Results 151 to 160 of about 49,976 (250)

The multiform sonographic spectrum of arterial duct in right aortic arch. [PDF]

open access: yesInt J Cardiovasc Imaging, 2021
Chiappa E, Ridolfi C, Cordisco A.
europepmc   +1 more source

Australian Guideline for the Identification and Management of Hypertension in Children and Adolescents

open access: yes
Journal of Paediatrics and Child Health, EarlyView.
N. G. Larkins   +28 more
wiley   +1 more source

Evaluating Perfusion Quantification for Phase‐Resolved Functional Lung MRI Using Gaussian Filtering

open access: yesNMR in Biomedicine, Volume 39, Issue 11, November 2026.
Current PREFUL perfusion quantification uses a slice‐wise median for the maximal blood exchange fraction ΔS, limiting regional information. Gaussian filtering (σ = 1.5) ΔS in perfusion calculation adds regional information and improves intrascan and interscan repeatability while preserving global and voxel‐wise correlations with DCE‐derived pulmonary ...
Kirsten J. Schmidt   +7 more
wiley   +1 more source

What's Your Diagnosis? Large Mediastinal Mass in a Dog

open access: yes
Veterinary Clinical Pathology, EarlyView.
Rosane O. Cruz   +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

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