Results 21 to 30 of about 49,586 (211)

Transthyretin derived amyloid deposits in the atrium and the aortic valve: insights from multimodality evaluations and mid-term follow up

open access: yesBMC Cardiovascular Disorders, 2023
Background Recent studies have reported atrial involvement and coexistence of aortic stenosis in transthyretin (ATTR) cardiac amyloidosis (CA). However, pathological reports of extraventricular ATTR amyloid deposits in atrial structures or heart valves ...
Atsushi Okada   +14 more
doaj   +1 more source

Using attribute construction to improve the predictability of a GP financial forecasting algorithm [PDF]

open access: yes, 2013
Financial forecasting is an important area in computational finance. EDDIE 8 is an established Genetic Programming financial forecasting algorithm, which has successfully been applied to a number of international datasets. The purpose of this paper is to
Kampouridis, Michael   +1 more
core   +1 more source

Multimodality assessments of wild‐type transthyretin cardiac amyloidosis with no ventricular hypertrophy

open access: yesESC Heart Failure, 2023
While patients with transthyretin cardiac amyloidosis (ATTR‐CA) typically present with concentric or asymmetric hypertrophy, a small percentage of ATTR‐CA is known to present with ‘atypical’ cardiac morphologies such as eccentric hypertrophy or even no ...
Takuma Iwaya   +6 more
doaj   +1 more source

Assessment and Management of Older Patients With Transthyretin Amyloidosis Cardiomyopathy: Geriatric Cardiology, Frailty Assessment and Beyond

open access: yesFrontiers in Cardiovascular Medicine, 2022
Transthyretin amyloidosis cardiomyopathy (ATTR-CM) is commonly diagnosed in older adults, in particular the wild-type (ATTRwt), which is regarded as an age-related disease.
Biobelemoye Irabor   +4 more
doaj   +1 more source

Val122Ile mt-ATTR Has a Worse Survival Than wt-ATTR Cardiac Amyloidosis

open access: yesJournal of the American College of Cardiology, 2017
Maurer et al. [(1)][1] reported results from the THAOS (Transthyretin Amyloid Outcome Survey) registry of transthyretin cardiac amyloid (ATTR) amyloidosis, in which they compared differences between patients carrying wild-type ATTR (wt-ATTR) cardiac amyloidosis and those carrying the mutant ...
Avinainder, Singh   +2 more
openaire   +2 more sources

Nationwide prevalence and characteristics of transthyretin amyloid cardiomyopathy in Sweden

open access: yesOpen Heart, 2021
Objective Transthyretin amyloid cardiomyopathy (ATTR-CM) is a rare, progressive and fatal condition caused by deposition of transthyretin amyloid fibrils in the heart.
J Gustav Smith   +9 more
doaj   +1 more source

Phage inducible islands in the gram-positive cocci [PDF]

open access: yes, 2016
The SaPIs are a cohesive subfamily of extremely common phage-inducible chromosomal islands (PICIs) that reside quiescently at specific att sites in the staphylococcal chromosome and are induced by helper phages to excise and replicate.
A Bolotin   +47 more
core   +1 more source

Temporal Stream Algebra [PDF]

open access: yes, 2012
Data stream management systems (DSMS) so far focus on event queries and hardly consider combined queries to both data from event streams and from a database.
Brodt, Simon, Bry, François
core   +4 more sources

ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable

open access: yesOrphanet Journal of Rare Diseases, 2021
Background The global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causing the ongoing coronavirus disease 2019 (COVID-19) pandemic has raised serious concern for patients with chronic disease.
Thomas H. Brannagan   +26 more
doaj   +1 more source

Prevalence of anxiety and depression symptoms in a sample of outpatients with ATTR cardiac amyloidosis

open access: yesFrontiers in Psychology, 2023
Patients with ATTR cardiac amyloidosis (ATTR-CA) face rare disease that could negatively influence psychological well-being with consequences on the course of the disease and quality of life.
Martina Smorti   +16 more
doaj   +1 more source

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