Results 101 to 110 of about 615,985 (187)

Multiple cardiac malformations in a calf

open access: yesAustralian Veterinary Journal, Volume 104, Issue 11, Page 777-781, November 2026.
This paper describes the morphopathological aspects of a case of multiple cardiac malformations in a calf. A two‐day‐old male calf of undefined breed was born with an ectopic heart, presenting with dyspnoea and in lateral recumbency. The owner had repositioned the exposed heart beneath the adjacent skin, which was suclosed, without additional incisions
LA Soares   +7 more
wiley   +1 more source

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas–Mexico Border

open access: yesClinical Genetics, Volume 110, Issue 5, Page 627-636, November 2026.
Project GIVE provided evaluations and genome sequencing to 23 children with hearing loss along the Texas–Mexico border. Seventy percent received a molecular diagnosis and 56% of those diagnosed had changes to medical management. In this region, underdiagnosis of genetic hearing loss is due to care barriers rather than lower genetic burden.
Desiree Lanehart   +17 more
wiley   +1 more source

Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1

open access: yesClinical Genetics, Volume 110, Issue 5, Page 574-583, November 2026.
Integrating trio‐based genomic sequencing with detailed clinical evaluation across seven French–Vietnamese heterotaxy cases alongside a review of 108 published patients reveals strong genotype–phenotype correlations. Variants in DNAH9, PKD1L1, MMP21, and GDF1 define a broad spectrum from isolated situs inversus to complex conotruncal heart defects and ...
Thi Bich Tuyen Ho   +23 more
wiley   +1 more source

Total endovascular aortic arch repair: a comprehensive review comparing parallel graft techniques and custom-made devices

open access: yesAngiologia e Cirurgia Vascular
INTRODUCTION: Endovascular approaches have emerged as promising alternatives for treating aortic arch pathology, particularly in high-risk patients. This review provides a comprehensive analysis of total endovascular aortic arch reconstruction, focusing ...
Patrícia Carvalho   +8 more
doaj   +1 more source

Incidence of Intensive Care Unit Delirium After Heart Surgery: A Feasibility Study of a Forest Environment Intervention

open access: yesNursing in Critical Care, Volume 31, Issue 6, November 2026.
ABSTRACT Background Postoperative delirium is a serious complication in intensive care units (ICUs), particularly following cardiac surgery. It is associated with circadian rhythm disruption, sleep disturbances and adverse outcomes. ICU environments often lack natural time cues, which may exacerbate circadian misalignment and increase delirium risk ...
Jolana Wagner‐Skacel   +18 more
wiley   +1 more source

The python aortic arch

open access: yes, 2019
\ua9 2019 Cambridge University Press. Aortic arch anomalies are rare congenital cardiovascular malformations.
Magdum AK, Pawar RS, Anderson RH
core   +2 more sources

Case Report A Case of Elderly-Onset Ulcerative Colitis with Large-Vessel Giant Cell Arteritis Treated Successfully with Tofocitinib

open access: yesInflammatory Intestinal Diseases
Introduction: Large vessel vasculitis, including Takayasu arteritis and giant cell arteritis (GCA), is a recognized extraintestinal manifestation of ulcerative colitis (UC), but its optimal management remains unclear.
Kotaro Mitsui   +4 more
doaj   +1 more source

Vascular Anomalies in Children Misdiagnosed with Asthma : Case series

open access: yesSultan Qaboos University Medical Journal, 2015
In most asthmatic children, inhaled steroids can relieve and control the symptoms of asthma. Persistent wheezing and respiratory symptoms in young children despite appropriate treatment may indicate other diagnostic considerations.
Hashim Javad   +6 more
doaj  

Current approach to genetic testing and genetic evaluation referrals for adults with congenital heart disease

open access: yesFrontiers in Genetics
BackgroundCongenital heart disease (CHD) is the most common congenital anomaly. Up to 33% have an identifiable genetic etiology. Improved medical and surgical management of CHD has translated into longer life expectancy and a rapidly growing population ...
Laura B. Oehlman   +15 more
doaj   +1 more source

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