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1. Wild-Type ATTR Amyloidosis

4. Unlocking Diversity in Cardiovascular Clinical Research: Lessons from the SCAN-MP (Screening for Cardiac Amyloidosis with Nuclear Imaging in Minority Populations) Study

12. Temporal Outcomes of Patients Diagnosed With Transthyretin Cardiac Amyloidosis

13. Impact of vutrisiran on exploratory cardiac parameters in hereditary transthyretin‐mediated amyloidosis with polyneuropathy

14. Moving towards establishing centres of excellence in cardiac amyloidosis: an International Cardio-Oncology Society statement

15. Limitations of apical sparing pattern in cardiac amyloidosis: a multicentre echocardiographic study

16. Efficacy and Safety of Acoramidis in Transthyretin Amyloid Cardiomyopathy

18. Long-term Safety And Tolerability Of Acoramidis (AG10) In Symptomatic Transthyretin Amyloid Cardiomyopathy: 4-year Update From An Ongoing, Phase 2, Open-label Extension Study

19. Primary Results From APOLLO-B Open-label Extension Study Of Patisiran In Patients With Transthyretin Cardiac Amyloidosis

21. Impact of Interventricular Interaction on Ventricular Function

22. Assessing and managing frailty in advanced heart failure: An International Society for Heart and Lung Transplantation consensus statement

24. Effect of Eplontersen on Cardiac Structure and Function in Patients With Hereditary Transthyretin Amyloidosis

26. Abstract 12080: Comprehensive Proteomics Profiling of Human Myocardium Reveals Signaling Pathways Dysregulated in Severe Forms of Hypertrophic Cardiomyopathy

28. Abstract 14418: Prevalence, Characteristics, and Factors Associated With Atrial Fibrillation and Flutter in Patients With Transthyretin Cardiac Amyloidosis

29. Abstract 14362: The Columbia Score Predicts Incident Atrial Fibrillation and Flutter in Patients With Transthyretin Cardiac Amyloidosis

31. Abstract 13273: APOLLO-B, a Study of Patisiran in Patients With Transthyretin Cardiac Amyloidosis: Primary Long-Term Results From the Open-Label Extension Period

32. Patisiran Treatment in Patients with Transthyretin Cardiac Amyloidosis

34. Clonal Hematopoiesis in Clinical and Experimental Heart Failure With Preserved Ejection Fraction

35. Heterogeneous worldwide access and pricing of Tafamidis

38. Contributors

42. Gene Silencing Therapy in Hereditary (Variant) Transthyretin Cardiac Amyloidosis: A Puzzling Case of Decreasing Pyrophosphate Uptake on Scintigraphy

45. Discriminative Accuracy of CHA2DS2VASc Score, and Development of Predictive Accuracy Model Using Machine Learning for Ischemic Stroke in Cardiac Amyloidosis

46. Prevalence and significance of extracardiac uptake on pyrophosphate imaging in the SCAN-MP study: the first 379 cases

49. In the thick of it: hereditary cardiac amyloidosis identified by 124I-AT-01 PET imaging but not cardiac MRI or SPECT 99mTc pyrophosphate scintigraphy

50. Limited English Proficiency in Older Adults Referred to the Cardiovascular Team

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