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Hereditary Transthyretin Amyloidosis: How to Differentiate Carriers and Patients Using Speckle-Tracking Echocardiography.

• Authors : Di Lisi, Daniela^1,2 (AUTHOR) ; Brighina, Filippo³ (AUTHOR); Manno, Girolamo^1,2 (AUTHOR)

• Source: Diagnostics (2075-4418). Dec2023, Vol. 13 Issue 24, p3634. 11p.

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Opportunities for Earlier Diagnosis and Treatment of Cardiac Amyloidosis.

• Authors : MARTYN, TREJEEVE^1,2 ; CARMONA RUBIO, ANDRES^1,2; ESTEP, JERRY D.^2,3

• Source: Methodist DeBakey Cardiovascular Journal. 2022, Vol. 18 Issue 5, p27-39. 13p.

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Ventricular arrhythmia burden and implantable cardioverter‐defibrillator outcomes in transthyretin cardiac amyloidosis.

• Authors : Brown, Matthew T.¹ ; Yalamanchili, Sreeram²; Evans, Sean T.³

• Source: Pacing & Clinical Electrophysiology. Apr2022, Vol. 45 Issue 4, p443-451. 9p.

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CMR-based T1-mapping offers superior diagnostic value compared to longitudinal strain-based assessment of relative apical sparing in cardiac amyloidosis.

• Authors : Korthals, Dennis¹; Chatzantonis, Grigorios¹; Bietenbeck, Michael¹

• Source: Scientific Reports. 7/30/2021, Vol. 11 Issue 1, p1-9. 9p.

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Quantitative [18F]florbetapir PET/CT may identify lung involvement in patients with systemic AL amyloidosis.

• Authors : Khor, Yiu Ming¹ (AUTHOR); Cuddy, Sarah² (AUTHOR); Harms, Hendrik J.¹ (AUTHOR)

• Source: European Journal of Nuclear Medicine & Molecular Imaging. Jul2020, Vol. 47 Issue 8, p1998-2009. 12p. 3 Color Photographs, 3 Charts, 4 Graphs.

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Haematological response and overall survival in two consecutive Dutch patient cohorts with AL amyloidosis diagnosed between 2008 and 2016.

• Authors : Rutten, Karlijn H. G.¹; Raymakers, Reinier A. P.¹; Hazenberg, Bouke P. C.²

• Source: Amyloid. Dec2018, Vol. 25 Issue 4, p227-233. 7p.

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Systemic amyloidosis: A challenge to the anaesthesiologists.

• Authors : Rapeti, Kalyani¹ (AUTHOR); Kamal, Manoj¹ (AUTHOR); Paliwal, Bharat¹ (AUTHOR)

• Source: Indian Journal of Anaesthesia. Jul2020, Vol. 64 Issue 7, p640-642. 3p.

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Special Issue "Multimodality Imaging in Cardiomyopathies".

• Authors : D'Andrea, Antonello^1,2 (AUTHOR) ; Bossone, Eduardo³ (AUTHOR) ; Palermi, Stefano⁴ (AUTHOR)

• Source: Journal of Clinical Medicine. Jul2022, Vol. 11 Issue 14, p4197-4197. 2p.

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Cardiac amyloidosis and surgery: What do we know about rare diseases?

• Authors : Mestres, Carlos A.^1,2 (AUTHOR) ; Van Hemelrijck, Mathias¹ (AUTHOR)

• Source: Journal of Cardiac Surgery. Aug2021, Vol. 36 Issue 8, p2911-2912. 2p.

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Cardiac Amyloidosis Treatment.

• Authors : Stern LK; Smidt Heart Institute, Cedars-Sinai, Los Angeles, California, US.; Patel J

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/complications ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/diagnosis ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/therapy

• Source: Methodist DeBakey cardiovascular journal [Methodist Debakey Cardiovasc J] 2022 Mar 14; Vol. 18 (2), pp. 59-72. Date of Electronic Publication: 2022 Mar 14 (Print Publication: Publisher: Methodist DeBakey Heart & Vascular Center Country of Publication: United States NLM ID: 101508600 Publication Model: eCollection Cited Medium:

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