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1Academic Journal
المؤلفون: TURCAN, Doina, ANDRIES, Lucia, DORIF, Alexandr, SACARA, Victoria
المصدر: One Health & Risk Management ; Vol. 2 No. 3 (2021); 61-66 ; Vol 2 Nr 3 (2021); 61-66 ; Том 2 № 3 (2021); 61-66 ; 2587-3466 ; 2587-3458
مصطلحات موضوعية: Wiskott Aldrich syndrome, Xlinked thrombocytopenia, immunodeficiency, syndrome de Wiskott-Aldrich, thrombocytopénie liées à l’X, immunodéficience, Синдром Вискотта-Олдрича, Х-сцепленная тромбоцитопения, иммунодефицит
وصف الملف: application/pdf
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2Academic Journal
المؤلفون: Turcan, Doina, Andrieș, Lucia, Dorif, Alexandr, Sacara, Victoria
مصطلحات موضوعية: Wiskott Aldrich syndrome, Xlinked thrombocytopenia, immunodeficiency, CZU: [616.155.294+612.017.1]-053.2:575.224
وصف الملف: application/pdf
Relation: One Health & Risk Management; https://doi.org/10/38045/ohrm.2021.3.10; http://repository.usmf.md/handle/20.500.12710/17882; https://journal.ohrm.bba.md/index.php/journal-ohrm-bba-md/article/view/141/99
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3Academic Journal
المؤلفون: Țurcan, Doina, Ușurelu, Natalia, Blăniță, Daniela, Sacară, Victoria
مصطلحات موضوعية: Leigh syndrome, mitochondrial DNA, mitochondrial disease
وصف الملف: application/pdf
Relation: Buletin de perinatologie; ȚURCAN, Doina, UȘURELU, Natalia, BLĂNIȚĂ, Daniela, SACARĂ, Victoria. A rare mitochondrial disorder: Leigh syndrome – a case report. In: Buletin de perinatologie. 2021, nr. 1(90), pp. 81-85. ISSN 1810-5289.; http://repository.usmf.md/./handle/20.500.12710/18215
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4Academic Journal
المؤلفون: Blăniță, Daniela, Țurcan, Doina, Garaeva, Svetlana, Postolati, Galina, Sacară, Victoria, Wevers, Ron, Rodenburg, Richard, Ușurelu, Natalia
مصطلحات موضوعية: NARP syndrome, multisystemic affectation, mitochondrial disease
وصف الملف: application/pdf
Relation: Buletin de perinatologie; BLĂNIȚĂ, Daniela, ȚURCAN, Doina, GARAEVA, Svetlana, et al. Multisystem affection in child: Narp syndrome – mitochondrial disease (case presentation). In: Buletin de perinatologie. 2021, nr. 1(90), pp. 86-91. ISSN 1810-5289.; http://repository.usmf.md/./handle/20.500.12710/18216
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5Academic Journal
مصطلحات موضوعية: congenital disorders of glycosylation, multisystem affections, isoelectric focusing of transferring, UDC: 616-008.9-053.1-07
وصف الملف: application/pdf
Relation: The Moldovan Medical Journal; BLANITA, Daniela, BOICIUC, Chiril, TURCAN, Doina, SACARA, Victoria, USURELU, Natalia. The screening by isoelectric focusing of transferrin for the diagnosis of congenital disorders of glycosylation. . In: The Moldovan Medical Journal. 2021, vol. 64, no 4, pp. 50-54. ISSN 2537-6381. https://doi.org/10.52418/moldovan-med-j.64-4.21.09; http://moldmedjournal.md/wp-content/uploads/2021/10/Moldovan-Med-J-Vol-64-No-4-vers-5.pdf; https://doi.org/10.52418/moldovan-med-j.64-4.21.09; http://repository.usmf.md/handle/20.500.12710/18190
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6Academic Journal
المؤلفون: Blăniță, Daniela, Boiciuc, Chiril, Țurcan, Doina, Sacară, Victoria, Țurea, Valentin, Stamati, Adela, Hadjiu, Svetlana, Lefeber, Dirk, Morava, Eva, Ușurelu, Natalia
مصطلحات موضوعية: CDG, Mds, IEFT, sequencing
