日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetic counselors' perspectives on the expanded use of non-invasive prenatal testing

遗传咨询师对扩大无创产前检测应用范围的看法

Levkova, Mariya; Yaneva, Andreya

Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in Bulgaria

保加利亚一家中心五年来的遗传性癌症综合征遗传咨询经验

Hachmeriyan, Mari; Levkova, Mariya; Yahya, Dinnar; Stoyanova, Milena; Dimitrova, Eleonora

Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center Experience

下一代测序技术在罕见儿科遗传疾病诊断中的应用:单中心经验

Stoyanova, Milena; Yahya, Dinnar; Hachmeriyan, Mari; Levkova, Mariya

Clinical Utility of Multiplex Ligation-Dependent Probe Amplification in the Genetic Assessment of Patients with Myelodysplastic Syndrome

多重连接依赖性探针扩增技术在骨髓增生异常综合征患者基因检测中的临床应用

Valeva, Radostina; Levkova, Maria; Yahya, Dinnar; Hachmeriyan, Mari; Micheva, Ilina

Two Decades of Huntington's Disease in Varna, Bulgaria: A Retrospective Single-Centre Study of Clinical Trends and Challenges

保加利亚瓦尔纳亨廷顿病二十年回顾性单中心临床趋势与挑战研究

Levkova, Mariya; Tsalta-Mladenov, Mihael; Stoyanova, Milena; Hachmeriyan, Mari; Angelova, Lyudmila; Kaprelyan, Ara

A Novel Frameshift Variant in the SPAST Gene Causing Hereditary Spastic Paraplegia in a Bulgarian-Turkish Family

保加利亚-土耳其家族中SPAST基因的一种新型移码变异导致遗传性痉挛性截瘫

Levkova, Mariya; Tsalta-Mladenov, Mihael; Kaprelyan, Ara

Genomic Evaluation of AML-Main Techniques and Novel Approaches

急性髓系白血病基因组评估——主要技术和新方法

Yahya, Dinnar; Stoyanova, Milena; Hachmeriyan, Mari; Levkova, Mariya

Ethical and Psychosocial Issues Associated with Genetic Testing for Hereditary Tumor Predisposition Syndromes

与遗传性肿瘤易感综合征基因检测相关的伦理和社会心理问题

Hachmeriyan, Mari; Levkova, Mariya; Yahya, Dinnar; Stoyanova, Milena; Dimitrova, Eleonora

Case-control study of autonomic symptoms in the setting of Long COVID with tilt table testing

利用倾斜试验对新冠长期症状患者进行自主神经症状的病例对照研究

Durstenfeld, Matthew S; Mataraarachchi, Nirosh; Peluso, Michael J; Levkova-Clark, Marta; Schaffer, Veronica; Fehrman, Emily A; Anderson, Grace; Flores, Diana; Henrich, Timothy J; Long, Carlin S; Deeks, Steven G; Hsue, Priscilla Y

An Ultra-Rare Disorder: Case Report on Cerebrotendinous Xanthomatosis

一种极其罕见的疾病:脑腱黄瘤病病例报告

Levkova, Mariya; Hachmeriyan, Mari; Grudkova, Margarita; Tsalta-Mladenov, Mihael; Kaprelyan, Ara