| Association between polymorphic markers human leucocyte antigen-G and tumour necrosis factor alpha and susceptibility to recurrent miscarriages among Bulgarian women M Levkova, T Chervenkov, M Hachmeriyan, L Angelova Turkish Journal of Obstetrics and Gynecology 17 (1), 34, 2020 | 6 | 2020 |
| Comparison between thrombophilic gene polymorphisms among high risk patients M Levkova, M Hachmeriyan, M Stoyanova, V Miteva, L Angelova Romanian Journal of Internal Medicine 58 (1), 20-26, 2020 | 6 | 2020 |
| Maternal biochemical screening--an approach for genetic prevention. part 2. sequential approach with integrated risk assessment L Angelova, V Gadancheva, D Konstantinova, M Stoianova, ... Akusherstvo i Ginekologiia 52 (5), 14-18, 2013 | 6 | 2013 |
| CFTR gene variants as a reason for impaired spermatogenesis: a pilot study and a Meta-analysis of published data M Levkova, T Chervenkov, M Hachmeriyan, L Angelova Human Fertility 25 (4), 728-737, 2022 | 4 | 2022 |
| Double aneuploidy 48, ÕÕÕ,+ 21 of a Bulgarian newborn with Down phenotype: a case report M Tsvetkova, M Levkova, S Tsvetkova, M Hachmeriyan, E Kovachev, ... Egyptian Journal of Medical Human Genetics 21, 1-5, 2020 | 4 | 2020 |
| Standard karyotyping-a look through the European guidelines M Hachmeriyan, M Levkova, M Stoyanova, V Miteva, L Angelova Varna Medical Forum 8 (1), 90-96, 2019 | 4 | 2019 |
| Treatment with recombinant growth hormone in children with Turner syndrome: a study from a tertiary university center K Rankova, V Iotova, V Mladenov, T Karamfilova, Y Bazdarska, ... Scripta Scientifica Medica 53 (1), 9-14, 2021 | 3 | 2021 |
| Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour M Stoyanova, M Hachmeriyan, M Levkova, S Bichev, M Georgieva, ... Folia Medica 64 (1), 27-32, 2022 | 2 | 2022 |
| Challenging Reproductive Genetic Counseling in Families at High Risk for Rare Genetic Syndromes–A Case Report with Possible Denys-Drash Syndrome M Hachmeriyan, S Andonova, M Levkova, M Stoyanova, K Kalchev J Genet Disor Genet Rep 7 1, 2, 2018 | 2 | 2018 |
| Women’s awareness towards prenatal down syndrome tests in Bulgaria M Levkova, M Hachmeriyan, V Miteva, M Stoyanova, M Tsvetkova J Down Syndr Chr Abnorm 4 (129), 2472-1115.1000129, 2018 | 2 | 2018 |
| Clinical and genetic challenges in a family with history of childhood polyp, aortopathy, and clinical diagnosis of hereditary hemorrhagic teleangiectasia (HHT) LA Tanya Kadiyska, Alexander Nossikoff, Pencho Kratunkov, Mari Hachmeriyan Ann Pediatr Cardiol 9 (2), 176–178, 2016 | 2 | 2016 |
| Combination of Cri du Chat and partial trisomy 13 syndrome due to paternal balanced three way translocation- case report M Hachmeriyan, M Zeleva, M Tzvetkova, H Duba, M Maurer, J V., ... 10th Balkan congress of human genetics Bled, Slovenia 10-12 October 2013, 2013 | 2 | 2013 |
| Clinical approach to hereditary hemorragic telangiectasia M Hachmeriyan, N Sapundzhiev, M Georgieva, N Dobrudjanska, ... Journal of IMAB 19 (issue 2), 453-456, 2013 | 2 | 2013 |
| Acute myelogenous leukemia–current recommendations and approaches in molecular-genetic assessment D Yahya, M Hachmeriyan, I Micheva, T Chervenkov Romanian Journal of Internal Medicine 60 (2), 103-114, 2022 | 1 | 2022 |
| 16p11. 2 Duplication Syndrome-a Case Report M Levkova, M Stoyanova, R Staneva, M Hachmeriyan, L Angelova Folia Medica 63 (1), 138-141, 2021 | 1 | 2021 |
| Hereditary breast and ovarian cancer-genetic counseling experience report D Yahya, M Hachmeriyan, M Stoyanova, V Miteva, M Levkova, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 339-339, 2024 | | 2024 |
| MLPA in the initial genetic screening of patients with acute myeloid leukemia D Yahya, M Hachmeriyan, T Ruseva, T Chervenkov, I Micheva Romanian Journal of Internal Medicine, 2023 | | 2023 |
| A girl with ROHHAD syndrome-a rare cause of rapid-onset obesity and hypothalamic dysfunction S Galcheva, M Hachmeriyan, D Krumova, R Georgiev, Z Dancheva, ... HORMONE RESEARCH IN PAEDIATRICS 96, 255-255, 2023 | | 2023 |
| ACAN gene mutation in a patient born small for gestational age with familial short stature V Iotova, Y Deyanova, M Stoyanova, M Hachmeriyan HORMONE RESEARCH IN PAEDIATRICS 96, 338-338, 2023 | | 2023 |
| A Long-term Follow-up of a Late Diagnosed Patient with Temple Syndrome–a Case Report N Yordanova, V Iotova, DJG Mackay Journal of clinical research in pediatric endocrinology, 0-0, 2022 | | 2022 |
Lyudmila AngelovaMedical University of VarnaVerified email at mu-varna.bg
