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

From gene to heart: the impact of a novel SGCD variant in familial dilated cardiomyopathy

从基因到心脏:一种新型SGCD变异对家族性扩张型心肌病的影响

Kalayinia, Samira; Poopak, Amirhossein; Soveizi, Mahdieh; Maleki, Majid

MiR-6721-5p as a natural regulator of Meta-VCL is upregulated in the serum of patients with coronary artery disease

miR-6721-5p 作为 Meta-VCL 的天然调节因子,在冠状动脉疾病患者的血清中表达上调。

Gholipour, Akram; Zahedmehr, Ali; Arabian, Maedeh; Shakerian, Farshad; Maleki, Majid; Oveisee, Maziar; Malakootian, Mahshid

Exploring the potential of handgrip strength as a prognostic marker in acute decompensated heart failure with reduced ejection fraction: a cross-sectional study

探讨握力作为射血分数降低的急性失代偿性心力衰竭预后指标的潜力:一项横断面研究

Kohansal, Erfan; Adimi, Sara; Baghi, Mohammadsaleh; Soheili, Amirali; Changizi, Faraz; Jamalkhani, Sepehr; Hekmat, Elnaz; Omidvar, Razieh; Taghavi, Sepideh; Mirtajaddini, Marzieh; Jahromi, Zeinab Sadat Fattah; Behnemoon, Mahsa; Maleki, Majid; Mazloomzadeh, Saeideh; Naderi, Nasim

Epicardial adipose tissue features as a biomarker and therapeutic target in coronary artery disease.

心外膜脂肪组织可作为冠状动脉疾病的生物标志物和治疗靶点

Jolfayi Amir Ghaffari, Beheshti Ahmad Tashakori, Hosseini Seyyed Mohammadjavad, Fakhrabadi Amir Akbar, Mohebbi Bahram, Malakootian Mahshid, Maleki Majid, Pouraliakbar Hamidreza, Hosseini Saeid, Arabian Maedeh

Unraveling a novel FBN1 variant in Marfan syndrome with dilated aortic root manifestation

揭示一种与主动脉根部扩张表现相关的马凡综合征的新型FBN1变异

Sabahizadeh, Amirreza; Askarinejad, Amir; AliAkbar, Saranaz Seyed; Soveizi, Mahdieh; Houshmand, Golnaz; Mortezaeian, Hojjat; Elahifar, Amin; Maleki, Majid; Kalayinia, Samira

Exploring the c.406 C > T variant in TNNI3 gene: pathogenic insights into restrictive cardiomyopathy

探索TNNI3基因中的c.406 C > T变异:限制性心肌病的致病机制

Masoumi, Tannaz; Hesami, Hamed; Maleki, Majid; Kalayinia, Samira

Exploring and explaining nurses' resilience and developing strategies for its enhancement: an explanatory sequential mixed method study

探索和解释护士的韧性并制定增强其韧性的策略:一项解释性顺序混合方法研究

Khaleghparast, Shiva; Nayeri, Nahid Dehghan; Shabani, Fidan; Noohi, Feridoun; Maleki, Majid; Tabib, Avisa; Fathollahi, Mahmood Sheikh; Panjehbashi, Mehdi

Beyond the Beat, Next-Generation Sequencing Discovery of Novel RYR2 Gene Variant in Long QT Syndrome

超越节拍:下一代测序发现长QT综合征中新的RYR2基因变异

Kalayinia, Samira; Jolfayi, Amir Ghaffari; Soheili, Amirali; Maleki, Majid; Dalili, Mohammad; Soveizi, Mahdieh; Komijani, Saba

Unlocking the Secrets of Andersen-Tawil Syndrome: The Role of Next-Generation Sequencing in a Family With Long QT Syndrome

揭开安德森-塔维尔综合征的秘密:下一代测序技术在长QT综合征家族中的作用

Namazi, Mansoor; Naderi, Niloofar; Askarinejad, Amir; Dalili, Mohammad; Maleki, Majid; Kalayinia, Samira

Copy number variations: The potential association genetic cause in severe cardiovascular diseases with unknown aetiology

拷贝数变异:不明原因严重心血管疾病的潜在遗传关联

Zeng, Yuhong; Yuan, Zhiquan; Li, Jun; Yang, Lanqing; Li, Chengying; Xiang, Ying; Wu, Long; Xia, Tingting; Zhong, Li; Li, Yafei; Wu, Na; Naderi, Niloofar; MozafaryBazargany, MohammadHossein; Maleki, Majid; Kalayinia, Samira