Results 121 to 130 of about 7,937 (220)

Amyloidosis in the cardiovascular system [PDF]

open access: yes, 2016
In the most industrialized countries with a high degree of urbanization (including Ukraine), the leading cause of morbidity and mortality is occupied by diseases of the cardiovascular system.
Getmans’ka, V.
core  

Transthyretin Amyloid Cardiomyopathy: Diagnosis and Management

open access: yesCurrent Cardiovascular Risk Reports
Abstract Purpose of Review This review examines the recent advances in transthyretin amyloid cardiomyopathy (ATTR-CM), focusing on evolving diagnostic strategies and emerging therapeutic interventions. We sought to analyze the current state of diagnostic modalities, evaluate newly approved disease-modifying therapies,
Anja Selland   +3 more
openaire   +1 more source

Pittsburgh compound B positron emission tomography detects cardiomyopathy in hereditary transthyretin amyloidosis patients with negative bone scintigraphy: a pilot study

open access: yesFrontiers in Nuclear Medicine
PurposeTo evaluate the effectiveness of positron emission tomography (PET) with [11C]-Pittsburgh Compound-B ([11C]PiB) for detecting transthyretin amyloid (ATTR) cardiomyopathy in patients with transthyretin gene (TTR) variants associated with reduced ...
Hendrea S. A. Tingen   +12 more
doaj   +1 more source

Prevalence of transthyretin amyloid cardiomyopathy in pacemaker patients

open access: yesESC Heart Failure
AbstractAimsTransthyretin amyloid cardiomyopathy (ATTR‐CM) is characterized by increased wall thickness, diastolic dysfunction and progressive heart failure symptoms. The disease may infiltrate the conduction system leading to conduction disturbances requiring an implantation of permanent cardiac pacemaker (PM), but the extent is unknown.
Aaseth, Eirik, Christiansen, Jon Runar
openaire   +4 more sources

Transthyretin Amyloid Cardiomyopathy

open access: yesJournal of the American College of Cardiology, 2019
Frederick L. Ruberg   +4 more
openaire   +1 more source

Tafamidis therapy in transthyretin amyloid cardiomyopathy: a narrative review from clinical trials and real-world evidence

open access: yesThe Egyptian Heart Journal
Background Amyloidosis is a heterogeneous group of disorders caused by the extracellular deposition of insoluble misfolded proteins, leading to end-organ damage.
Ikponmwosa Jude Ogieuhi   +11 more
doaj   +1 more source

Extracellular Vesicles in Cardiac Amyloidosis: From Pathogenesis to Clinical Applications

open access: yesDiagnostics
Cardiac amyloidosis is an infiltrative cardiomyopathy caused by extracellular deposition of misfolded proteins, most commonly immunoglobulin light chains (AL) or transthyretin (ATTR), with rarer forms occurring less frequently. AL amyloidosis arises from
Ashot Batikyan   +12 more
doaj   +1 more source

In silico studies on potential binding sites of amyloid inhibitor compounds on amyloid beta peptide [PDF]

open access: yes, 2012
The formation of structurally similar insoluble fibrillar protein aggregates, called amyloids, is known to cause several neuronal and non-neuronal degenerative diseases such as Alzheimer‟s disease, Parkinson‟s disease, Huntington‟s disease and Diabetes ...
Rudra, Sumon
core  

Transthyretin amyloid cardiomyopathy: The emerging role of cardiac amyloid imaging

open access: yesAnnals of the Academy of Medicine, Singapore, 2021
Sarah Ming Li, Tan   +7 more
openaire   +2 more sources

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