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Published in 2019 at "Clinical Research in Cardiology"
DOI: 10.1007/s00392-019-01467-1
Abstract: BackgroundCarpal tunnel syndrome (CTS) and spinal canal stenosis can be frequently observed in the medical history of patients with transthyretin amyloidosis (ATTR), both in the hereditary (mt-ATTR) and wild-type (wt-ATTR) form. The aim of this…
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Keywords:
canal stenosis;
spinal canal;
amyloidosis;
stenosis ... See more keywords
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Published in 2019 at "Journal of Cardiac Failure"
DOI: 10.1016/j.cardfail.2019.07.080
Abstract: Introduction Deposition of wild type or mutant transthyretin (TTR) amyloid fibrils causes TTR cardiac amyloidosis (ATTR-CA). Targeted therapeutics (TT) for ATTR-CA include TTR stabilizers (tafamidis, dilfunisal) and oligonucleotide drugs (Revusiran, Patisiran and Inotersen).TTR stabilizers prevent…
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Keywords:
targeted therapeutics;
patients attr;
therapeutics transthyretin;
cause mortality ... See more keywords
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Published in 2023 at "Europace"
DOI: 10.1093/europace/euad122.631
Abstract: Abstract Funding Acknowledgements Type of funding sources: None. Background/Introduction Transthyretin cardiac amyloidosis (ATTR-CA) is associated with an increased incidence of arrhythmias. We hypothesized that non-invasive, two-week outpatient cardiac rhythm monitoring of patients with ATTR-CA would…
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Keywords:
patients attr;
two week;
cardiac amyloidosis;
transthyretin cardiac ... See more keywords
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Published in 2021 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-021-01706-7
Abstract: Background Transthyretin amyloidosis, or ATTR, is a progressive and debilitating rare proteopathy generally manifested as either transthyretin amyloid polyneuropathy (ATTR-PN) or transthyretin amyloid cardiomyopathy (ATTR-CM). Irrespective of the clinical presentation, affected patients manage a chronic…
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Keywords:
polyneuropathy attr;
family;
transthyretin amyloid;
attr ... See more keywords