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

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

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

Genetic heterogeneity in corpus callosum agenesis

por Pânzaru, Monica-Cristina, Popa, Setalia, Lupu, Ancuta, Gavrilovici, Cristina, Lupu, Vasile Valeriu, Gorduza, Eusebiu Vlad
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

CHARGE syndrome associated with de novo (I1460Rfs(*)15) frameshift mutation of CHD7 gene in a patient with arteria lusoria and horseshoe kidney

por Gug, Cristina, Gorduza, Eusebiu Vlad, Lăcătuşu, Adrian, Vaida, Monica Adriana, Bîrsăşteanu, Florin, Puiu, Maria, Stoicănescu, Dorina
Publicado 2020

Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?

por Butnariu, Lăcrămioara Ionela, Florea, Laura, Badescu, Minerva Codruta, Țarcă, Elena, Costache, Irina-Iuliana, Gorduza, Eusebiu Vlad
Publicado 2022

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

Genetic Modifying Factors of Cystic Fibrosis Phenotype: A Challenge for Modern Medicine

por Butnariu, Lăcrămioara Ionela, Țarcă, Elena, Cojocaru, Elena, Rusu, Cristina, Moisă, Ștefana Maria, Leon Constantin, Maria-Magdalena, Gorduza, Eusebiu Vlad, Trandafir, Laura Mihaela
Publicado 2021

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review

por Gavril, Eva-Cristiana, Luca, Alina Costina, Curpan, Alexandrina-Stefania, Popescu, Roxana, Resmerita, Irina, Panzaru, Monica Cristina, Butnariu, Lacramioara Ionela, Gorduza, Eusebiu Vlad, Gramescu, Mihaela, Rusu, Cristina
Publicado 2021

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

The Genetic Architecture of the Etiology of Lower Extremity Peripheral Artery Disease: Current Knowledge and Future Challenges in the Era of Genomic Medicine

por Butnariu, Lăcrămioara Ionela, Gorduza, Eusebiu Vlad, Florea, Laura, Țarcă, Elena, Moisă, Ștefana Maria, Tradafir, Laura Mihaela, Cojocaru, Elena, Luca, Alina-Costina, Stătescu, Laura, Bădescu, Minerva Codruța
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

Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review

por Arghir, Aurora, Popescu, Roxana, Resmerita, Irina, Budisteanu, Magdalena, Butnariu, Lacramioara Ionela, Gorduza, Eusebiu Vlad, Gramescu, Mihaela, Panzaru, Monica Cristina, Papuc, Sorina Mihaela, Sireteanu, Adriana, Tutulan-Cunita, Andreea, Rusu, Cristina
Publicado 2021