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Lavinia Caba

Showing results (11-20 of 34) with videos related to

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Diagnostics (Basel, Switzerland)|January 8, 2023
<i>SHOX</i> Deletion and Idiopathic Short Stature: What Does the Clinician Need to Know? Case Series ReportMaria-Christina Ungureanu, Anamaria Hrisca, Lavinia Caba, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|April 20, 2011
[Chromosomal evaluation in couples with reproductive disorders--retrospective study of a selected group of 266 couples]Lăcrămioara Butnariu, M Covic, M Onofriescu, et al.
Gene|March 14, 2020
Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and review of the literatureCristina Gug, Lavinia Caba, Ioana Mozos, et al.
Metabolites|December 27, 2024
Cathelicidin: Insights into Its Impact on Metabolic Syndrome and Chronic InflammationAlina Delia Popa, Andreea Gherasim, Lavinia Caba, et al.
Metabolites|January 26, 2024
From the Sun to the Cell: Examining Obesity through the Lens of Vitamin D and InflammationAlina Delia Popa, Otilia Niță, Lavinia Caba, et al.
Cardiology Research|October 23, 2018
Holt-Oram Syndrome With Multiple Cardiac AbnormalitiesMarilena Renata Spiridon, Antoniu Octavian Petris, Eusebiu Vlad Gorduza, et al.
Nutrients|July 11, 2023
A Scoping Review of the Relationship between Intermittent Fasting and the Human Gut Microbiota: Current Knowledge and Future DirectionsAlina Delia Popa, Otilia Niță, Andreea Gherasim, et al.
Biomedicines|August 26, 2023
Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way StreetIoana Balinisteanu, Monica-Cristina Panzaru, Lavinia Caba, et al.
Life (Basel, Switzerland)|December 23, 2023
Hydatidiform Mole-Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative ReviewAndreea Florea, Lavinia Caba, Ana-Maria Grigore, et al.
Medicina (Kaunas, Lithuania)|August 6, 2021
Gorham-Stout Disease with Multiple Bone Involvement-Challenging Diagnosis of a Rare Disease and Literature ReviewAlina Momanu, Lavinia Caba, Nicoleta Carmen Gorduza, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Diagnostics (Basel, Switzerland)|January 8, 2023
<i>SHOX</i> Deletion and Idiopathic Short Stature: What Does the Clinician Need to Know? Case Series ReportMaria-Christina Ungureanu, Anamaria Hrisca, Lavinia Caba, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|April 20, 2011
[Chromosomal evaluation in couples with reproductive disorders--retrospective study of a selected group of 266 couples]Lăcrămioara Butnariu, M Covic, M Onofriescu, et al.
Gene|March 14, 2020
Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and review of the literatureCristina Gug, Lavinia Caba, Ioana Mozos, et al.
Metabolites|December 27, 2024
Cathelicidin: Insights into Its Impact on Metabolic Syndrome and Chronic InflammationAlina Delia Popa, Andreea Gherasim, Lavinia Caba, et al.
Metabolites|January 26, 2024
From the Sun to the Cell: Examining Obesity through the Lens of Vitamin D and InflammationAlina Delia Popa, Otilia Niță, Lavinia Caba, et al.
Cardiology Research|October 23, 2018
Holt-Oram Syndrome With Multiple Cardiac AbnormalitiesMarilena Renata Spiridon, Antoniu Octavian Petris, Eusebiu Vlad Gorduza, et al.
Nutrients|July 11, 2023
A Scoping Review of the Relationship between Intermittent Fasting and the Human Gut Microbiota: Current Knowledge and Future DirectionsAlina Delia Popa, Otilia Niță, Andreea Gherasim, et al.
Biomedicines|August 26, 2023
Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way StreetIoana Balinisteanu, Monica-Cristina Panzaru, Lavinia Caba, et al.
Life (Basel, Switzerland)|December 23, 2023
Hydatidiform Mole-Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative ReviewAndreea Florea, Lavinia Caba, Ana-Maria Grigore, et al.
Medicina (Kaunas, Lithuania)|August 6, 2021
Gorham-Stout Disease with Multiple Bone Involvement-Challenging Diagnosis of a Rare Disease and Literature ReviewAlina Momanu, Lavinia Caba, Nicoleta Carmen Gorduza, et al.
Pageof 4