English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Plus monthly

Global: Zendy Tools annual

Global: Zendy Tools monthly

Global: Zendy Free Plan

2017;12(4):136. CroEcho 2017 Introduction: Amyloidosis is an infiltrative disease characterized by extracellular deposition of insoluble fibrillary protein. There are two major types: light-chain (AL) amyloidosis and transthyretinrelated cardiac amyloidosis (ATTR, mutant and wild type). Cardiac involvement can lead to restrictive cardiomyopathy (CMP) and heart failure. 99mTc-Pyrophosphate (99mTc-PPY) has high affinity for TTR amyloid, allowing differential diagnosis with AL and other nonamyloidotic CMP with hypertrophic phenotype, in which 99mTc-Pyrophosphate (PYP) is low or absent.1-4

Nuclear medicine imaging with 99mTc-Pyrophosphate scintigraphy in patients with suspected cardiac amyloidosis