وصف الملف: application/pdf
Relation: Buletin de perinatologie; BLĂNIȚĂ, Daniela, BOICIUC, Chiril, ȚURCAN, Doina, et al. The challenge in diagnosis of congenital disorders of glycosylation versus mitochondrial disorders: case report. In: Buletin de perinatologie. 2021, nr. 1(90), pp. 92-98. ISSN 1810-5289.; http://repository.usmf.md/./handle/20.500.12710/18217
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7Academic Journal
المؤلفون: Coliban, Iulia, Revenco, Ninel, Țurcan, Doina, Egorov, Vladimir, Ușurelu, Natalia, Sacară, Victoria
مصطلحات موضوعية: genetică moleculară, simptome, diagnostic, screening, tratament
وصف الملف: application/pdf
Relation: Buletin de perinatologie; COLIBAN, Iulia, REVENCO, Ninel, ȚURCAN, Doina, et al. Spinal muscular atrophy: news and perspectives. In: Buletin de perinatologie. 2020, nr. 1(86), pp. 38-42. ISSN 1810-5289.; https://www.mama-copilul.md/images/buletin-perinatologic/BP_2020/BP%201%20(2020).pdf; http://repository.usmf.md/handle/20.500.12710/17038
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8Academic Journal
المؤلفون: Țurcan, Doina, Blăniță, Daniela, Ușurelu, Natalia, Sacară, Victoria
مصطلحات موضوعية: ADN mitocondrial, mutații punctiforme, ARMS-qPCR, heteroplasmie
وصف الملف: application/pdf
Relation: Buletin de perinatologie; ȚURCAN, Doina, BLĂNIȚĂ, Daniela, UȘURELU, Natalia, SACARĂ, Victoria. Methodological approaches in the molecular genetic analysis of mitochondrial DNA in patients with common clinical features of mitochondrial disease. In: Buletin de perinatologie. 2020, nr. 1(86), pp. 28-32. ISSN 1810-5289.; https://www.mama-copilul.md/images/buletin-perinatologic/BP_2020/BP%201%20(2020).pdf; http://repository.usmf.md/handle/20.500.12710/16951
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9
المؤلفون: Țurcan, Doina, Ușurelu, Natalia, Blăniță, Daniela, Sacară, Victoria
مصطلحات موضوعية: Leigh syndrome, mitochondrial DNA mutation, mitochondrial disease
وصف الملف: application/pdf
Relation: Conferinţa ştiinţifică anuală "Cercetarea în biomedicină și sănătate: calitate, excelență și performanță", 20-22 octombrie 2021; ȚURCAN, Doina, UȘURELU, Natalia, BLĂNIȚĂ, Daniela, SACARĂ, Victoria. Leigh syndrome: a rare case report = Sindromul Leigh: caz clinic rar. In: Conferinţa ştiinţifică anuală "Cercetarea în biomedicină și sănătate: calitate, excelență și performanță", 20-22 octombrie 2021: abstract book. Chișinău: [s. n.], 2021, p. 422. ISBN 978-9975-82-223-7.; https://conferinta.usmf.md/wp-content/uploads/ABSTRACT-BOOK-Culegere-de-rezumate_21_10.pdf; http://repository.usmf.md/./handle/20.500.12710/18754
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10
المؤلفون: Țurcan, Doina, Ușurelu, Natalia, Blăniță, Daniela, Sacară, Victoria
مصطلحات موضوعية: Leigh syndrome, mitochondrial DNA mutation, mitochondrial disease
وصف الملف: application/pdf
Relation: Conferinţa ştiinţifică anuală "Cercetarea în biomedicină și sănătate: calitate, excelență și performanță", 20-22 octombrie 2021; ȚURCAN, Doina, UȘURELU, Natalia, BLĂNIȚĂ, Daniela, SACARĂ, Victoria. Leigh syndrome: a rare case report: [poster]. In: Conferinţa ştiinţifică anuală "Cercetarea în biomedicină și sănătate: calitate, excelență și performanță", 20-22 octombrie 2021: culegere de postere. 2021, p. 183.; http://repository.usmf.md/./handle/20.500.12710/19193