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40 积分 2023-11-03 加入
FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies
7个月前
已完结
Clinical and genetic characterization of Chinese pediatric cystine stone patients
1年前
已完结
Prediction of no reflow phenomenon in percutaneous coronary intervention with optical coherence tomography and analysis of risk factors
1年前
已完结
No reflow phenomenon in percutaneous coronary interventions in ST-segment elevation myocardial infarction
1年前
已完结
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