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Systemic amyloidosis

The Lancet (British edition), 2016-06, Vol.387 (10038), p.2641-2654

2016

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EULAR recommendations for the management of familial Mediterranean fever

Annals of the rheumatic diseases, 2016-04, Vol.75 (4), p.644-651

2016

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Natural History, Quality of Life, and Outcome in Cardiac Transthyretin Amyloidosis

Circulation (New York, N.Y.), 2019-07, Vol.140 (1), p.16-26

2019

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New Criteria for Response to Treatment in Immunoglobulin Light Chain Amyloidosis Based on Free Light Chain Measurement and Cardiac Biomarkers: Impact on Survival Outcomes

Journal of clinical oncology, 2012-12, Vol.30 (36), p.4541-4549

2012

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Impact of Earlier Diagnosis in Cardiac ATTR Amyloidosis Over the Course of 20 Years

Circulation (New York, N.Y.), 2022-11, Vol.146 (22), p.1657-1670

2022

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Noncontrast T1 Mapping for the Diagnosis of Cardiac Amyloidosis

JACC. Cardiovascular imaging, 2013-04, Vol.6 (4), p.488-497

2013

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Prevalence of Cardiac Amyloidosis in Patients Referred for Transcatheter Aortic Valve Replacement

Journal of the American College of Cardiology, 2018-01, Vol.71 (4), p.463-464

2018

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Prognostic Value of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Cardiac Amyloidosis

Circulation (New York, N.Y.), 2015-10, Vol.132 (16), p.1570-1579

2015

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Prevalence and outcome of dual aortic stenosis and cardiac amyloid pathology in patients referred for transcatheter aortic valve implantation

European heart journal, 2020-08, Vol.41 (29), p.2759-2767

2020

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Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations

Human mutation, 2014-09, Vol.35 (9), p.E2403-E2412

2014

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CMR-Based Differentiation of AL and ATTR Cardiac Amyloidosis

JACC. Cardiovascular imaging, 2014-02, Vol.7 (2), p.133-142

2014

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Native T1 Mapping in Transthyretin Amyloidosis

JACC. Cardiovascular imaging, 2014-02, Vol.7 (2), p.157-165

2014

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Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis

European heart journal, 2017-06, Vol.38 (24), p.1905-1908

2017

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Echocardiographic phenotype and prognosis in transthyretin cardiac amyloidosis

European heart journal, 2020-04, Vol.41 (14), p.1439-1447

2020

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High Prevalence of Intracardiac Thrombi in Cardiac Amyloidosis

Journal of the American College of Cardiology, 2019-04, Vol.73 (13), p.1733-1734

2019

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Clinical Importance of Left Atrial Infiltration in Cardiac Transthyretin Amyloidosis

JACC. Cardiovascular imaging, 2022-01, Vol.15 (1), p.17-29

2022

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Pathophysiology and treatment of systemic amyloidosis

Nature reviews. Nephrology, 2013-10, Vol.9 (10), p.574-586

2013

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CMR-Verified Regression of Cardiac AL Amyloid After Chemotherapy

JACC. Cardiovascular imaging, 2018-01, Vol.11 (1), p.152-154

2018

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Characteristics and natural history of early-stage cardiac transthyretin amyloidosis

European heart journal, 2022-07, Vol.43 (27), p.2622-2632

2022

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A comparison of immunohistochemistry and mass spectrometry for determining the amyloid fibril protein from formalin-fixed biopsy tissue

Journal of clinical pathology, 2015-04, Vol.68 (4), p.314-317

2015

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Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis

PloS one, 2017-07, Vol.12 (7), p.e0181874-e0181874

2017

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Natural history and outcome of light chain deposition disease

Blood, 2015-12, Vol.126 (26), p.2805-2810

2015

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Rapid hematologic responses improve outcomes in patients with very advanced (stage IIIb) cardiac immunoglobulin light chain amyloidosis

Haematologica (Roma), 2018-04, Vol.103 (4), p.e165-e168

2018

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Limited utility of Mayo 2012 cardiac staging system for risk stratification of patients with advanced cardiac AL amyloidosis - analysis of a uniformly treated cohort of 1,275 patients

Haematologica (Roma), 2024-05, Vol.109 (5), p.1598

2024

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Systemic amyloidosis

EULAR recommendations for the management of familial Mediterranean fever

Natural History, Quality of Life, and Outcome in Cardiac Transthyretin Amyloidosis

New Criteria for Response to Treatment in Immunoglobulin Light Chain Amyloidosis Based on Free Light Chain Measurement and Cardiac Biomarkers: Impact on Survival Outcomes

Impact of Earlier Diagnosis in Cardiac ATTR Amyloidosis Over the Course of 20 Years

Noncontrast T1 Mapping for the Diagnosis of Cardiac Amyloidosis

Prevalence of Cardiac Amyloidosis in Patients Referred for Transcatheter Aortic Valve Replacement

Prognostic Value of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Cardiac Amyloidosis

Prevalence and outcome of dual aortic stenosis and cardiac amyloid pathology in patients referred for transcatheter aortic valve implantation

Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations

CMR-Based Differentiation of AL and ATTR Cardiac Amyloidosis

Native T1 Mapping in Transthyretin Amyloidosis

Multiparametric Echocardiography Scores for the Diagnosis of Cardiac Amyloidosis

Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis

Echocardiographic phenotype and prognosis in transthyretin cardiac amyloidosis

High Prevalence of Intracardiac Thrombi in Cardiac Amyloidosis

Clinical Importance of Left Atrial Infiltration in Cardiac Transthyretin Amyloidosis

Pathophysiology and treatment of systemic amyloidosis

CMR-Verified Regression of Cardiac AL Amyloid After Chemotherapy

Characteristics and natural history of early-stage cardiac transthyretin amyloidosis

A comparison of immunohistochemistry and mass spectrometry for determining the amyloid fibril protein from formalin-fixed biopsy tissue

Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis

Natural history and outcome of light chain deposition disease

Rapid hematologic responses improve outcomes in patients with very advanced (stage IIIb) cardiac immunoglobulin light chain amyloidosis

Limited utility of Mayo 2012 cardiac staging system for risk stratification of patients with advanced cardiac AL amyloidosis - analysis of a uniformly treated cohort of 1,275 patients

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