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6. Impact of guideline directed medical therapy on myocardial function in adults with congenital heart disease

10. Multimodality Imaging in Ebstein Anomaly

11. COVID-19–Related Thrombotic and Bleeding Events in Adults With Congenital Heart Disease

12. Design of a multi-institutional neurocognitive discovery study in adult congenital heart disease (MINDS-ACHD)

17. Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort

22. COVID-19 in Adults With Congenital Heart Disease

23. A Computationally Efficient Approach for Estimation of Tissue Material Parameters from Clinical Imaging Data Using a Level Set Method.

24. Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome

25. Design and Harmonization Approach for the Multi-Institutional Neurocognitive Discovery Study (MINDS) of Adult Congenital Heart Disease (ACHD) Neuroimaging Ancillary Study: A Technical Note

27. Influence of Aortic Stiffness on Aortic-Root Growth Rate and Outcome in Patients With the Marfan Syndrome

28. Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome

30. The Use of Automated Atrial CMR Measures and a Novel Atrioventricular Coupling Index for Predicting Risk in Repaired Tetralogy of Fallot

31. Thromboprophylaxis in Patients With Fontan Circulation

32. Cardiac MRI-Derived Inferior Vena Cava Cross-Sectional Area Correlates with Measures of Fontan-Associated Liver Disease

33. Multimodality Imaging in Ebstein Anomaly

35. Hepatocellular Carcinoma After Fontan Operation: Multicenter Case Series

37. Patent foramen ovale in children: Unique pediatric challenges and lessons learned from adult literature

40. Cardiac MRI Predictors of Right Ventricular Dysfunction after the Da Silva Cone Operation for Ebstein's Anomaly

41. Hepatocellular carcinoma and the Fontan circulation: Clinical presentation and outcomes

49. CARDIOPULMONARY PRESENTATION OF A PATIENT WITH XXXY SYNDROME

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