| 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 … C Gug, L Caba, I Mozos, D Stoian, D Atasie, M Gug, EV Gorduza Gene 741, 144565, 2020 | 19 | 2020 |
| Study of the total serum concentration of serrum ionized magnesium in children and adolescents from Sibiu Area E Antonescu, G Bota, B Serb, D Atasie, C Dahm Tataru, M Totan, L Duica, ... Rev. Chimie 69 (12), 3389-3392, 2018 | 13 | 2018 |
| Epidermolysis Bullosa–Review S Kovacs, D Atasie Neonatology 2 (11), 2012 | 2 | 2012 |
| Unveiling the Pathological Mechanisms of Death Induced by SARS-CoV-2 Viral Pneumonia GC Oprinca, CI Mohor, A Oprinca-Muja, A Hașegan, AN Cristian, ... Microorganisms 12 (3), 459, 2024 | 1 | 2024 |
| Lack of Association Between BsmI and FokI Polymorphisms of the VDR Gene and Sporadic Colorectal Cancer in a Romanian Cohort—A Preliminary Study B Petre-Mandache, E Burada, MG Cucu, D Atasie, AL Riza, I Streață, ... Current Oncology 31 (10), 6406-6418, 2024 | | 2024 |
| Wolfram Syndrome Type I Case Report and Review—Focus on Early Diagnosis and Genetic Variants AD Jurca, LB Galea-Holhos, AA Jurca, D Atasie, CD Petchesi, E Severin, ... Medicina 60 (7), 1064, 2024 | | 2024 |
| The Importance of Molecular Testing in Neurofibromatosis Type 1: Rare Association between Two Mutational Variants in NF1 Gene and CRX Gene. Case Report and Short Literature Review A Jurca, CD Petchesi, MC Jurca, D Atasie, D Bembea, AD Jurca Preprints, 2024 | | 2024 |
| The Surprises of Molecular Testing in Neurofibromatosis Type 1: Rare Association between Two Mutational Variants A Jurca, CD Petchesi, MC Jurca, D Bembea, AD Jurca, D Atasie Pharmacophore 15 (2-2024), 70-78, 2024 | | 2024 |
| Dimethyl-sulfoxide is a Suitable Solvent for Fluorescent Microscopy Detection of Medium and Strong Heat Shock Inductors Using Transgenic Zebrafish V Preluca, BH Serb, S Marchian, D Atasie, MC Mitariu, A Sabau, C Tantar, ... REVISTA DE CHIMIE 69 (2), 337-340, 2018 | | 2018 |
| Noţiuni de genetică preclinică şi clinică cu aplicaţii practice necesare unui asistent medical generalist D Atasie Editura Universităţii" Lucian Blaga" din Sibiu, 2018 | | 2018 |
| The pericentric inversion on chromosome 9 (46, XY, inv (9)) (p11; q13); (46, XX, inv (9)) (p11; q13) it’s one of the causes of couple infertility A Diter, B Cosmina Romanian Journal of rare Diseases, 1, 2017 | | 2017 |
| Mosaic 46XX / 45, X / 47, XXX in a couple with a history of spontaneous miscarriage and 4 failed in vitro fertilization techniques A Diter, B Cosmina Romanian Journal of rare Diseases, 2, 2017 | | 2017 |
| Boli genetice de la A la Z D Atasie Editura Universităţii" Lucian Blaga" din Sibiu, 2016 | | 2016 |
| ANGELMAN Syndrome. Case report. A Diter, ME Claudia, M Mariela Romanian Journal of rare Diseases, 2, 2016 | | 2016 |
| Pericentric inversion of chromosome 9 the cause of infertility in a couple with 9 years primary infertility due to male A Diter, I Florin, M Mariela Romanian Journal of rare Diseases, 1, 2016 | | 2016 |
| Diagnosticul genetic de preimplantare A Diter Tendinte si Progrese in Medicina Sibiana 6, 8, 2016 | | 2016 |
| Cariotipul molecular( array CGH) A Diter Tendinte si Progrese in Medicina Sibiana 6, 7, 2016 | | 2016 |
| Tehnici moderne de genetica moleculara si inginerie genetica. A Diter Tendinte si Progrese in Medicina Sibiana 5, 13, 2016 | | 2016 |
| Farmacogenetica D Atasie Editura Universităţii" Lucian Blaga" din Sibiu, 2015 | | 2015 |
| The importance of genetic testing in a couple with 6 years primary infertility due to male A Diter, I Florin, M Mariela Romanian Journal of rare Diseases, 2, 2015 | | 2015 |
