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- BookFarhood Saremi, editor.Summary: This book is a state-of-the art reference that presents computed tomography (CT) and magnetic resonance (MR) cardiac imaging for the diagnosis and treatment planning of adult congenital heart disease (ACHD). It highlights the advantages of CT and MR in the management of ACHD, focusing on the complementary collaboration between these two modalities where possible. CT and MR aids in the evaluation of cardiac anatomy and function, leading to the demonstration of the full spectrum of abnormalities in complex cardiac malformations and the discovery of anomalous pathologies missed by other imaging techniques.
Contents:
1. Classification and Epidemiology
2. Embryology
3. Cardiac MRI Examination: An Overview
4. Magnetic Resonance Angiography
5. Principles of CT Imaging
Echocardiographic Imaging in Adult Congenital Heart Disease
6. Echocardiographic Imaging in Adult Congenital Heart Disease
7. Right Ventricle Outflow Tract
8. Left Ventricular Outflow Tract
9. Repaired Tetralogy of Fallot
10. Transposition of the Great Arteries
11. Univentricular Heart
12. Visceroatrial Situs in Congenital Heart Disease
13. Cardiac Shunts: ASD, VSD, PDA
14. Atrioventricular Septal Defects
15. Ebstein Anomaly
16. Hypertrophic Cardiomyopathy
17. The Right Myocardium
18. CT in Pediatric Congenital Heart Disease
19. Surgical Considerations in Adult Patients with Congenital Heart Disease
20. MRI in Repaired Congenital Heart Disease
21. Cardiac CT and MR Evaluation of the Adult Fontan Patient
22. Transcatheter Interventions in Adult Congenital Heart Disease
23. Virtual Surgery in Congenital Heart Disease
24. Aortic Arch Anomalies
25. Pulmonary Hypertension in Congenital Heart Disease
26. Congenital Thoracic Venous Anomalies
27. Coronary Artery Anomalies
28. Coronary Veins
29. Congenital Pericardial Anomalies
30. Extracardiac Complications
31. Cardiac MR in Patients with Implantable Arrhythmia Devices. - ArticleBakke JL, Lawrence NL, Robinson SA, Bennett J, Bowers C.Neuroendocrinology. 1978;25(5):291-302.Neonatal rats were injected with L-dopa, 5-hydroxytryptophan (5-HTP) or 6-hydroxy-dopa (6-OH-dopa) and allowed to mature. Eye opening, vaginal opening, endocrine organ weights and pituitary hormone concentration in the serum were measured. Treatment with either the dopamine (DA) precursor or the serotonin (5-HT) precursor caused an acceleration in eye opening, a significant decrease in serum TSH (males) an elevation of serum prolactin (Prl; males), and a lowering of serum growth hormone (females). After chemical sympathectomy (6-OH-dopa) vaginal opening was delayed, thyroid weights were increased and serum TSH decreased (males). It is concluded that during the critical neonatal period overloading either of 2 of the principal monaminergic systems results in similar and persistent alterations in pituitary function. Chemical sympathectomy produced a different pattern of abnormalities.