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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Bardet-Biedl Syndrome-Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype-Phenotype Correlations von Florea, Laura, Caba, Lavinia, Gorduza, Eusebiu Vlad

Volltext

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 revie... von Gug, Cristina, Caba, Lavinia, Mozos, Ioana, Stoian, Dana, Atasie, Diter, Gug, Miruna, Gorduza, Eusebiu Vlad

Volltext

Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling von Panzaru, Monica-Cristina, Florea, Andreea, Caba, Lavinia, Gorduza, Eusebiu Vlad

Volltext

Heterogeneity in combined immunodeficiencies with associated or syndromic features (Review) von Caba, Lavinia, Gug, Cristina, Gorduza, Eusebiu Vlad

Volltext