102 results on '"Jux, Christian"'
Search Results
2. Cardiomyocyte hyperplasia and immaturity but not hypertrophy are characteristic features of patients with RASopathies
3. Edoxaban for Thromboembolism Prevention in Pediatric Patients With Cardiac Disease
4. Histopathology of congestive nephropathy: a case description and literature review.
5. Natural history of pulmonary atresia with intact ventricular septum (PAIVS) and critical pulmonary stenosis (CPS) and prediction of outcome
6. The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy"
7. Long-term outcome of perimembranous VSD closure using the Nit-Occlud® Lê VSD coil system
8. Associated Anomalies and Outcome in Patients with Prenatal Diagnosis of Aortic Arch Anomalies as Aberrant Right Subclavian Artery, Right Aortic Arch and Double Aortic Arch.
9. Somatic Development in Children with Congenital Heart Defects
10. Genetic basis of hypertrophic cardiomyopathy in children
11. Dietary protein restriction throughout intrauterine and postnatal life results in potentially beneficial myocardial tissue remodeling in the adult mouse heart
12. Left Ventricular Physiology and Ventricular-Vascular Interactions in Young Patients After Heart Transplantation.
13. Creation of a functional Potts shunt by stenting the persistent arterial duct in newborns and infants with suprasystemic pulmonary hypertension of various etiologies
14. Genetic Screening Reveals Heterogeneous Clinical Phenotypes in Patients with Dilated Cardiomyopathy and Troponin T2 Variants.
15. Pulmonary artery banding in infants and young children with left ventricular dilated cardiomyopathy: A novel therapeutic strategy before heart transplantation
16. Exercise-dependent changes in ventricular–arterial coupling and aortopulmonary collateral flow in Fontan patients: a real-time CMR study.
17. Fetal Echocardiography in Predicting Postnatal Outcome in Borderline Left Ventricle.
18. Fifteen-year Single Center Experience with the “Giessen Hybrid” Approach for Hypoplastic Left Heart and Variants: Current Strategies and Outcomes
19. Stenting of Native Right Ventricular Outflow Tract Obstructions in Symptomatic Infants
20. Beneficial Effects of Residual Right Ventricular Outflow Tract Obstruction on Right Ventricular Volume and Function in Patients After Repair of Tetralogy of Fallot
21. Novel Catheter-Interventional Strategy for Intracardiac Connecting of Total Anomalous Pulmonary Venous Return in Newborns With Hypoplastic Left Heart-Syndrome Prior to Hybrid Approach
22. Arrhythmogene rechtsventrikuläre Dysplasie/Cardiomyopathie: Diagnostik im Kindesalter
23. Two Melodies in Concert: Transcatheter Double-Valve Replacement
24. Interventional Atrial Septal Defect Closure Using a Totally Bioresorbable Occluder Matrix: Development and Preclinical Evaluation of the BioSTAR Device
25. Fate of a Modified Fenestration of Atrial Septal Occluder Device after Transcatheter Closure of Atrial Septal Defects in Elderly Patients
26. Stent Implantation of the Arterial Duct in Newborns with a Truly Duct-Dependent Pulmonary Circulation: A Single-Center Experience with Emphasis on Aspects of the Interventional Technique
27. Reversible, schwere Kardiomyopathie als Folge einer langsamen, permanenten Schmalkomplextachykardie.
28. BioSTAR® bioabsorbable septal repair implant
29. Biocompatibility of septal defect closure devices
30. Retrograde use of the Cardioseal/Starflex occluder device
31. Single Nuclei Sequencing Reveals Novel Insights Into the Regulation of Cellular Signatures in Children With Dilated Cardiomyopathy.
32. Symptom-orientated oral hygiene for children after heart transplantation: Effectiveness of a standardized prophylactic program.
33. Histopathological Workup of an Amplatzer Atrial Septal Defect Occluder After Surgical Removal
34. Interrelationship Between Hemodynamics, Brain Volumes, and Outcome in Hypoplastic Left Heart Syndrome.
35. Advances in heart failure therapy in pediatric patients with dilated cardiomyopathy.
36. Fibrotic myocardial remodeling in children and adolescents after cardiac transplantation - a CMR native T1 mapping study.
37. Prenatal Mechanistic Target of Rapamycin Complex 1 (m TORC1) Inhibition by Rapamycin Treatment of Pregnant Mice Causes Intrauterine Growth Restriction and Alters Postnatal Cardiac Growth, Morphology, and Function.
38. Hypoplastic Left Heart Syndrome (HLHS).
39. Cardiovascular magnetic resonance assessment of ventricular function and myocardial scarring before and early after repair of anomalous left coronary artery from the pulmonary artery.
40. Dexamethasone impairs growth hormone (GH)-stimulated growth, by supporession of local insulin-like growth factor (IGF)-I production and expression of GH- and IGC-1 receptor in cultured rat chondrocytes
41. Intracoronary bone marrow cell application for terminal heart failure in children.
42. Large-diameter graft-stent (Advanta V12) implantation in various locations: early results.
43. Piccolo devices in premie ductus arteriosi.
44. BioSTAR Evaluation STudy (BEST): a prospective, multicenter, phase I clinical trial to evaluate the feasibility, efficacy, and safety of the BioSTAR bioabsorbable septal repair implant for the closure of atrial-level shunts.
45. Changes in expression levels of genes involved in fatty acid metabolism: upregulation of all three members of the PPAR family (α, ?, ?) and the newly described adiponectin receptor 2, but not adiponectin receptor 1 during neonatal cardiac development of the rat
46. Origin of Electrical Activation Within the Right Atrial and Left Ventricular Walls:.
47. A New Biological Matrix for Septal Occlusion.
48. Experimental ASD closure using autologous cell-seeded interventional closure devices.
49. Experimental preseeding of the STARFlex atrial septal occluder device with autologous cells.
50. Evaluation of the Effectiveness of an Interdisciplinary Preventive Oral Hygiene Program for Children with Congenital Heart Disease.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.