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Browsing by Author Ușurelu, Natalia

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Showing results 13 to 32 of 32 < previous 
Issue DateTitleAuthor(s)
2021The importance of plasma amino acid profile in the diagnosis of inboorn errors of metabolismHlistun, Victoria; Efremov, Egor; Blăniță, Daniela; Boiciuc, Chiril; Ușurelu, Natalia
2021The importance of plasma amino acid profiling in the diagnosis of inborn errors of metabolismHlistun, Victoria; Efremov, Egor; Blăniță, Daniela; Boiciuc, Chiril; Ușurelu, Natalia
2022Importanța profilului aminoacizilor plasmatici în diagnosticul erorilor înnăscute de metabolism: studiu prospectiv, analiticHlistun, Victoria; Efremov, Egor; Blăniță, Daniela; Boiciuc, Chiril; Deleanu, Calin; Nicolescu, Alina; Ușurelu, Natalia
2020Introduction into inborn errors of metabolismUșurelu, Natalia
2021Leigh syndrome: a rare case reportȚurcan, Doina; Ușurelu, Natalia; Blăniță, Daniela; Sacară, Victoria
2021Leigh syndrome: a rare case reportȚurcan, Doina; Ușurelu, Natalia; Blăniță, Daniela; Sacară, Victoria
2021The metabolic impact of primary childhood obesityMunteanu, Diana; Hlistin, Victoria; Rizov, Cristina; Vudu, Lorina; Ușurelu, Natalia
2020Methodological approaches in the molecular genetic analysis of mitochondrial DNA in patients with common clinical features of mitochondrial diseaseȚurcan, Doina; Blăniță, Daniela; Ușurelu, Natalia; Sacară, Victoria
2023Modificările profilului aminoacizilor cu lanț ramificat în obezitatea primară la copii și adolescențiMunteanu, Diana; Ușurelu, Natalia; Vudu, Lorina
2021Multisystem 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
2020Nonketotic hyperglycinemia – case reportHlistun, Victoria; Blăniță, Daniela; Lupu, Victoria; Golub, Natalia; Oglinda, Ana; Garaeva, Svetlana; Postolati, Galina; Tarcomnicu, Isabela; Stambouli, Danae; Nicolescu, Alina; Deleanu, Calin; Ușurelu, Natalia
2020Phenotype prediction in phenylketonuria patients from Moldova based on genotype dataScurtul, Maria; Boiciuc, Chiril; Blăniță, Daniela; Sacară, Victoria; Ușurelu, Natalia
2021A rare mitochondrial disorder: Leigh syndrome – a case reportȚurcan, Doina; Ușurelu, Natalia; Blăniță, Daniela; Sacară, Victoria
2021The screening of congenital disorders of glycosylation by isoelectrofocusing of transferrineBlăniță, Daniela; Boiciuc, Chiril; Morava, Eva; Lefeber, Dirk; Ușurelu, Natalia
2020Spinal muscular atrophy: news and perspectivesColiban, Iulia; Revenco, Ninel; Țurcan, Doina; Egorov, Vladimir; Ușurelu, Natalia; Sacară, Victoria
2023Strategii de testare moleculară ale maladiilor mitocondriale cauzate de mutațiile ADN-ului mitocondrialSecu, Doina; Ușurelu, Natalia; Blăniță, Daniela; Dorif, Alexandr; Sacară, Victoria
2020Syndromal dislipidemia - case report of a family with Alstrom syndromeMunteanu, Diana; Hlistun, Victoria; Samohvalov, Elena; Blăniță, Daniela; Stamati, Adela; Vudu, Lorina; Ușurelu, Natalia
2021Unbalanced genomic changes and SMA? : case reportColiban, Iulia; Blăniță, Daniela; Egorov, Vladimir; Halabudenco, Elena; Sacară, Victoria; Ușurelu, Natalia
2021Unbalanced genomic changes and SMA? Case reportColiban, Iulia; Egorov, Vladimir; Sacară, Victoria; Ușurelu, Natalia
2021X-Linked Adrenoleukodystrophy in Republic of Moldova: case reportBlăniță, Daniela; Sacară, Victoria; Railean, Gheorghe; Stamati, Adela; Garaeva, Svetlana; Postolachi, Galina; Hoffmann, George Franz; Steinfeld, Robert; Ușurelu, Natalia

 

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