21 results on '"Devanagondi, Rajiv"'
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2. Practices and Outcomes from a Prospective, Multicenter Registry for Preterm Newborns with Pulmonary Hypertension
3. Physiological fetal vascular shunts and failure to regress: what the radiologist needs to know
4. Practices and Outcomes from a Prospective, Multicenter Registry for Preterm Newborns with Pulmonary Hypertension
5. New-Onset Anasarca in a Previously Healthy 10-year-old
6. Hemodynamic and Hematologic Effects of Histotripsy of Free-Flowing Blood: Implications for Ultrasound-Mediated Thrombolysis
7. Transcatheter Fontan Fenestration Closure: Sustained Improvements in Oxygen Saturation with Minimal Morbidity and Mortality
8. Long-Term Outcomes of Balloon Valvuloplasty for Isolated Pulmonary Valve Stenosis
9. Transient heart block following patent foramen ovale and atrial septal defect closure with Gore cardioform devices
10. The incidence of recurrent laryngeal nerve injury resulting in vocal cord paralysis following interventional congenital catheterisation procedures
11. Transcatheter occlusion of large pulmonary arteriovenous malformations using multiple devices in a neonate
12. A Tale of Two Brothers: Anomalous Coronary Arteries in Two Siblings
13. Penetrance of Mutations in Plakophilin-2 Among Families With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
14. Long‐term outcomes up to 25 years following balloon pulmonary valvuloplasty: A multicenter study
15. Long-Term Outcomes of Balloon Valvuloplasty for Isolated Pulmonary Valve Stenosis
16. Protein Losing Enteropathy After Cardiac Transplantation Successfully Treated by Stent Implantation
17. Results of coil closure of patent ductus arteriosus using a tapered tip catheter for enhanced control
18. Transcatheter occlusion of large pulmonary arteriovenous malformations using multiple devices in a neonate
19. Protein Losing Enteropathy After Cardiac Transplantation Successfully Treated by Stent Implantation
20. Neuroanatomical substrates for paroxysmal dyskinesia in lethargic mice
21. P3-41: Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia
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