939 results on '"van den Berg, Maarten P."'
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2. International shipping in a world below 2 °C
3. Spread in climate policy scenarios unravelled
4. A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients
5. Deep neural network-based clustering of deformation curves reveals novel disease features in PLN pathogenic variant carriers
6. ECG-only explainable deep learning algorithm predicts the risk for malignant ventricular arrhythmia in phospholamban cardiomyopathy
7. SCN5A-1795insD founder variant: a unique Dutch experience spanning 7 decades
8. Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathy
9. Molecular mechanisms and treatment responses of pulmonary fibrosis in severe COVID-19
10. Value of genetic testing in the diagnosis and risk stratification of arrhythmogenic right ventricular cardiomyopathy
11. Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy
12. Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy
13. Sex-specific aspects of phospholamban cardiomyopathy: The importance and prognostic value of low-voltage electrocardiograms
14. TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility
15. Introduction to Hereditary Cardiomyopathies
16. Abstract 12547: Obesity as Risk Factor for Malignant Ventricular Arrhythmias in Phospholamban Cardiomyopathy
17. Abstract 11933: Cardiac and Fibrosis-Related Biomarker Levels Do Not Predict Disease Development in Presymptomatic Phospholamban Cardiomyopathy
18. Multicentre experience with valve-sparing aortic root replacement by means of combined remodelling and external aortic ring annuloplasty in patients with Marfan syndrome
19. Co-benefits of black carbon mitigation for climate and air quality
20. Dexamethasone and tocilizumab treatment considerably reduces the value of C-reactive protein and procalcitonin to detect secondary bacterial infections in COVID-19 patients
21. Genome-wide methylation patterns in Marfan syndrome
22. Non-invasive method to detect high respiratory effort and transpulmonary driving pressures in COVID-19 patients during mechanical ventilation
23. The natural progression of a fistulizing gallstone resulting in massive gastrointestinal hemorrhage and Bouveret syndrome, a rare case
24. The costs of achieving climate targets and the sources of uncertainty
25. Distinct molecular signature of phospholamban p.Arg14del arrhythmogenic cardiomyopathy
26. Electrocardiographic Features Differentiating Arrhythmogenic Right Ventricular Cardiomyopathy From an Athlete’s Heart
27. Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy
28. Frequency of and Prognostic Significance of Cardiac Involvement at Presentation in Hereditary Transthyretin-Derived Amyloidosis and the Value of N-Terminal Pro-B-Type Natriuretic Peptide
29. Toward an effective exome-based genetic testing strategy in pediatric dilated cardiomyopathy
30. Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Collaboration
31. Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy
32. Author Correction: The phospholamban p.(Arg14del) pathogenic variant leads to cardiomyopathy with heart failure and is unresponsive to standard heart failure therapy
33. A randomized controlled trial of eplerenone in asymptomatic phospholamban p.Arg14del carriers
34. Introduction Hereditary Cardiomyopathies
35. Phospholamban immunostaining is a highly sensitive and specific method for diagnosing phospholamban p.Arg14del cardiomyopathy
36. The phospholamban p.(Arg14del) pathogenic variant leads to cardiomyopathy with heart failure and is unresponsive to standard heart failure therapy
37. Advanced respiratory monitoring in COVID-19 patients: use less PEEP!
38. Environmental co-benefits and adverse side-effects of alternative power sector decarbonization strategies
39. Phenotypic and Genetic Factors Associated with Absence of Cardiomyopathy Symptoms in PLN:c.40_42delAGA Carriers.
40. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
41. Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
42. Alternative pathways to the 1.5 °C target reduce the need for negative emission technologies
43. Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant
44. Long-Term Outcome of Alcohol Septal Ablation for Obstructive Hypertrophic Cardiomyopathy in the Young and the Elderly
45. Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy
46. Increased aortic tortuosity indicates a more severe aortic phenotype in adults with Marfan syndrome
47. The Risk for Type B Aortic Dissection in Marfan Syndrome
48. KBTBD13 is a novel cardiomyopathy gene
49. Programmed Ventricular Stimulation as an Additional Primary Prevention Risk Stratification Tool in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Study
50. Longitudinal Prediction of Ventricular Arrhythmic Risk in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy
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