chiril; Blăniță, Daniela; Sacară, Victoria; Ușurelu, Natalia |
| 2021 | The screening by isoelectric focusing of transferrin for the diagnosis of congenital disorders of glycosylation | Blanita, Daniela; Boiciuc, Chiril; Turcan, Doina; Sacara, Victoria; Usurelu, Natalia |
| 2021 | The screening of congenital disorders of glycosylation by isoelectrofocusing of transferrine | Blăniță, Daniela; Boiciuc, Chiril; Morava, Eva; Lefeber, Dirk; Ușurelu, Natalia |
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