Results 171 to 180 of about 46,771 (265)

Serendipitous Supernormality

open access: yesAnnals of Noninvasive Electrocardiology, Volume 30, Issue 3, May 2025.
We describe supernormal conduction in a pattern of bigeminy or trigeminy due to serendipitous programming of the ventricular pacing rate at an exact factorial of the atrial flutter rate in a patient who underwent an ablate‐and‐pace strategy for recalcitrant atypical atrial flutter.
Behzad B. Pavri, Eitan Frankel
wiley   +1 more source

The 'Padua classification' of cardiomyopathies into three groups: hypertrophic/restrictive, dilated/hypokinetic, and scarring/arrhythmogenic. [PDF]

open access: yesEur Heart J Suppl
Corrado D   +17 more
europepmc   +1 more source

The Effect of Sacubitril/Valsartan on Supraventricular and Ventricular Arrhythmias in Patients With Heart Failure

open access: yesAnnals of Noninvasive Electrocardiology, Volume 30, Issue 3, May 2025.
Patients undergoing SV therapy had significantly less VTVF events and associated clinical interventions. This effect could lead to less possibility of lethal arrhythmia and sudden cardiac death. ABSTRACT Background Patients with heart failure with reduced ejection fraction (HFrEF) frequently experience electrical disturbances, such as ventricular or ...
Alireza Arzhangzadeh   +14 more
wiley   +1 more source

A case report of mixed left ventricular non-compaction/hypertrophic cardiomyopathy phenotype in a child. [PDF]

open access: yesEur Heart J Case Rep
Cirillo C   +4 more
europepmc   +1 more source

Chchd10: A Novel Metabolic Sensor Modulating Adipose Tissue Homeostasis

open access: yesAdvanced Science, Volume 12, Issue 15, April 17, 2025.
Chchd10 is a novel regulator of adipose tissue (AT) homeostasis upon excess energy intake. Rapid Chchd10 reduction in response to high‐fat diet induction promotes adipogenesis in subcutaneous AT to store excess energy. On the other hand, sustained Chchd10 reduction protects visceral AT from 4‐HNE‐induced adipocyte dysfunction, attenuating the ...
Xiaoping Wu   +11 more
wiley   +1 more source

An Extended Phenotype of PPP1R13L Cardiocutaneous Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 4, April 2025.
ABSTRACT Dilated cardiomyopathy (DCM) is a rare disease in children and a leading cause of heart failure. There are numerous causes of DCM including genetic causes leading to isolated or syndromic presentations, with a wide variety of implicated genes.
Alicia Coudert   +8 more
wiley   +1 more source

Dose‐related cardiac outcomes in response to postnatal dexamethasone treatment in premature lambs

open access: yesThe Anatomical Record, Volume 308, Issue 4, Page 1214-1228, April 2025.
Abstract Background Postnatal corticosteroids are used in the critical care of preterm infants for the prevention and treatment of bronchopulmonary dysplasia. We aimed to investigate the effects of early postnatal dexamethasone therapy and dose on cardiac maturation and morphology in preterm lambs.
Amanda Vrselja   +5 more
wiley   +1 more source

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