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Valentina Miteva
Valentina Miteva
Medical geneticist
Verified email at mu-varna.bg
Title
Cited by
Cited by
Year
Comparison between thrombophilic gene polymorphisms among high risk patients
LA Mariya Levkova, Mari Hachmeriyan, Milena Stoyanova, Valentina Miteva
Romanian Journal of Internal Medicine 58 (1), 20-26, 2020
62020
Standard karyotyping - a look through the European guidelines
LA Mari Hachmeriyan, Maria Levkova, Milena Stoyanova, Valentina Miteva
Varna Medical Forum 8 (1), 90 - 96, 2019
42019
Women’s awareness towards prenatal down syndrome tests in Bulgaria
AL Levkova Mariya, Hachmeriyan Mari, Miteva Valentina, Stoyanova Milena ...
Journal of Down Syndrome & Chromosome Abnormalities 4 (129), 1-4, 2018
2*2018
Предизвикателства на медико-генетичната консултация в ерата на геномната медицина
АЛ Хачмериян М.,Левкова М.,Стоянова М.
Обща медицина 21 (6), 37-40, 2019
12019
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
Cytogenetic analysis of patients with hematological malignancies
D Yahya, V Miteva, I Micheva, T Ruseva, L Angelova
Cytology and Genetics 57 (3), 272-281, 2023
2023
Cytogenetic findings in 126 patients with multiple myeloma A retrospective single-centre study
V Miteva, C Ruseva, Т Chervenkov, I Micheva
Archives of Hellenic medicine 40 (3), 349-355, 2023
2023
Prenatal screening – Evolution of pregnant women’s choice
AL Yahya D., Hachmeriyan M., Stoyanova M., Miteva V., Levkova M
Prenatal Diagnosis 43 (Suppl 1), 93, 2023
2023
Telegenetics: attidutes of genetic counselors and patients in Bulgaria
LA Mariya Levkova, Mari Hachmeriyan, Milena Stoyanova, Valentina Miteva
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPP 1), 570-570, 2022
2022
COVID-19 effect on post-test genetic counselling
LA Mari Hachmeriyan, Maria Levkova, Dinnar Yahya, Milena Stoyanova ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 561-561, 2022
2022
Incidental findings in cytogenetics - the old new
LA Valentina Miteva, Tsanka Ruseva, Dinnar Yahya, Marya Levkova, Milena ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 560-561, 2022
2022
Evaluation of the diagnostic rate in children with dysmorphic features-one genetic center experience
LA Milena Stoyanova, Mari Hachmeriyan, Mariya Levkova, Valentina Miteva
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 338-338, 2022
2022
Chromosomal abnormalities and their prognostic significance in patients with multiple myeloma.
V Miteva, C Ruseva, T Chervenkov, I Micheva
2022
ХРОМОЗОМНИ НАРУШЕНИЯ И ТЯХНОТО ПРЕДИКТИВНО ЗНАЧЕНИЕ ПРИ ПАЦИЕНТИ С МНОЖЕСТВЕН МИЕЛОМ.
В Митева, Ц Русева, Т Червенков, И Мичева
Medical Review/Meditsinski Pregled 58 (1), 2022
2022
ЦИТОГЕНЕТИЧНИ АБЕРАЦИИ ПРИ ПАЦИЕНТИ С МНОЖЕСТВЕН МИЕЛОМ
В Митева, М Хачмериян, Т Червенков, И Мичева
Medical Review/Meditsinski Pregled 57 (5), 2021
2021
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, ...
13th EUROPEAN CYTOGENOMICS CONFERENCE 48 (73), 2021
2021
Cytogenetic aberrations in patients with multiple myeloma.
V Miteva, M Hachmeriyan, T Chervenkov, I Micheva
2021
Цитогенетични изследвания при деца - опитът на Лаборатория по медицинска генетика - Варна за период от 10 години
ЛА М. Стоянова, М. Цветкова, М. Левкова, В. Митева, Д. Яхя, В. Йотова, М ...
Педиатрия 61 (2), 31-34, 2021
2021
A retrospective study of patients with Multiple Myeloma tested in Laboratory of Medical genetics, Varna, Bulgaria
LA V. Miteva, T. Ruseva, M. Hachmeriyan, M. Levkova
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 940-941, 2020
2020
Single - gene pathology in pediatric patients referred for genetic counseling for a period of five years
VM Milena Stoyanova, Lyudmila Angelova, Mary Hachmeriyan, Mariya Levkova
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 782-782, 2020
2020
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