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Lavinia Caba

Showing results (1-10 of 34) with videos related to

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Experimental and Therapeutic Medicine|December 28, 2020
Heterogeneity in combined immunodeficiencies with associated or syndromic features (Review)Lavinia Caba, Cristina Gug, Eusebiu Vlad Gorduza
Frontiers in Pediatrics|June 20, 2022
Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical ImportanceLaura Florea, Lavinia Caba, Eusebiu Vlad Gorduza
Genes|September 28, 2021
Bardet-Biedl Syndrome-Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype-Phenotype CorrelationsLaura Florea, Lavinia Caba, Eusebiu Vlad Gorduza
Archive of Clinical Cases|September 30, 2022
Pituitary hypoplasia and growth hormone deficiency in a patient with Coffin-Siris syndrome and severe short stature: case report and literature reviewStefana Catalina Bilha, Laura Teodoriu, Cristian Velicescu, et al.
World Journal of Clinical Cases|May 22, 2023
Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counselingMonica-Cristina Panzaru, Andreea Florea, Lavinia Caba, et al.
Biomolecules|December 24, 2021
Circular RNA-Is the Circle Perfect?Lavinia Caba, Laura Florea, Cristina Gug, et al.
Diagnostics (Basel, Switzerland)|June 24, 2022
Epidermolysis Bullosa-A Different Genetic Approach in Correlation with Genetic HeterogeneityMonica-Cristina Pânzaru, Lavinia Caba, Laura Florea, et al.
Journal of Multidisciplinary Healthcare|October 4, 2022
Monitoring and Management of Bardet-Biedl Syndrome: What the Multi-Disciplinary Team Can DoLavinia Caba, Laura Florea, Elena Emanuela Braha, et al.
Journal of Clinical Laboratory Analysis|June 27, 2020
Comparison between paramagnetic and CD71 magnetic activated cell sorting of fetal nucleated red blood cells from the maternal bloodDragos Nemescu, Daniela Constantinescu, Vlad Gorduza, et al.
International Journal of Molecular Sciences|November 27, 2025
The Landscape of Genetic Variation and Disease Risk in Romania: A Single-Center Study of Autosomal Recessive Carrier Frequencies and Molecular VariantsMiruna Gug, Nicoleta Andreescu, Lavinia Caba, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Experimental and Therapeutic Medicine|December 28, 2020
Heterogeneity in combined immunodeficiencies with associated or syndromic features (Review)Lavinia Caba, Cristina Gug, Eusebiu Vlad Gorduza
Frontiers in Pediatrics|June 20, 2022
Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical ImportanceLaura Florea, Lavinia Caba, Eusebiu Vlad Gorduza
Genes|September 28, 2021
Bardet-Biedl Syndrome-Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype-Phenotype CorrelationsLaura Florea, Lavinia Caba, Eusebiu Vlad Gorduza
Archive of Clinical Cases|September 30, 2022
Pituitary hypoplasia and growth hormone deficiency in a patient with Coffin-Siris syndrome and severe short stature: case report and literature reviewStefana Catalina Bilha, Laura Teodoriu, Cristian Velicescu, et al.
World Journal of Clinical Cases|May 22, 2023
Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counselingMonica-Cristina Panzaru, Andreea Florea, Lavinia Caba, et al.
Biomolecules|December 24, 2021
Circular RNA-Is the Circle Perfect?Lavinia Caba, Laura Florea, Cristina Gug, et al.
Diagnostics (Basel, Switzerland)|June 24, 2022
Epidermolysis Bullosa-A Different Genetic Approach in Correlation with Genetic HeterogeneityMonica-Cristina Pânzaru, Lavinia Caba, Laura Florea, et al.
Journal of Multidisciplinary Healthcare|October 4, 2022
Monitoring and Management of Bardet-Biedl Syndrome: What the Multi-Disciplinary Team Can DoLavinia Caba, Laura Florea, Elena Emanuela Braha, et al.
Journal of Clinical Laboratory Analysis|June 27, 2020
Comparison between paramagnetic and CD71 magnetic activated cell sorting of fetal nucleated red blood cells from the maternal bloodDragos Nemescu, Daniela Constantinescu, Vlad Gorduza, et al.
International Journal of Molecular Sciences|November 27, 2025
The Landscape of Genetic Variation and Disease Risk in Romania: A Single-Center Study of Autosomal Recessive Carrier Frequencies and Molecular VariantsMiruna Gug, Nicoleta Andreescu, Lavinia Caba, et al.
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