Cardiac amyloidosis: the great pretender (Q38372860)

2 September 2017

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title

Cardiac amyloidosis: the great pretender (English)

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2 September 2017

1

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5 June 2020

Massimiliano Lorenzini

2

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5 June 2020

author name string

Simone Longhi

3

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5 June 2020

Agnese Milandri

4

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5 June 2020

Christian Gagliardi

5

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5 June 2020

Ilaria Bartolomei

6

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5 June 2020

Fabrizio Salvi

7

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5 June 2020

Mathew S Maurer

8

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5 June 2020

publication date

1 March 2015

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2 September 2017

Heart Failure Reviews

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5 June 2020

volume

20

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5 June 2020

page(s)

117-124

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5 June 2020

issue

2

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https://scigraph.springernature.com/pub.10.1007/s10741-015-9480-0

5 June 2020

exact match

0 references

cites work

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21 January 2018

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THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis.

21 January 2018

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The Transthyretin Amyloidosis Outcomes Survey (THAOS) registry: design and methodology

21 January 2018

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Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type I in Póvoa do Varzim and Vila do Conde (north of Portugal).

21 January 2018

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Guideline of transthyretin-related hereditary amyloidosis for clinicians.

21 January 2018

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Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans

21 January 2018

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The amyloidogenic V122I transthyretin variant in elderly black Americans

21 January 2018

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Transthyretin-related amyloidoses and the heart: a clinical overview

21 January 2018

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

21 January 2018

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21 January 2018

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Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis.

21 January 2018

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Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases.

21 January 2018

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Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis

21 January 2018

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Diagnosis and management of the cardiac amyloidoses

21 January 2018

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Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types.

21 January 2018

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Prevalence and prognostic significance of low QRS voltage among the three main types of cardiac amyloidosis

21 January 2018

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Left ventricular structure and function in transthyretin-related versus light-chain cardiac amyloidosis.

21 January 2018

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Cardiovascular magnetic resonance in cardiac amyloidosis

21 January 2018

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Native T1 mapping in transthyretin amyloidosis

21 January 2018

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Role of cardiac magnetic resonance imaging in the detection of cardiac amyloidosis.

21 January 2018

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Quantification of myocardial extracellular volume fraction in systemic AL amyloidosis: an equilibrium contrast cardiovascular magnetic resonance study

21 January 2018

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(99m)Tc-pyrophosphate scintigraphy for differentiating light-chain cardiac amyloidosis from the transthyretin-related familial and senile cardiac amyloidoses

21 January 2018

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Defining the diagnosis in echocardiographically suspected senile systemic amyloidosis.

21 January 2018

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Proportion between wild-type and mutant protein in truncated compared to full-length ATTR: an analysis on transplanted transthyretin T60A amyloidosis patients

21 January 2018

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Strong transthyretin immunostaining: potential pitfall in cardiac amyloid typing

21 January 2018

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Usefulness and limitations of 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in the aetiological diagnosis of amyloidotic cardiomyopathy

21 January 2018

1 reference

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Utility and limitations of 3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in systemic amyloidosis

21 January 2018

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12 December 2020

Yield of Noncardiac Biopsy for the Diagnosis of Transthyretin Cardiac Amyloidosis

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12 December 2020

Amyloid cardiomyopathy: characterization by a distinctive voltage/mass relation

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12 December 2020

Pathophysiology and treatment of cardiac amyloidosis

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12 December 2020

Differential diagnosis of monoclonal gammopathy of undetermined significance

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12 December 2020

The myocardial contraction fraction is superior to ejection fraction in predicting survival in patients with AL cardiac amyloidosis

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12 December 2020

10.1007/S10741-015-9480-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25758359%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

1 reference