Hasil Pencarian - Lavinia Caba

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  1. 1
    Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance

    Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance oleh Laura Florea, Lavinia Caba, Eusebiu Vlad Gorduza

    Diterbitkan 2022-06-01
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  2. 2
    Observational study on dietary patterns in pregnancy

    Observational study on dietary patterns in pregnancy oleh Alina Delia POPA, Lavinia CABA, Armand ENACHE, Carmen MIHALACHE, Ileana ANTOHE

    Diterbitkan 2021-06-01
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  3. 3
    Circular RNA—Is the Circle Perfect?

    Circular RNA—Is the Circle Perfect? oleh Lavinia Caba, Laura Florea, Cristina Gug, Daniela Cristina Dimitriu, Eusebiu Vlad Gorduza

    Diterbitkan 2021-11-01
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  4. 4
    Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity

    Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity oleh Monica-Cristina Pânzaru, Lavinia Caba, Laura Florea, Elena Emanuela Braha, Eusebiu Vlad Gorduza

    Diterbitkan 2022-05-01
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  5. 5
    <i>SHOX</i> Deletion and Idiopathic Short Stature: What Does the Clinician Need to Know? Case Series Report

    <i>SHOX</i> Deletion and Idiopathic Short Stature: What Does the Clinician Need to Know? Case Series Report oleh Maria-Christina Ungureanu, Anamaria Hrisca, Lavinia Caba, Laura Teodoriu, Stefana Bilha, Cristina Preda, Letitia Leustean

    Diterbitkan 2022-12-01
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  6. 6
    From the Sun to the Cell: Examining Obesity through the Lens of Vitamin D and Inflammation

    From the Sun to the Cell: Examining Obesity through the Lens of Vitamin D and Inflammation oleh Alina Delia Popa, Otilia Niță, Lavinia Caba, Andreea Gherasim, Mariana Graur, Laura Mihalache, Lidia Iuliana Arhire

    Diterbitkan 2023-12-01
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  7. 7
    A Scoping Review of the Relationship between Intermittent Fasting and the Human Gut Microbiota: Current Knowledge and Future Directions

    A Scoping Review of the Relationship between Intermittent Fasting and the Human Gut Microbiota: Current Knowledge and Future Directions oleh Alina Delia Popa, Otilia Niță, Andreea Gherasim, Armand Iustinian Enache, Lavinia Caba, Laura Mihalache, Lidia Iuliana Arhire

    Diterbitkan 2023-04-01
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  8. 8
    Hydatidiform Mole—Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative Review

    Hydatidiform Mole—Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative Review oleh Andreea Florea, Lavinia Caba, Ana-Maria Grigore, Lucian-Mihai Antoci, Mihaela Grigore, Mihaela I. Gramescu, Eusebiu Vlad Gorduza

    Diterbitkan 2023-12-01
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  9. 9
    Gorham-Stout Disease with Multiple Bone Involvement—Challenging Diagnosis of a Rare Disease and Literature Review

    Gorham-Stout Disease with Multiple Bone Involvement—Challenging Diagnosis of a Rare Disease and Literature Review oleh Alina Momanu, Lavinia Caba, Nicoleta Carmen Gorduza, Oana Elena Arhire, Alina Delia Popa, Victor Ianole, Eusebiu Vlad Gorduza

    Diterbitkan 2021-07-01
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  10. 10
    Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street

    Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street oleh Ioana Balinisteanu, Monica-Cristina Panzaru, Lavinia Caba, Maria-Christina Ungureanu, Andreea Florea, Ana Maria Grigore, Eusebiu Vlad Gorduza

    Diterbitkan 2023-07-01
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  11. 11
    Genomics and Epigenomics in the Molecular Biology of Melanoma—A Prerequisite for Biomarkers Studies

    Genomics and Epigenomics in the Molecular Biology of Melanoma—A Prerequisite for Biomarkers Studies oleh Daniela Luminita Zob, Iolanda Augustin, Lavinia Caba, Monica-Cristina Panzaru, Setalia Popa, Alina Delia Popa, Laura Florea, Eusebiu Vlad Gorduza

    Diterbitkan 2022-12-01
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  12. 12
    Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare Disorder

    Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare Disorder oleh Ioana Balinisteanu, Lavinia Caba, Andreea Florea, Roxana Popescu, Laura Florea, Maria-Christina Ungureanu, Letitia Leustean, Eusebiu Vlad Gorduza, Cristina Preda

    Diterbitkan 2024-08-01
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  13. 13
    Clinical Aspects of a Rare Disease: Bardet Biedl Syndrome

    Clinical Aspects of a Rare Disease: Bardet Biedl Syndrome oleh Ina Ofelia FOCSA, Magdalena BUDISTEANU, Cristina STOICA, Florina NEDELEA, Claudia JURCA, Lavinia CABA, Lacramioara BUTNARIU, Monica PANZARU, Cristina RUSU, Mihaela BALGRADEAN

    Diterbitkan 2022-03-01
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  14. 14
    Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome

    Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome oleh Cristian-Gabriel Ciobanu, Irina Nucă, Roxana Popescu, Lucian-Mihai Antoci, Lavinia Caba, Anca Viorica Ivanov, Karina-Alexandra Cojocaru, Cristina Rusu, Cosmin-Teodor Mihai, Monica-Cristina Pânzaru

    Diterbitkan 2023-05-01
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  15. 15
    Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population

    Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population oleh Cristina Gug, Ioana Mozos, Adrian Ratiu, Anca Tudor, Eusebiu Vlad Gorduza, Lavinia Caba, Miruna Gug, Catalina Cojocariu, Cristian Furau, Gheorghe Furau, Monica Adriana Vaida, Dorina Stoicanescu

    Diterbitkan 2022-01-01
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  16. 16
    Novel Mutation in <i>APC</i> Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome

    Novel Mutation in <i>APC</i> Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome oleh Cristina Antohi, Danisia Haba, Lavinia Caba, Mihai Liviu Ciofu, Vasile-Liviu Drug, Oana-Bogdana Bărboi, Bogdan Ionuț Dobrovăț, Monica-Cristina Pânzaru, Nicoleta Carmen Gorduza, Vasile Valeriu Lupu, Doina Dimofte, Cristina Gug, Eusebiu Vlad Gorduza

    Diterbitkan 2021-08-01
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