Results 41 to 50 of about 27,854 (260)

Case of reversible Mobitz type II atrioventricular block after the use of injectable antipsychotics

open access: yesClinical Case Reports, 2022
Although Mobitz type II atrioventricular block is typically an arrhythmia arising from a permanent organic disorder of the His‐Purkinje system, reversible factors should also be considered. Here, we report the association between a rare reversible Mobitz
Hisao Naono   +5 more
doaj   +1 more source

AI‐Assisted IoT‐Enabled ECG Monitoring: Integrating Foundational and Generative AI Tools for Sustainable Smart Healthcare—Recent Trends

open access: yesAI &Innovation, EarlyView.
ABSTRACT The rapid evolution of the Internet of Things (IoT) has significantly advanced the field of electrocardiogram (ECG) monitoring, enabling real‐time, remote, and patient‐centric cardiac care. This paper presents a comprehensive survey of AI assisted IoT‐based ECG monitoring systems, focusing on the integration of emerging technologies such as ...
Amrita Choudhury   +2 more
wiley   +1 more source

Transient severe conduction disturbances associated with ankylosing spondylitis

open access: yesJournal of Arrhythmia, 2019
A 46‐year‐old man presented with advanced and complete atrioventricular block. He was diagnosed with human leukocyte antigen‐B27‐positive ankylosing spondylitis (AS) and treated with nonsteroidal anti‐inflammatory drugs for AS.
Kuniyasu Ikeoka   +4 more
doaj   +1 more source

Cystic Tumor of the Atrioventricular Node Causing Rapid-Onset and Reversible Complete Heart Block

open access: yesJACC: Case Reports, 2023
Cystic tumors of the atrioventricular node are rare primary cardiac neoplasms, frequently reported as a postmortem diagnosis during autopsy. Despite their small size, they can present with complete heart block or sudden cardiac death.
Alejandro Velasco, MD   +4 more
doaj   +1 more source

Fatal heart block from intentional yew tree (Taxus baccata) ingestion: a case report [PDF]

open access: yes, 2019
© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org ...
Chan, Mark   +3 more
core   +2 more sources

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

Graves’ Disease Presenting with Complete Atrioventricular Block

open access: yesCase Reports in Endocrinology, 2020
Hyperthyroidism commonly causes tachyarrhythmias such as sinus tachycardia and atrial fibrillation. Impaired atrioventricular conduction is a very rare complication of hyperthyroidism.
Young Sil Eom, Pyung Chun Oh
doaj   +1 more source

Fetal Atrioventricular Heart Block [PDF]

open access: yesClinical Chemistry, 2014
As part of routine prenatal care, the obstetrician of a 25-year-old gravida 1, para 0 woman performed fetal heart-rate monitoring at 22 weeks gestational age. The fetal heart rate was 90 bpm, below the expected range of 120–160 bpm. This finding prompted a subsequent fetal ultrasound and echocardiogram.
Michael A, DiMaio, James D, Faix
openaire   +2 more sources

Prolongation of AV nodal refractoriness by Ruta graveolens in isolated rat hearts [PDF]

open access: yes, 2008
Objectives: To evaluate concentration-dependent effects of total extract of Rusta graveolens and its purified alkaloid fraction on the nodal basic and functional properties.
Golalipour, M.J.   +4 more
core  

Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle   +26 more
wiley   +1 more source

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