Heterogeneity in combined immunodeficiencies with associated or syndromic features (Review)

por Caba, Lavinia, Gug, Cristina, Gorduza, Eusebiu Vlad
Publicado 2021

Bardet–Biedl Syndrome—Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype–Phenotype Correlations

por Florea, Laura, Caba, Lavinia, Gorduza, Eusebiu Vlad
Publicado 2021

Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance

por Florea, Laura, Caba, Lavinia, Gorduza, Eusebiu Vlad
Publicado 2022

Pituitary hypoplasia and growth hormone deficiency in a patient with Coffin-Siris syndrome and severe short stature: case report and literature review

por Bilha, Stefana Catalina, Teodoriu, Laura, Velicescu, Cristian, Caba, Lavinia
Publicado 2022

Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling

por Panzaru, Monica-Cristina, Florea, Andreea, Caba, Lavinia, Gorduza, Eusebiu Vlad
Publicado 2023

Circular RNA—Is the Circle Perfect?

por Caba, Lavinia, Florea, Laura, Gug, Cristina, Dimitriu, Daniela Cristina, Gorduza, Eusebiu Vlad
Publicado 2021

Comparison between paramagnetic and CD71 magnetic activated cell sorting of fetal nucleated red blood cells from the maternal blood

por Nemescu, Dragos, Constantinescu, Daniela, Gorduza, Vlad, Carauleanu, Alexandru, Caba, Lavinia, Navolan, Dan Bogdan
Publicado 2020

Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity

por Pânzaru, Monica-Cristina, Caba, Lavinia, Florea, Laura, Braha, Elena Emanuela, Gorduza, Eusebiu Vlad
Publicado 2022

Monitoring and Management of Bardet-Biedl Syndrome: What the Multi-Disciplinary Team Can Do

por Caba, Lavinia, Florea, Laura, Braha, Elena Emanuela, Lupu, Valeriu Vasile, Gorduza, Eusebiu Vlad
Publicado 2022

SHOX Deletion and Idiopathic Short Stature: What Does the Clinician Need to Know? Case Series Report

por Ungureanu, Maria-Christina, Hrisca, Anamaria, Caba, Lavinia, Teodoriu, Laura, Bilha, Stefana, Preda, Cristina, Leustean, Letitia
Publicado 2022

Holt-Oram Syndrome With Multiple Cardiac Abnormalities

por Spiridon, Marilena Renata, Petris, Antoniu Octavian, Gorduza, Eusebiu Vlad, Petras, Anca Sabina, Popescu, Roxana, Caba, Lavinia
Publicado 2018

A Scoping Review of the Relationship between Intermittent Fasting and the Human Gut Microbiota: Current Knowledge and Future Directions

por Popa, Alina Delia, Niță, Otilia, Gherasim, Andreea, Enache, Armand Iustinian, Caba, Lavinia, Mihalache, Laura, Arhire, Lidia Iuliana
Publicado 2023

Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street

por Balinisteanu, Ioana, Panzaru, Monica-Cristina, Caba, Lavinia, Ungureanu, Maria-Christina, Florea, Andreea, Grigore, Ana Maria, Gorduza, Eusebiu Vlad
Publicado 2023

Gorham-Stout Disease with Multiple Bone Involvement—Challenging Diagnosis of a Rare Disease and Literature Review

por Momanu, Alina, Caba, Lavinia, Gorduza, Nicoleta Carmen, Arhire, Oana Elena, Popa, Alina Delia, Ianole, Victor, Gorduza, Eusebiu Vlad
Publicado 2021

Genomics and Epigenomics in the Molecular Biology of Melanoma—A Prerequisite for Biomarkers Studies

por Zob, Daniela Luminita, Augustin, Iolanda, Caba, Lavinia, Panzaru, Monica-Cristina, Popa, Setalia, Popa, Alina Delia, Florea, Laura, Gorduza, Eusebiu Vlad
Publicado 2022

Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome

por 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
Publicado 2023

Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population

por 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
Publicado 2022

Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review

por Resmerita, Irina, Cozma, Romica Sebastian, Popescu, Roxana, Radulescu, Luminita Mihaela, Panzaru, Monica Cristina, Butnariu, Lacramioara Ionela, Caba, Lavinia, Ilie, Ovidiu-Dumitru, Gavril, Eva-Cristiana, Gorduza, Eusebiu Vlad, Rusu, Cristina
Publicado 2020

Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome

por 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
Publicado 2021

A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature

por Popescu, Roxana, Grămescu, Mihaela, Caba, Lavinia, Pânzaru, Monica-Cristina, Butnariu, Lăcrămioara, Braha, Elena, Popa, Setalia, Rusu, Cristina, Cardos, Georgeta, Zeleniuc, Monica, Martiniuc, Violeta, Gug, Cristina, Păduraru, Luminiţa, Stamatin, Maria, Diaconu, Carmen C., Gorduza, Eusebiu Vlad
Publicado 2021