Results 61 to 70 of about 155,604 (313)

HFE-Mamba: High-Frequency Enhanced Mamba Network for Efficient Segmentation of Left Ventricle in Pediatric Echocardiograms

open access: yesIEEE Access
Automated ventricular function analysis can enhance healthcare consistency and accessibility, particularly in resource-limited settings. Current segmentation methods trained on adult heart ultrasounds struggle to accurately outline the irregular shape of
Zi Ye   +4 more
doaj   +1 more source

A known case of myocardial infarction and its outcome in pregnancy

open access: yesAPIK Journal of Internal Medicine, 2022
Acute myocardial infarction (AMI) is rare in women of child- bearing age during pregnancy. Its prevalence is 1/10,000–30,000. A 32-year-old primigravida, with a history of acute MI 1 year ago, presented to us with regular antenatal checkups and was ...
Veena M Vernekar   +6 more
doaj   +1 more source

Clinical Characteristics and Concordance of Anti‐MDA5 Antibodies: A Multicenter Australian Study

open access: yesArthritis Care &Research, EarlyView.
Objective In Australia, anti‐MDA5 antibodies are exclusively tested by a line immunoblot assay (LIA). The clinical concordance of an LIA‐positive anti‐MDA5 result is unclear. We aimed to describe the clinical features and determine the clinical concordance of patients with anti‐MDA5 antibodies. Methods Electronic records of a multisite cohort (patients
Syed B. Ali   +11 more
wiley   +1 more source

Cardiovascular health in pediatric patients with X-linked hypophosphatemia under two years of burosumab therapy

open access: yesFrontiers in Endocrinology
IntroductionX-linked hypophosphatemia (XLH) is caused by an inactivating mutation in the phosphate-regulating endopeptidase X-linked (PHEX) gene whose defective product fails to control phosphatonin fibroblast growth factor 23 (FGF23) serum levels ...
Avivit Brener   +15 more
doaj   +1 more source

Acute onset of refractory hypoxemia: A rare hemodynamic cause of dyspnea

open access: yesIndian Journal of Respiratory Care, 2019
Platypnea-orthodeoxia syndrome (POS) is a rare condition of positional dyspnea with hypoxemia that can pose a diagnostic challenge to clinicians. We report two cases of POS with different pathophysiologic triggers and similar clinical features.
Tommaso Valobra   +2 more
doaj   +1 more source

Anomalous aortic origin of coronary artery: For a challenging diagnosis, a transthoracic echocardiogram is recommended

open access: yesActa paediatrica, 2021
Anomalous aortic origin of a coronary artery (AAOCA), especially the interarterial course of the right or left coronary artery, predisposes paediatric patients to myocardial ischaemia.
Antimo Tessitore   +5 more
semanticscholar   +1 more source

When Biology Meets Medicine: A Perspective on Foundation Models

open access: yesAdvanced Intelligent Discovery, EarlyView.
Artificial intelligence, and foundation models in particular, are transforming life sciences and medicine. This perspective reviews biological and medical foundation models across scales, highlighting key challenges in data availability, model evaluation, and architectural design.
Kunying Niu   +3 more
wiley   +1 more source

Circulating Biomarkers and Cardiac Structure and Function in Rheumatoid Arthritis

open access: yesFrontiers in Cardiovascular Medicine, 2021
Background: Rheumatoid arthritis (RA) increases the risk for abnormalities of the cardiac structure and function, which may lead to heart failure (HF). Studying the association between circulating biomarkers and echocardiographic parameters is important ...
Masatake Kobayashi   +19 more
doaj   +1 more source

Detecting and Classifying Myocardial Infarction in Echocardiogram Frames With an Enhanced CNN Algorithm and ECV-3D Network

open access: yesIEEE Access
Myocardial infarction is a serious medical condition that requires prompt and accurate diagnosis for effective treatment. In this paper, we present a novel approach for detecting and classifying MI in echocardiogram frames using an enhanced CNN algorithm
S. Deepika, N. Jaisankar
semanticscholar   +1 more source

Expanded Phenotype Associated With an Intronic PPP1R12A Variant: A Case Report and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal dominant PPP1R12A‐related genitourinary and/or brain malformation syndrome is a recently described multisystem disorder caused by loss‐of‐function variants in the protein phosphatase 1 regulatory subunit 12a (PPP1R12A) gene. To date, 22 affected individuals have been reported with variable brain malformations and genitourinary ...
Emily M. Bland   +4 more
wiley   +1 more source

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