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

Lung Ultrasound and Ultrasound Score: A Useful Tool in Neonatal Intensive Care Units for the Diagnosis and Therapeutic Management of Newborns With Respiratory Pathology

肺部超声和超声评分：新生儿重症监护病房中用于诊断和治疗呼吸系统疾病新生儿的实用工具

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.66064
Popa, Alexandra E; Popescu, Simona D; Tecuci, Adriana; Vladareanu, Simona
呼吸系统疾病
发表日期：2024
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Current Trends in the Imaging Diagnosis of Neonatal Respiratory Distress Syndrome (NRDS): Chest X-ray Versus Lung Ultrasound

新生儿呼吸窘迫综合征（NRDS）影像诊断的最新进展：胸部X光检查与肺部超声检查的比较

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.69787
Popa, Alexandra E; Popescu, Simona D; Tecuci, Adriana; Bot, Mihaela; Vladareanu, Simona
发表日期：2024
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Unusual Presentation of Thoracic Epidural Ewing Sarcoma in a 20-Year-Old Patient: A Case Report

20岁患者胸段硬膜外尤文氏肉瘤的罕见表现：病例报告

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.62902
Markov, Daniel; Bechev, Kristian I; Markov, Galabin; Hadzhieva, Simona D; Aleksiev, Vladimir; Poryazova, Elena G
发表日期：2024
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Overlap in synaptic neurological condition susceptibility pathways and the neural pannexin 1 interactome revealed by bioinformatics analyses

生物信息学分析揭示了突触神经系统疾病易感通路与神经连接蛋白1相互作用组的重叠

期刊:Channels
影响因子:3.2
doi:10.1080/19336950.2023.2253102
Frederiksen, Simona D; Wicki-Stordeur, Leigh E; Swayne, Leigh Anne
信号转导
神经科学
发表日期：2023
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Variability in genome-engineering source materials: consider your starting point

基因组工程来源材料的变异性：考虑您的起点

期刊:Synthetic Biology
影响因子:2.5
doi:10.1093/synbio/ysad003
Patange, Simona; D Miller, Sierra; D Maragh, Samantha
发表日期：2023
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Rare disorders have many faces: in silico characterization of rare disorder spectrum

罕见病具有多种表现形式：罕见病谱的计算机模拟表征

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-022-02217-9
Frederiksen, Simona D; Avramović, Vladimir; Maroilley, Tatiana; Lehman, Anna; Arbour, Laura; Tarailo-Graovac, Maja
发表日期：2022
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Panel-based genetic testing for inherited retinal disease screening 176 genes

基于基因组的遗传性视网膜疾病筛查基因检测（176个基因）

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.1663
Sheck, Leo H N; Esposti, Simona D; Mahroo, Omar A; Arno, Gavin; Pontikos, Nikolas; Wright, Genevieve; Webster, Andrew R; Khan, Kamron N; Michaelides, Michel
发表日期：2021
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Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy

15q染色体BP3至BP5缺失可能是言语发育迟缓和语言障碍的致病基因位点：一个四口之家和一名无关男孩的病例报告

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.1109
Pavone, Piero; Ruggieri, Martino; Marino, Simona D; Corsello, Giovanni; Pappalardo, Xena; Polizzi, Agata; Parano, Enrico; Romano, Catia; Marino, Silvia; Praticò, Andrea Domenico; Falsaperla, Raffaele
发育与干细胞
发表日期：2020
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A novel GABRB3 variant in Dravet syndrome: Case report and literature review

Dravet综合征中一种新的GABRB3变异：病例报告及文献综述

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.1461
Pavone, Piero; Pappalardo, Xena Giada; Marino, Simona D; Sciuto, Laura; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Piccione, Maria; Falsaperla, Raffaele
发表日期：2020
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Perivascular neurotransmitters: Regulation of cerebral blood flow and role in primary headaches

血管周围神经递质：调节脑血流及其在原发性头痛中的作用

期刊:Journal of Cerebral Blood Flow and Metabolism
影响因子:4.5
doi:10.1177/0271678X17747188
Frederiksen, Simona D; Haanes, Kristian A; Warfvinge, Karin; Edvinsson, Lars
神经科学
发表日期：2019
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