Prevalence and prognostic value of conduction disturbances at the time of diagnosis of cardiac AL amyloidosis. (Q47952949)

PubMed ID

23879272

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23879272%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

title

Prevalence and prognostic value of conduction disturbances at the time of diagnosis of cardiac AL amyloidosis (English)

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13 May 2020

7

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13 May 2020

Giampaolo Merlini

8

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13 May 2020

Roberta Mussinelli

3

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13 May 2020

Stefano Perlini

9

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13 May 2020

author name string

Michele Boldrini

1

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13 May 2020

Francesco Salinaro

2

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13 May 2020

Ambra Raimondi

4

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13 May 2020

Alessio Alogna

5

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13 May 2020

Francesco Musca

6

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13 May 2020

publication date

20 January 2013

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PubMed ID

23879272

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23879272%20AND%20SRC:MED&resulttype=core&format=json

Annals of Noninvasive Electrocardiology

5 March 2020

published in

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13 May 2020

volume

18

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13 May 2020

issue

4

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13 May 2020

page(s)

327-335

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Molecular mechanisms of amyloidosis

13 May 2020

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Diagnosis and management of the cardiac amyloidoses

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Dangerous small B-cell clones.

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Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant

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Significance of a fragmented QRS complex versus a Q wave in patients with coronary artery disease.

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Prognostic value of fragmented QRS in cardiac AL amyloidosis

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Amyloid heart disease

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Simple criteria for differentiation of Fabry disease from amyloid heart disease and other causes of left ventricular hypertrophy

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Serum N-terminal pro-brain natriuretic peptide is a sensitive marker of myocardial dysfunction in AL amyloidosis.

21 January 2018

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Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: a staging system for primary systemic amyloidosis

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Survival in patients with primary systemic amyloidosis and raised serum cardiac troponins

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The combination of high-sensitivity cardiac troponin T (hs-cTnT) at presentation and changes in N-terminal natriuretic peptide type B (NT-proBNP) after chemotherapy best predicts survival in AL amyloidosis.

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Importance of the echocardiographic evaluation of right ventricular function in patients with AL amyloidosis.

21 January 2018

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Right ventricular function in AL amyloidosis: characteristics and prognostic implication

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Best use of cardiac biomarkers in patients with AL amyloidosis and renal failure.

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Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms

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Midwall mechanics are improved after regression of hypertensive left ventricular hypertrophy and normalization of chamber geometry.

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Out-of-hospital cardiac arrest in patients with cardiac amyloidosis: presenting rhythms, management and outcomes in four patients.

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Gross anatomy of the human cardiac conduction system with comparative morphological and developmental implications for human application

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Clinically significant cardiac amyloidosis

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New pathological insights into cardiac amyloidosis: implications for non-invasive diagnosis

21 January 2018

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Amyloid cardiomyopathy in systemic non-hereditary amyloidosis. Clinical, echocardiographic and electrocardiographic findings in 30 patients with AA and 24 patients with AL amyloidosis

21 January 2018

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12 December 2020

A phase II trial of cyclophosphamide, lenalidomide and dexamethasone in previously treated patients with AL amyloidosis.

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12 December 2020

Symptomatic conduction system disease in cardiac amyloidosis

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Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective.

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Cardiac amyloidosis: a treatable disease, often overlooked

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Recognition and significance of intraventricular block due to myocardial infarction (peri-infarction block)

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12 December 2020

Amyloidosis (AL). Clinical and laboratory features in 229 cases

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Midwall left ventricular mechanics. An independent predictor of cardiovascular risk in arterial hypertension

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Cardiac amyloidosis causing cardiac dysfunction: analysis of 54 necropsy patients

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Cardiac arrhythmias in systemic amyloidosis: correlation with echocardiographic abnormalities

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Non-invasive predictors of survival in cardiac amyloidosis

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Comparison of electrocardiographic findings in patients with AL (primary) amyloidosis and in familial amyloid polyneuropathy and anginal pain and their relation to histopathologic findings

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Identifiers

DOI

10.1111/ANEC.12032

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6932035&resulttype=core&format=json

13 May 2020

1 reference

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13 May 2020

1 reference