Results 181 to 190 of about 135,106 (332)

Christmas Lights on the Heart: A Rare Case of Multiple Giant Coronary Artery Aneurysms

open access: hybrid
Giovanni Taverna   +8 more
openalex   +1 more source

Computational analysis to assess hemodynamic forces in descending thoracic aortic aneurysms

open access: yesThe Journal of Physiology, EarlyView.
Abstract figure legend Left: Pre‐processing. First, we perform the segmentation of the Computer Tomography angiorgraphy (angio‐CT) scans of a healthy patient, obtaining the surface of a healthy thoracic aorta with a Type III aortic arch. Then, we build nine ideal configurations with Descending Thoracic Aortic Aneurysm (DTAA), varying the aortic arch ...
Francesca Duca   +7 more
wiley   +1 more source

Case report: a clinical case of a giant coronary artery aneurysm treated by percutaneous exclusion. [PDF]

open access: yesEur Heart J Case Rep
D'Amato M   +4 more
europepmc   +1 more source

Impact of Partial Echo on 4D Flow MRI: The Insight From Synthetic MRI

open access: yesMagnetic Resonance in Medicine, Volume 95, Issue 6, Page 3462-3475, June 2026.
ABSTRACT Purpose The aim of this study is to investigate the impact of the partial echo on 4D flow MRI sequences thanks to in silico coupled MRI‐CFD (computational fluid dynamics) simulations. Methods Two sequences are studied: one with a full echo (FE) and another using partial echo (PE) with an echo symmetry fraction of 0.75.
Morgane Garreau   +6 more
wiley   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1098-1104, May 2026.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes   +3 more
wiley   +1 more source

Marfan Syndrome Associated With Intellectual Disability and Behavioral Anomalies: Further Evidence for the Effect of Compound Heterozygous Variants in FBN1 on Phenotypic Severity

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1021-1035, May 2026.
ABSTRACT Marfan syndrome (MFS) is a rare connective tissue disorder characterized by involvement of the cardiovascular, ocular, and musculoskeletal systems. Pathogenic variants in FBN1 cause most of the MFS cases; however, intellectual disability (ID) is rarely observed. A non‐consanguineous Pakistani family with four affected individuals was recruited.
Azmatullah Khan   +4 more
wiley   +1 more source

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