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Victoria Sacara

Observed names: Sacara, Victoria, Sacară, Victoria, V. Sacara, Victoria SACARA, Victoria Sacară
ORCID: 0000-0001-9200-0494
Observed ORCID: 0000-0001-9200-0494
OpenAlex ID: A5006584080
No clinical utility of common polymorphisms in IGF1, IRS1, GCKR, PPARG, GCK1 and KCTD1 genes previously associated with insulin resistance in overweight children from Romania and Moldova
2018 · Adela Chirita-Emandi, Diana Munteanu, et al. · Journal of Pediatric Endocrinology and Metabolism · 7
Inborn Errors of Immunity in the Republic of Moldova: Advances and Hope
2023 · Svetlana Sciuca, Cristina Tomacinschii, et al. · Journal of Clinical Immunology · 2
The screening by isoelectric focusing of transferrin for the diagnosis of congenital disorders of glycosylation
2021 · Daniela Blanita, Chiril Boiciuc, et al. · The Moldovan Medical Journal · 2
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Newborn Screening for Spinal Muscular Atrophy in the Republic of Moldova: A Feasibility Study and First Steps
2026 · Iulia Coliban, Natalia Usurelu, et al. · International Journal of Neonatal Screening · 1
Cardiomyopathy secondary to Duchenne muscular dystrophy in children
2021 · Iulia Rodoman, Ina Palii, et al. · The Moldovan Medical Journal · 1
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Analiza molecular-genetică a unor boli monogenice ale sistemului nervos în Republica Moldova
2007 · Victoria Sacara · Buletinul Academiei de Ştiinţe a Moldovei. Ştiinţe Medicale · 1
Molecular-genetic Aspects and the Importance of Newborn Screening in Primary Immunodeficiencies
2026 · Plîngău, Ecaterina, Sacară, Victoria · Arta Medica
Clinical and genetic spectrum in a cohort of patients with suspected mitochondrial disease
2026 · Doina Secu, Daniela Blanita, et al. · Folia Medica
Algorithmic approach to the diagnosis of mitochondrial disorders: integrating clinical, biochemical, and genomic data
2026 · Doina Secu, Daniela Blanita, et al. · Moldovan Journal of Health Sciences
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Diagnostic challenges in suspected mitochondrial disease: Clinical, metabolic, and genetic findings
2026 · Doina Secu, Daniela Blanita, et al. · Acta Medica
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Growth patterns in duchenne muscular dystrophy
2026 · Iulia RODOMAN, Victoria SACARA, et al. · One Health & Risk Management
Exploring the clinical spectrum of DiGeorge syndrome
2026 · Cristina Tomacinschi, Victoria Sacara, et al. · Moldovan Journal of Health Sciences
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Clinical, biochemical, and genetic distinctions in patients with mitochondrial involvement versus other genetic disorders
2025 · Doina SECU, Daniela BLANITA, et al. · One Health & Risk Management
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Clinical, biochemical, and genetic findings in a group of patients evaluated for suspected mitochondrial disorders
2025 · Doina Secu, Daniela Blanita, et al. · XIth International Congress of Geneticists and Breeders from the Republic of Moldova
From validation to application: implementing a cost-effective qPCR assay for presymptomatic and symptomatic SMA diagnosis
2025 · Iulia Coliban, Natalia Usurelu, et al. · XIth International Congress of Geneticists and Breeders from the Republic of Moldova
Congenital disorders of glycosylation - diagnosis experience in the Republic of Moldova
2025 · Daniela Blanita, Chiril Boiciuc, et al. · Moldovan Journal of Health Sciences
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WED-350 Missense mutation predominates in moldavian patients with Wilson’s disease
2025 · Veronica Cumpata, Adela Turcanu, et al. · Journal of Hepatology
SAT-399-YI Detection of rare mutations of Wilson’s disease during family screening
2025 · Veronica Cumpata, Victoria Sacara, et al. · Journal of Hepatology
The impact of family screening in patients with Wilson’s disease from the Republic of Moldova
2024 · Veronica Cumpata, Adela Turcan, et al. · Moldovan Journal of Health Sciences
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Incidenţa trombofiliei ereditare la femeile cu complicaţii obstetricale în anamneză
2024 · Diana Mitriuc, Valentin Friptu, et al. · Obstetrica şi Ginecologia
Analysis of SMN1, NAIP and GTF2H2 gene status in correlation with spinal muscular atrophy
2023 · Iulia Coliban, Victoria Sacara · Moldovan Journal of Health Sciences
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First manifestation and evolution of early left ventricular dysfunction in children with Duchenne muscular dystrophy
2021 · Iulia Rodoman, Alexandr Dorif, et al. · The Moldovan Medical Journal
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Analysis of clinical and molecular genetic characteristics of Wiskott-Aldrich syndrome and X-linked thrombocytopenia
2021 · Doina TURCAN, Lucia ANDRIES, et al. · One Health & Risk Management
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Incidence rate of common hereditary neuromuscular diseases in the Republic of Moldova
2021 · Victoria Sacara · XIth International Congress of Geneticists and Breeders from the Republic of Moldova
Molecular-genetic diagnosis of Wilson disease in Republic of Moldova
2021 · Victoria Hlistun, Chiril Boiciuc, et al. · XIth International Congress of Geneticists and Breeders from the Republic of Moldova
Works count: 42
Citation count: 14
H-index: 2
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