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

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype–Phenotype Correlations, and Precision Medicine

肾钙质沉着症的分子和遗传决定因素:机制、基因型-表型相关性及精准医学

Islam, Rehmat; Sun, Leming; Zhang, Lianbing; Popa, Setalia; Grădinaru, Andrei Cristian; Braha, Elena Emanuela; Grămescu, Mihaela; Babici, Ramona; Ailenei, Cristina; Butnariu, Lăcrămioara Ionela

Vitamin C: From Self-Sufficiency to Dietary Dependence in the Framework of Its Biological Functions and Medical Implications

维生素C:从自身摄取到膳食依赖——基于其生物学功能和医学意义

Grădinaru, Andrei Cristian; Popa, Setalia

Case Report: Practical approach to differentiating juvenile parkinsonism of genetic cause and drug-induced parkinsonism in adolescents: a case series and literature review

病例报告:鉴别青少年遗传性帕金森病和药物性帕金森病的实用方法:病例系列及文献综述

Grigore, Ioana; Butnariu, Lăcrămioara Ionela; Schreiner, Thomas Gabriel; Lupu, Vasile Valeriu; Lupu, Ancuta; Darie, Ludmila; Prăzaru, Cătălin; Țarcă, Elena; Popa, Setalia; Grigore, Ecaterina

Contralateral breast cancer in patients carrying mutations in the BRCA1∕2 gene

携带 BRCA1/2 基因突变的患者发生对侧乳腺癌

Anton, Sorana Caterina; Popa, Setalia; Anton, Carmen Rodica; Anton, Emil; Nicolaiciuc, Delia; Nicolaiciuc, Ovidiu Sebastian; Danciu, Mihai; Scripcariu, Şadiye Ioana; Crauciuc, Dragoş Valentin; Grigore, Mihaela

Current trends in breast cancer genetics, risk factors, and screening strategies

乳腺癌遗传学、风险因素和筛查策略的最新趋势

Anton, Sorana Caterina; Lazan, Alexandra; Grigore, Mihaela; Ilea, Ciprian; Scripcariu, Şadiye-Ioana; Popa, Setalia; Volovăț, Simona; Doroftei, Bogdan; Nicolaiciuc, Delia; Popovici, Diana; Costăchescu, Gabriel; Nicolaiciuc, Ovidiu Sebastian; Anton, Emil

The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients

分子遗传检测在MODY患者精准诊断、治疗和遗传咨询中的重要性

Butnariu, Lăcrămioara Ionela; Bizim, Delia Andreia; Oltean, Carmen; Rusu, Cristina; Pânzaru, Monica Cristina; Păduraru, Gabriela; Gimiga, Nicoleta; Ghiga, Gabriela; Moisă, Ștefana Maria; Țarcă, Elena; Starcea, Iuliana Magdalena; Popa, Setalia; Trandafir, Laura Mihaela

Identification of Genetic Variants Associated with Hereditary Thoracic Aortic Diseases (HTADs) Using Next Generation Sequencing (NGS) Technology and Genotype-Phenotype Correlations

利用新一代测序(NGS)技术和基因型-表型相关性鉴定与遗传性胸主动脉疾病(HTADs)相关的遗传变异

Butnariu, Lăcrămioara Ionela; Russu, Georgiana; Luca, Alina-Costina; Sandu, Constantin; Trandafir, Laura Mihaela; Vasiliu, Ioana; Popa, Setalia; Ghiga, Gabriela; Bălănescu, Laura; Țarcă, Elena

Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated with Early-Onset Neonatal Hypoglycemia: Genetic Heterogeneity Correlated with Phenotypic Variability

ABCC8基因突变引起的先天性高胰岛素血症与新生儿早期低血糖症相关:遗传异质性与表型变异性相关

Butnariu, Lăcrămioara Ionela; Bizim, Delia Andreia; Păduraru, Gabriela; Păduraru, Luminița; Moisă, Ștefana Maria; Popa, Setalia; Gimiga, Nicoleta; Ghiga, Gabriela; Bădescu, Minerva Codruța; Lupu, Ancuta; Vasiliu, Ioana; Trandafir, Laura Mihaela

Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome

关于与代谢综合征相关的致动脉粥样硬化性血脂异常遗传因素的最新数据和新见解

Butnariu, Lăcramioara Ionela; Gorduza, Eusebiu Vlad; Țarcă, Elena; Pânzaru, Monica-Cristina; Popa, Setalia; Stoleriu, Simona; Lupu, Vasile Valeriu; Lupu, Ancuta; Cojocaru, Elena; Trandafir, Laura Mihaela; Moisă, Ștefana Maria; Florea, Andreea; Stătescu, Laura; Bădescu, Minerva Codruța

Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies

黑色素瘤分子生物学中的基因组学和表观基因组学——生物标志物研究的先决条件

Zob, Daniela Luminita; Augustin, Iolanda; Caba, Lavinia; Panzaru, Monica-Cristina; Popa, Setalia; Popa, Alina Delia; Florea, Laura; Gorduza, Eusebiu Vlad