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17 results on '"HONG‑YU SHI"'

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1. SOX17 loss-of-function variation underlying familial congenital heart disease

2. GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve

3. Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

4. KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy

5. TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome

6. TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

7. ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

8. MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

9. CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

10. Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block

11. Administration of intracoronary bone marrow mononuclear cells on chronic myocardial infarction improves diastolic function

13. Correlation between the capsaicin test and objective skin measurements in evaluating sensitive skin in Chinese females

14. Changes of dendritic cells and fractalkine in type 2 diabetic patients with unstable angina pectoris: a preliminary report

16. Peripheral-blood dendritic cells in men with coronary heart disease

17. [The role of first pass and delayed contrast-enhancement magnetic resonance imaging in patients with myocardial infarction]

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