Absence of an increased wall thickness does not rule out cardiac amyloidosis-Reference-Cited by-同舟云学术

Absence of an increased wall thickness does not rule out cardiac amyloidosis

Published:2024-05-20 Issue:3 Volume:31 Page:244-246
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Muller Steven A.¹²³,Achten Anouk⁴,van der Meer Manon G.¹,Zwetsloot Peter-Paul¹,Sanders-van Wijk Sandra⁵,van der Harst Pim¹,van Tintelen J. Peter³⁶,te Riele Anneline S. J. M.¹²³,van Empel Vanessa⁴,Knackstedt Christian⁴,Oerlemans Marish I. F. J.¹³

Affiliation:

1. Department of Cardiology, University Medical Center Utrecht, Utrecht, Netherlands

2. Netherlands Heart Institute, Utrecht, Utrecht, Netherlands

3. Member of the European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart: ERN GUARD-Heart’ (ERN GUARDHEART),

4. Department of Cardiology, Maastricht University, Cardiovascular Research Institute Maastricht (CARIM), Maastricht, The Netherlands

5. Department of Cardiology, Zuyderland Medical Centre, Heerlen, The Netherlands

6. Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands

Funder

the Netherlands Cardiovascular Research Initiative, an initiative with support of the Netherlands Heart Foundation,

by the ZonMW Off Road Grant 2021 and ERC HORIZON IMPACT

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13506129.2024.2348681

Reference8 articles.

1. Evaluation of the cardiac amyloidosis clinical pathway implementation: a real-world experience

2. Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases

3. Automatic Identification of Patients With Unexplained Left Ventricular Hypertrophy in Electronic Health Record Data to Improve Targeted Treatment and Family Screening

4. Prevalence of transthyretin amyloidosis in patients with heart failure and no left ventricular hypertrophy

5. Development and Validation of a Prediction Model and Score for Transthyretin Cardiac Amyloidosis Diagnosis

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