Следене
Mari Hachmeriyan
Mari Hachmeriyan
Потвърден имейл адрес: mu-varna.bg - Начална страница
Заглавие
Позовавания
Позовавания
Година
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
82020
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
62022
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
62020
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
62013
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
42022
Double aneuploidy 48, ХХХ,+ 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
42020
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
42019
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
32021
16p11. 2 Duplication Syndrome-a Case Report
M Levkova, M Stoyanova, R Staneva, M Hachmeriyan, L Angelova
Folia Medica 63 (1), 138-141, 2021
32021
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
22022
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
22022
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
22018
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
22018
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
22016
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
22013
Clinical approach to hereditary hemorragic telangiectasia
M Hachmeriyan, N Sapundzhiev, M Georgieva, N Dobrudjanska, ...
Journal of IMAB 19 (issue 2), 453-456, 2013
22013
Tendencies of cytogenetic analysis of patients with acute myeloid leukemia–an 11-year single-centre experience report
D Yahya, T Ruseva, M Tsvetkova, M Stoyanova, M Levkova, V Miteva, ...
2
Overview of current NGS testing for male factor infertility
M Levkova, T Chervenkov, M Hachmeriyan, L Angelova
Russian Open Medical Journal 11 (1), 101, 2022
12022
The application of the facial analysis program Face2Gene in a single genetic counseling center: a retrospective study
D Yahya, M Stoyanova, M Hachmeriyan, M Levkova
Egyptian Pediatric Association Gazette 73 (1), 1, 2025
2025
NIPT Integration as a Patient-Paid Prenatal Screening Option—Observations and Challenges from a Bulgarian Genetic Counseling Center
D Yahya, M Hachmeriyan, M Stoyanova, M Levkova
Medical Sciences 13 (1), 3, 2024
2024
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