Results 71 to 80 of about 146,730 (293)

Water‐Soluble Molecular Wires for Membrane Potential Imaging

open access: yesAngewandte Chemie, EarlyView.
Fully water‐soluble fluorescent rosamine‐based amphiphilic molecular wires were developed for imaging membrane potentials. The performance of the probes was evaluated in single cardiomyocytes, murine pituitary gland, and islets of Langerhans.
Mirna El Khatib   +9 more
wiley   +2 more sources

The genetic component of Brugada Syndrome

open access: yesFrontiers in Physiology, 2013
Brugada Syndrome (BrS) is a clinical entity first described in 1992. BrS is characterized by ST-segment elevations in the right precordial leads and susceptibility to ventricular arrhythmias and sudden cardiac death.
Morten Wagner Nielsen   +6 more
doaj   +1 more source

Use of a Calcium Chelating Agent(NaEDTA) in Cardiac Arrhythmias [PDF]

open access: bronze, 1959
Burton D. Cohen   +3 more
openalex   +1 more source

A Memristor‐Based Event‐Driven Reservoir Computing System for Cardiac Arrhythmia Detection

open access: yesAdvanced Intelligent Systems, EarlyView.
A low‐power, memristor‐assisted system is developed for real‐time arrhythmia detection in wearable electrocardiograph (ECG) monitoring. It integrates a level‐crossing encoder, a reservoir computing module, and a memristor crossbar to compress, process, and classify signals efficiently.
Hanrui Li   +2 more
wiley   +1 more source

A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease

open access: yesCase Reports in Medicine, 2009
Brugada syndrome (BrS) is a primary electrical heart disease, which can lead to sudden cardiac death. In older patients with BrS, the disease may coexist with ischaemic heart disease (IHD) and recent studies support a synergistic proarrhythmic effect of ...
Anders G. Holst   +9 more
doaj   +1 more source

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong   +16 more
wiley   +1 more source

The Expanding Clinical and Genetic Spectrum of Muscle Glycogen Storage Disease 0, (GSD0B)

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Glycogen storage disorders are a group of genetic disorders affecting glucose homeostasis in the body. Muscular glycogen stores are essential for liberating glucose for energy supply during bursts of activity and sustained muscle work. Muscle glycogen storage disease 0 (GSD0B) is associated with biallelic variants in GYS1 causing muscular ...
Sarah Donoghue   +16 more
wiley   +1 more source

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