257 results on '"Palecek, Tomas"'
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2. Abstract 13730: Genotype-Phenotype Correlates in Recent-Onset Dilated Cardiomyopathy and Their Prognostic Implications
3. Long‐term outcomes and reverse remodelling in recently diagnosed unexplained left ventricular systolic dysfunction.
4. Patisiran Treatment in Patients with Transthyretin Cardiac Amyloidosis
5. Tailored immunosuppression in biopsy‐proven immune‐mediated myocarditis.
6. Clinical indications and time schedule for cardiac magnetic resonance imaging: A joint expert opinion of the Czech Society of Cardiology and Czech Radiological Society of the Czech Medical Society J.E. Purkyne
7. The use of echocardiography in acute cardiovascular care. Summary of the document prepared by the Czech Society of Cardiology
8. IDH Mutation Analysis in Glioma Patients by CADMA Compared with SNaPshot Assay and two Immunohistochemical Methods
9. Exploratory Analyses From Apollo-B, A Phase 3 Study Of Patisiran In Patients With Attr Amyloidosis With Cardiomyopathy
10. Echocardiography and cardiac resynchronization therapy
11. Role of magnetic resonance in the detection of cardiac involvement in patients with newly diagnosed extracardiac sarcoidosis: Single center experience
12. Importance of endomyocardial biopsy in distinguishing between cardiac sarcoidosis and giant cell myocarditis: Need to distinguish between sarcoidosis and giant cell myocarditis
13. Czech Inflammatory Cardiomyopathy Immunosuppression Trial (CZECH-ICIT): Randomized, multicentric study comparing the effect of two regimens of combined immunosuppressive therapy in the treatment of inflammatory cardiomyopathy: The aims and design of the trial
14. Needle fragment embolism into the right ventricle: a rare cause of chest pain case report and literature review
15. A high frequency of viral agents yet absence of Borrelia burgdorferi is seen within the myocardium of subjects with normal left ventricular systolic function: an electron microscopy study
16. Recent-onset dilated cardiomyopathy associated with Borrelia burgdorferi infection
17. Cardiac amyloidosis: A comprehensive review
18. Mechanical heart valve prosthesis in pregnancy – multicenter retrospective observational study
19. Cardiac sarcoidosis: from diagnosis to treatment
20. Prevalence of Fabry disease in male patients with unexplained left ventricular hypertrophy in primary cardiology practice: prospective Fabry cardiomyopathy screening study (FACSS)
21. Mosaic tissue distribution of the tandem duplication of LAMP2 exons 4 and 5 demonstrates the limits of Danon disease cellular and molecular diagnostics
22. The diagnostic performance of cardiac magnetic resonance in detection of myocardial involvement in AL amyloidosis
23. Role of magnetic resonance in the detection of cardiac involvement in patients with newly diagnosed extracardiac sarcoidosis: A single-center experience.
24. 2021 ESC/EACTS Guidelines for the management of valvular heart disease
25. Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles
26. Pulmonary arterial hypertension associated with systemic sclerosis in the Czech Republic
27. Are pulmonary artery pulsatility indexes able to differentiate chronic pulmonary thromboembolism from pulmonary arterial hypertension? An echocardiographic and catheterization study
28. Left atrial flow propagation velocity: a new approach for assessment of left atrial reservoir function
29. Onset and progression of the Anderson–Fabry disease related cardiomyopathy
30. Herpes simplex virus-induced cardiomyopathy successfully treated with acyclovir
31. Presence of Borrelia burgdorferi in endomyocardial biopsies in patients with new-onset unexplained dilated cardiomyopathy
32. Papillary fibroelastoma on pulmonary valve – Valve-sparing surgery of a cardiac tumor in a rare location
33. Combined valve replacement and aortocoronary bypass in an adult mucopolysaccharidosis type VII patient
34. Death in consequence of late failure of endoscopic third ventriculostomy
35. Comparison of early diastolic annular velocities measured at various sites of mitral annulus in detection of mild to moderate left ventricular diastolic dysfunction
36. Early diastolic mitral annular velocity and color M-mode flow propagation velocity in the evaluation of left ventricular diastolic function in patients with Fabry disease
37. Dystrophic calcification of the interventricular septum mimicking cardiac tumour and role of multimodality imaging
38. Pigmentary retinopathy can indicate the presence of pathogenic LAMP2 variants even in somatic mosaic carriers with no additional signs of Danon disease
39. ALCOHOL SEPTAL ABLATION FOR SUCCESSFUL TREATMENT OF THE LEFT VENTRICULAR OUTFLOW TRACT OBSTRUCTION IN FABRY DISEASE
40. Comparison of routine contrast‑enhanced computed tomography with late gadolinium enhancement cardiac magnetic resonance imaging in the detection of myocardial pathology
41. Cardiac Structural and Functional Changes in Competitive Amateur Cyclists
42. The Evaluation of Pulmonary Hypertension Using Right Ventricular Myocardial Isovolumic Relaxation Time
43. Right Ventricular Involvement in Fabry Disease
44. Papillary Fibroelastoma Arising from the Left Ventricular Apex Associated with Nonspecific Systemic Symptoms
45. Preload Dependence of the Time Interval between Onsets of Mitral Inflow and Early Diastolic Mitral Annular Velocity: A Study in Healthy Subjects
46. Effect of Preload Reduction by Hemodialysis on Conventional and Novel Echocardiographic Parameters of Left Ventricular Structure and Function
47. Fabry Disease: Percutaneous Transluminal Septal Myocardial Ablation Markedly Improved Symptomatic Left Ventricular Hypertrophy and Outflow Tract Obstruction in a Classically Affected Male
48. Pigmentary retinopathy can indicate the presence of pathogenic LAMP2 variants even in somatic mosaic carriers with no additional signs of Danon disease.
49. Importance of endomyocardial biopsy in distinguishing between cardiac sarcoidosis and giant cell myocarditis
50. Comparison of echocardiographic parameters in Fabry cardiomyopathy and light‐chain cardiac amyloidosis
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