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High-Sensitivity Cardiac Troponin T to Exclude Cardiac Involvement in TTR Variant Carriers and ATTRv Amyloidosis Patients

Journal of clinical medicine, 2024-01, Vol.13 (3), p.810

2024

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Detection of cardiac amyloidosis on routine bone scintigraphy: an important gatekeeper role for the nuclear medicine physician

The international journal of cardiovascular imaging, 2024-06, Vol.40 (6), p.1183-1192

2024

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Imaging cardiac innervation in hereditary transthyretin (ATTRm) amyloidosis: A marker for neuropathy or cardiomyopathy in case of heart failure?

Journal of nuclear cardiology, 2020-10, Vol.27 (5), p.1774-1784

2020

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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

The American journal of cardiology, 2018-01, Vol.121 (1), p.107-112

2018

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99mTc-aprotinin imaging in cardiac amyloidosis. Make an old tool new again?

Journal of nuclear cardiology, 2020-08, Vol.27 (4), p.1155-1157

2020

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Anaphylactic reaction caused by skin contact with the disinfectant chloramine‐T

Contact dermatitis, 2019-05, Vol.80 (5), p.321-322

2019

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Enhanced endothelium-dependent microvascular responses in patients with Wegener's granulomatosis

Journal of rheumatology, 2007-09, Vol.34 (9), p.1875

2007

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Causes of AA amyloidosis: a systematic review

Amyloid, 2020-01, Vol.27 (1), p.1-12

2020

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Tafamidis in patients with severe heart failure due to transthyretin amyloidosis cardiomyopathy: Improved long‐term survival

European journal of heart failure, 2023-11, Vol.25 (11), p.2065-2066

2023

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Heart failure with preserved ejection fraction, atrial fibrillation, and the role of senile amyloidosis

European heart journal, 2019-04, Vol.40 (16), p.1287-1293

2019

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ELISA-4-amyloid: diagnostic accuracy of an ELISA panel for typing the four main types of systemic amyloidosis in subcutaneous abdominal fat tissue samples

Amyloid, 2024-08, p.1-10

2024

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Is small artery elasticity decreased prior to intima-media thickening in patients with longstanding rheumatoid arthritis?

Journal of rheumatology, 2011-10, Vol.38 (10), p.2133-2140

2011

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Neurofilament light chain, a biomarker for polyneuropathy in systemic amyloidosis

Amyloid, 2021-01, Vol.28 (1), p.50-55

2021

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Prevalence of wild‐type transthyretin amyloidosis in a prospective heart failure cohort with preserved and mildly reduced ejection fraction: Results of the Amylo‐VIP‐HF study

European journal of heart failure, 2024-03, Vol.26 (3), p.695-698

2024

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Regression of Bone-Tracer Uptake in Cardiac Transthyretin Amyloidosis

Mayo Clinic proceedings, 2020-02, Vol.95 (2), p.417-418

2020

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The Prevalence and Management of Systemic Amyloidosis in Western Countries

Kidney diseases, 2016-04, Vol.2 (1), p.10-19

2016

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Pathophysiological pathways in patients with heart failure and atrial fibrillation

Cardiovascular research, 2022-08, Vol.118 (11), p.2478-2487

2022

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AA amyloidosis in a father and daughter as complication of PSTPIP1 -associated myeloid-related proteinemia inflammatory (PAMI) syndrome

Amyloid, 2024-03, Vol.31 (1), p.82-84

2024

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Time for new imaging and therapeutic approaches in cardiac amyloidosis

European journal of nuclear medicine and molecular imaging, 2019-07, Vol.46 (7), p.1402-1406

2019

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How well does liver span as part of the consensus criteria for liver involvement in AL amyloidosis perform?

Amyloid, 2023-10, Vol.ahead-of-print (ahead-of-print), p.1-3

2023

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Diagnostic performance of liver stiffness as marker of liver involvement in systemic immunoglobulin light chain (AL) amyloidosis

Annals of hematology, 2024-08

2024

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Longitudinal analysis of serum neurofilament light chain levels as marker for neuronal damage in hereditary transthyretin amyloidosis

Amyloid, 2024-06, Vol.31 (2), p.132-141

2024

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Small artery elasticity is decreased in patients with systemic lupus erythematosus without increased intima media thickness

Arthritis research & therapy, 2010-01, Vol.12 (5), p.R181-R181

2010

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

Amyloid, 2018-10, Vol.25 (4), p.227-233

2018

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A real-life cohort study of immunoglobulin light-chain (AL) amyloidosis patients ineligible for autologous stem cell transplantation due to severe cardiac involvement or advanced disease

Amyloid, 2020-04, Vol.27 (2), p.119-127

2020

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High-Sensitivity Cardiac Troponin T to Exclude Cardiac Involvement in TTR Variant Carriers and ATTRv Amyloidosis Patients

Detection of cardiac amyloidosis on routine bone scintigraphy: an important gatekeeper role for the nuclear medicine physician

Imaging cardiac innervation in hereditary transthyretin (ATTRm) amyloidosis: A marker for neuropathy or cardiomyopathy in case of heart failure?

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

99mTc-aprotinin imaging in cardiac amyloidosis. Make an old tool new again?

Anaphylactic reaction caused by skin contact with the disinfectant chloramine‐T

Enhanced endothelium-dependent microvascular responses in patients with Wegener's granulomatosis

Causes of AA amyloidosis: a systematic review

Tafamidis in patients with severe heart failure due to transthyretin amyloidosis cardiomyopathy: Improved long‐term survival

Heart failure with preserved ejection fraction, atrial fibrillation, and the role of senile amyloidosis

ELISA-4-amyloid: diagnostic accuracy of an ELISA panel for typing the four main types of systemic amyloidosis in subcutaneous abdominal fat tissue samples

Is small artery elasticity decreased prior to intima-media thickening in patients with longstanding rheumatoid arthritis?

Neurofilament light chain, a biomarker for polyneuropathy in systemic amyloidosis

Prevalence of wild‐type transthyretin amyloidosis in a prospective heart failure cohort with preserved and mildly reduced ejection fraction: Results of the Amylo‐VIP‐HF study

Regression of Bone-Tracer Uptake in Cardiac Transthyretin Amyloidosis

The Prevalence and Management of Systemic Amyloidosis in Western Countries

Pathophysiological pathways in patients with heart failure and atrial fibrillation

AA amyloidosis in a father and daughter as complication of PSTPIP1 -associated myeloid-related proteinemia inflammatory (PAMI) syndrome

Time for new imaging and therapeutic approaches in cardiac amyloidosis

How well does liver span as part of the consensus criteria for liver involvement in AL amyloidosis perform?

Diagnostic performance of liver stiffness as marker of liver involvement in systemic immunoglobulin light chain (AL) amyloidosis

Longitudinal analysis of serum neurofilament light chain levels as marker for neuronal damage in hereditary transthyretin amyloidosis

Small artery elasticity is decreased in patients with systemic lupus erythematosus without increased intima media thickness

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

A real-life cohort study of immunoglobulin light-chain (AL) amyloidosis patients ineligible for autologous stem cell transplantation due to severe cardiac involvement or advanced disease

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