EXPRESS: Epidemiology, Diagnosis and Management of Cardiac Amyloidosis
Z Bashir, A Younus, S Dhillon, A Kasi… - Journal of …, 2024 - journals.sagepub.com
Cardiac amyloidosis (CA) is an infiltrative restrictive cardiomyopathy caused by the
deposition of amyloid fibrils in the myocardium. It manifests in two primary subtypes …
deposition of amyloid fibrils in the myocardium. It manifests in two primary subtypes …
[HTML][HTML] The Promising Role of Selenium and Yeast in the Fight Against Protein Amyloidosis
M Kieliszek, K Sapazhenkava - Biological Trace Element Research, 2024 - Springer
In recent years, increasing attention has been paid to research on diseases related to the
deposition of misfolded proteins (amyloids) in various organs. Moreover, modern scientists …
deposition of misfolded proteins (amyloids) in various organs. Moreover, modern scientists …
Morphological findings in different subtypes of hepatic amyloid
S Yasir, ZE Chen, C Hartley, L Zhang, M Torbenson - Human Pathology, 2024 - Elsevier
The classic findings have been well described for light-chain amyloid involving the liver. In
addition to light chain, however, many additional proteins are now known to be …
addition to light chain, however, many additional proteins are now known to be …
An ultra performance liquid chromatography method for transthyretin variants screening and heart failure assisting diagnosis
S Wang, L Guan, Y Sun, L Cui, S Guo, M Wang, Y Liu… - Clinica Chimica …, 2024 - Elsevier
Background Transthyretin (TTR) gene mutations are associated with hereditary amyloidosis
(ATTR) caused by mutant TTR protein dissociation, misfolding, aggregation, and insoluble …
(ATTR) caused by mutant TTR protein dissociation, misfolding, aggregation, and insoluble …
[HTML][HTML] Non-Cardiac Amyloidosis Findings Are Not Increased in African American Carriers of TTR V142I with Heart Failure and/or Arrhythmia
S Kaniper, D Lynch, SM Owens, L Ibric… - Journal of Personalized …, 2024 - mdpi.com
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a progressive systemic disease
involving the extracellular deposition of misfolded transthyretin protein. The hereditary …
involving the extracellular deposition of misfolded transthyretin protein. The hereditary …
[HTML][HTML] Gene-based therapies for neuromuscular disorders
E Zanoteli, MC França Jr… - Arquivos de Neuro …, 2024 - thieme-connect.com
Neuromuscular diseases (NMD) include a broad group of medical conditions with both
acquired and genetic causes. In recent years, important advances have been made in the …
acquired and genetic causes. In recent years, important advances have been made in the …
[PDF][PDF] RNA Interference Therapeutics for Hereditary Amyloidosis: A Narrative Review of Clinical Trial Outcomes and Future Directions
P Dave, P Anand, A Kothawala, P Srikaram, D Shastri… - Cureus, 2024 - cureus.com
Hereditary transthyretin amyloidosis (ATTR) is an autosomal dominant, life-threatening
genetic disorder caused by a single-nucleotide variant in the transthyretin gene. This …
genetic disorder caused by a single-nucleotide variant in the transthyretin gene. This …
Korunmuş Ejeksiyon Fraksiyonlu Kalp Yetersizliği Olan Hastalarda Kardiyak Amiloidoz Şüphesi için En Belirleyici Kırmızı Bayraklar The Most Predictive Red Flags for …
H Yalvaç, S MURAT, İ AK SİVRİKOZ… - … Dernegi arsivi: Turk …, 2024 - avesis.ogu.edu.tr
OBJECTIVE: Cardiac amyloidosis (CA) is a cardiomyopathy characterized by amyloid
infiltration in the myocardium. Transthyretin cardiac amyloidosis (TTR-CA), commonly …
infiltration in the myocardium. Transthyretin cardiac amyloidosis (TTR-CA), commonly …
[PDF][PDF] The Most Predictive Red Flags for Suspecting Cardiac Amyloidosis in Patients with Heart Failure with Preserved Ejection Fraction
KEFKY Olan, HKAŞ için En, BK Bayraklar - 2024 - jag.journalagent.com
Objective: Cardiac amyloidosis (CA) is a cardiomyopathy characterized by amyloid
infiltration in the myocardium. Transthyretin cardiac amyloidosis (TTR-CA), commonly …
infiltration in the myocardium. Transthyretin cardiac amyloidosis (TTR-CA), commonly …
[PDF][PDF] Expanding Options for Hereditary Transthyretin Amyloidosis with Polyneuropathy
V Bril, M Geneviève Matte - themedicalxchange.com
Background Amyloidosis is a term describing a heterogeneous array of acquired and
genetic disorders in which fibrillar proteins aggregate in target tissues to produce …
genetic disorders in which fibrillar proteins aggregate in target tissues to produce …