Results 111 to 120 of about 60,446 (292)

A phenomap of TTR amyloidosis to aid diagnostic screening

ESC Heart Failure, Volume 12, Issue 2, Page 1113-1118, April 2025.
Abstract Cardiac amyloidosis due to transthyretin (ATTR) remains an underdiagnosed cause of cardiomyopathy. As awareness of the disease grows and referrals for ATTR increase, clinicians are likely to encounter more atypical forms of the condition in clinical practice.
Alexios S. Antonopoulos, Theodoros Tsampras, George Lazaros, Konstantinos Tsioufis, Charalambos Vlachopoulos   +4 more
wiley   +1 more source

Glycosaminoglycans and Fabry's disease

Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale, 2010
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Zinellu E, LEPEDDA, Antonio Junior, Cigliano A, DE MURO, Pierina, Fancellu L, Concolino D, DEIANA, Giovanni Andrea, Sestito S, Moricca MT, Sechi GP, FORMATO, Marilena   +10 more
openaire   +4 more sources

Causal correlations between inflammatory proteins and heart failure: A two‐sample Mendelian randomization analysis

ESC Heart Failure, Volume 12, Issue 2, Page 1374-1385, April 2025.
Abstract Aims Inflammation plays a critical role in both the development and progression of heart failure (HF), which is a leading cause of morbidity and mortality worldwide. However, the causality between specific inflammation‐related proteins and HF risk remains unclear.
Xian‐Guan Zhu, Gui‐Qin Liu, Ya‐Ping Peng, Li‐Ling Zhang, Xian‐Jin Wang, Liang‐Chuan Chen, Yuan‐Xi Zheng, Xue‐Jun Xiang, Rui Qiao, Xian‐He Lin   +9 more
wiley   +1 more source

Impact of ER stress and the unfolded protein response on Fabry disease

EBioMedicine
Summary: Fabry disease (FD) is a lysosomal storage disorder caused by pathogenic missense and nonsense variants in the α-galactosidase A (GLA) gene, leading to absent or reduced enzyme activity.
Malte Lenders, Elisa Rudolph, Eva Brand
doaj   +1 more source

Fabry-P\'erot Huygens' Metasurfaces: On Homogenization of Electrically Thick Composites

, 2019
Realization of the anomalous refraction effects predicted by Huygens' metasurfaces (HMS) have required tedious and time-consuming trial-and-error numerical full-wave computations.
Ariel Epstein (14356830), Sherman W. Marcus (14356824)   +1 more
core   +1 more source

ZnO Nanowires by Chemical Bath Deposition: A Review on Doping and Functional Devices

Electron, EarlyView.
This review reports the most recent and well‐established state‐of‐the‐art and scientific challenges related to the doping of ZnO nanowires by chemical bath deposition, encompassing native point and hydrogen‐related defects, as well as extrinsic dopants.
Clément Lausecker, Adrien Baillard, Estelle Appert, Vincent Consonni   +3 more
wiley   +1 more source

Interfacial and durability aspects of extrinsic Fabry-Perot interferometric sensors in carbon fibre composites [PDF]

, 2003
This thesis is concerned with the interfacial and durability aspects of Extrinsic Fabry- Perot Interferometric (EFPI) sensors embedded in carbon fibre reinforced composites.
Etches, J A
core  

Update on role of agalsidase alfa in management of Fabry disease

, 2011
Uma RamaswamiPaediatric Metabolic Unit, Cambridge University Hospitals, Cambridge, UKAbstract: Fabry disease (FD) is an X-linked lysosomal storage disorder that affects both men and women.
Uma Ramaswami
core   +2 more sources

Nanophotonic Biosensors and the Paradigm of Trans‐Scale Autonomous Bio‐Integrated Diagnostics for Addressing Health Complexities

Electron, EarlyView.
Physics‐driven advances in optical nanobiosensors for rapid, miniaturized, and point‐of‐care diagnostics for next‐generation decentralized and personalized healthcare based on sensor intelligence. ABSTRACT Public health emergencies and the escalating burden of chronic diseases necessitate a paradigm shift from centralized laboratory testing to rapid ...
Vishal Chaudhary, Harsh Sable, Sonu Sonu, Lakshita Phor, Reddicherla Umapathi, Pradeep Bhadola   +5 more
wiley   +1 more source

Arrhythmogenesis in Fabry Disease

Current Cardiology Reports
Abstract Purpose of Review Fabry Disease (FD) is a rare lysosomal storage disorder characterised by multiorgan accumulation of glycosphingolipid due to deficiency in the enzyme α-galactosidase A. Cardiac sphingolipid accumulation triggers various types of arrhythmias, predominantly ventricular arrhythmia, bradyarrhythmia,
Roy, Ashwin, Cumberland, Max J., O’Shea, Christopher, Holmes, Andrew, Kalla, Manish, Gehmlich, Katja, Geberhiwot, Tarekegn, Steeds, Richard P.   +7 more
openaire   +2 more sources