| Genetic heterogeneity in corpus callosum agenesis MC Pânzaru, S Popa, A Lupu, C Gavrilovici, VV Lupu, EV Gorduza Frontiers in Genetics 13, 958570, 2022 | 10 | 2022 |
| The genetic architecture of vascular anomalies: current data and future therapeutic perspectives correlated with molecular mechanisms LI Butnariu, EV Gorduza, L Florea, E Țarcă, ȘM Moisă, LM Trandafir, ... International Journal of Molecular Sciences 23 (20), 12199, 2022 | 6 | 2022 |
| Genomics and Epigenomics in the Molecular Biology of Melanoma—A Prerequisite for Biomarkers Studies DL Zob, I Augustin, L Caba, MC Panzaru, S Popa, AD Popa, L Florea, ... International journal of molecular sciences 24 (1), 716, 2022 | 4 | 2022 |
| Epidemiological characteristics of peripheral artery disease: retrospective study S Popa, G Baroi, RF Popa, MD Datcu, V Aursulesei Rev Med Chir Soc Med Nat Iasi 117 (1), 96-99, 2013 | 3 | 2013 |
| Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome LI Butnariu, EV Gorduza, E Țarcă, MC Pânzaru, S Popa, S Stoleriu, ... Diagnostics 13 (14), 2348, 2023 | 2 | 2023 |
| 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 R Popescu, M Grămescu, L Caba, MC Pânzaru, L Butnariu, E Braha, ... Genes 12 (12), 1957, 2021 | 2 | 2021 |
| Preliminary evaluation of proprotein convertase subtilisin/kexin type 5 mutations in lower extremity artery disease SAV Popa, EV Gorduza, II Costache Biomed Res. 28 (10), 4676-4679, 2017 | 2 | 2017 |
| Genetic Heterogeneity Correlated with Phenotypic Variability in Congenital Hyperinsulinism Caused by Mutation in ABCC8 Gene Associated with Early‐Onset Persistent Neonatal … LI Butnariu, DA Bizim, G Păduraru, L Păduraru, ȘM Moisă, S Popa, ... Preprints, 2024 | | 2024 |
| OCULO-AURICULO-VERTEBRAL SPECTRUM: CLINICAL FEATURES IN A COHORT OF 37 PATIENTS I RESMERIȚĂ, BM COBZEANU, P Setalia, EC GAVRIL, V MARTINIUC, ... The Medical-Surgical Journal 125 (4), 578-584, 2021 | | 2021 |
| A NATURAL OPIOID DRUG RELEASED BY A1 BETA-CASEIN MILK PROTEIN DIGESTION WAS REPORTED TO BE RELATED TO VARIOUS PATHOLOGIES SP A.C. GRĂDINARU , I.V. PETRESCU-MAG , Mădălina Elena HENEA , Mariana GRECU ... Rev Rom Med Vet 31 (3), 85-90, 2021 | | 2021 |
| HIGH RISK PREGNANCY FOR ACHONDROPLASIA AND THE IMPORTANCE OF IgG AVIDITY TEST FOR DATING THE INFECTION WITH TOXOPLASMA GONDII. CASE REPORT R Irina, P Setalia, GO Cornelia, D Mihaela, F Ioana, M Elena The Medical-Surgical Journal 125 (1), 132-138, 2021 | | 2021 |
| Correlation between reason to apply a prenatal diagnosis for aneuploidy and the results of test-A retrospective study on 2,881 foetus investigated in last 15 years by FISH … V Martiniuc, M Gramescu, S Popa, R Popescu, A Paduret, I Resmerita, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1204-1204, 2019 | | 2019 |
| A rare case of chromosomal mosaicism with seven cellular lines that contains a jumping translocation that imply the chromosome 14 in a newborn with craniofacial dysmorphia and … M Gramescu, L Caba, R Popescu, S Popa, V Martiniuc, L Paduraru, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 360-361, 2019 | | 2019 |
| Genetic and Epigenetic Markers in Colorectal Cancer GEV Caba L., Drug V., Gramescu M., Panzaru M., Butnariu L.a, Popescu R ... Proceedings of 5th Medical Genetics Congress with International …, 2019 | | 2019 |
| How Important Remain the Chromosomal Analyses in Genomic Era? – Data from a Cytogenetic Study in Cohort Of 442 Individuals with Reproductive Troubles GEV Martiniuc V., Grămescu M., Popa S., Gorduza O. C Proceedings of 5th Medical Genetics Congress with International …, 2019 | | 2019 |
| Clinical and Cytogenetic Characterisation of Patients with Down Syndrome GEV Pădureț I. A., Martiniuc V., Grămescu M., Bujoran C., Graur E., Păduraru ... Proceedings of 5th Medical Genetics Congress with International …, 2019 | | 2019 |
| Congenital Heart Defects in Charge Syndrome GEV Rusu C. Pânzaru M.-C., Butnariu L.-I., Caba L., Popescu R., Popa S ... Proceedings of 5th Medical Genetics Congress with International …, 2019 | | 2019 |
| Case Report and Literature Discussion in Thrombocytopenia and Absent Radius Syndrome GEV Popa S., Mihai I., Streata I., Burada F., Bivoleanu A., Pavaloaia O. M ... Proceedings of 5th Medical Genetics Congress with International …, 2019 | | 2019 |
| A case of inherited t (4; 10)(q26; q26. 2) chromosomal translocation elucidated by multiple chromosomal and molecular analyses M Gramescu, L Caba, M Panzaru, L Butnariu, E Braha, R Popescu, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 954-954, 2018 | | 2018 |
| ArrayCGH study of Romanian patients with intellectual disability, developmental delay and malformations M Zeleniuc, P Gurban, G Dinulescu, V Plaiasu, EV Gorduza, CC Diaconu, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 924-924, 2018 | | 2018 |
Gorduza EVMedical Genetics Department, University of Medicine and Pharmacy "Grigore T. Popa" Iasi, Romaniaכתובת אימייל מאומתת בדומיין umfiasi.ro
