Results 81 to 90 of about 41,868 (235)

Emerging Upper Extremity Muscle Ultrasound Patterns as a Diagnostic Aid in TTN‐Related Myopathies

Muscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims Biallelic pathogenic variants in TTN cause rare forms of early‐onset myopathy, manifesting with variable severity, distribution, and progression of muscle weakness, often associated with respiratory insufficiency and potentially cardiomyopathy. The large size of TTN and phenotypic heterogeneity in TTN‐related myopathy (TTN‐RM)
Abigail Potticary, Meghan McAnally, Sandra Donkervoort, Carsten G. Bönnemann   +3 more
wiley   +1 more source

Patent foramen ovale

Zdravniški Vestnik, 2006
Background: Stroke is the third cause of mortality and leading cause of disability regarding the World Health Organization data. Cryptogenic stroke encompasses 40% of young adults with ischemic stroke.
Marjan Zaletel, Mirta Koželj, Tomaž Podnar, Polona Peternel   +3 more
doaj  

Diagnostic Yield of Post‐Mortem Fetal Micro‐CT for Thoracic Abnormalities

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This study aims to identify the imaging findings specifically for thoracic anomalies in 1200 Micro‐CT cases, independent of whether the abnormality contributed to the main diagnosis or cause of death. Method We analyzed 1200 Micro‐CT scans in an unselected, consecutive cohort between 2017 and 2024 to identify thoracic anomalies ...
Ian C. Simcock, Audrey Lamouroux, Susan C. Shelmerdine, J. Ciaran Hutchinson, Neil J. Sebire, Owen J. Arthurs   +5 more
wiley   +1 more source

Following the flow: in vivo imaging of fetal foramen ovale physiology using four-dimensional flow magnetic resonance imaging with doppler ultrasound gating

Radiology Case Reports
The foramen ovale (FO) is a vital conduit of the fetal circulation, directing oxygenated blood from the placenta through the right atrium to the left atrium and thus to the brain and viscera.
Jochen Gerstner Saucedo, MD, Takashi Fujiwara, PhD, Erin K. Englund, PhD, Sungho Park, PhD, Richard Friesen, MD, Lorna P. Browne, MD, Alex J. Barker, PhD   +6 more
doaj   +1 more source

How to facilitate ultrasound examination of the fetal heart: the 5‐4‐3‐2‐1 method

Ultrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT We propose a new standardized, systematic method of fetal cardiac screening, the step‐by‐step ‘5‐4‐3‐2‐1’ method. This method is based on understanding the cardiac structures through a process of navigating between the different recommended views during an abdominothoracic sweep, following a user‐friendly checklist to identify the main ...
M. Levy, B. Stos
wiley   +1 more source

Study of pterygospinous and pterygoalar bars in relation to foramen ovale in dry human skulls

National Journal of Clinical Anatomy, 2019
Background Anatomical knowledge of bony bridges around the foramen ovale may be helpful for diagnostic and invasive neurosurgical procedures like electroencephalogram analysis, trigeminal rhizotomy, biopsy of cavernous sinus tumors, and mandibular nerve ...
Arvind Kumar Singh, Richa Niranjan
doaj   +1 more source

Predictors of Brain Infarction in Pediatric Patients During Extracorporeal Membrane Oxygenation

Artificial Organs, EarlyView.
In 179 pediatric ECMO patients, brain infarction (BI) occurred in 28% and was linked to markedly higher 30‐day mortality. VA ECMO mode (vs. VV) and higher pre‐ECMO arterial lactate independently predicted BI, supporting standardized neuro‐monitoring and liberal early brain CT, especially for children on VA ECMO.
Riccardo Iacobelli, Thomas Fux, Sara Wood Schalling, Sarah Kopfer, Jonas Berner, Alexander Fletcher‐Sandersjöö, Lars Mikael Broman   +6 more
wiley   +1 more source

Patent foramen ovale and stroke: prognosis and treatment in young adults. [PDF]

, 2005
A patent foramen ovale (PFO) is found with increased frequency in patients with stroke of undetermined origin but the significance and therapeutic implications of this observation remain unclear.
Cramer, Steven C
core   +1 more source

Homozygous Loss‐of‐Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental Abnormalities

Clinical Genetics, EarlyView.
Biallelic SLC20A1 loss‐of‐function variant causes a previously unrecognized multisystem developmental disorder. We report the first homozygous case presenting with tetralogy of Fallot, renal agenesis, polydactyly, and growth impairment. Transcriptome analysis of patient‐derived fibroblasts suggests significant dysregulation of pathways critical for ...
Eugénie Koumakis, Céline Huber, Wendy Chung, Christine Leroy, Pauline Parisot, Regis Gaudin, Mohamad Zaidan, Valérie Cormier‐Daire, Gérard Friedlander, Yoel Hirsch   +9 more
wiley   +1 more source

Obstructing Chiari Network Facilitating Blood Flow Across a Patent Foramen Ovale Causing Hypoxia

JACC: Case Reports, 2020
A 36-year-old man with progressive dyspnea and hypoxia was found to have a large, partially fenestrated Chiari network accelerating blood flow through a patent foramen ovale with preservation of an embryonic right-to-left atrial flow pattern.
Rimmy Garg, MD, Tyler Wark, MD, John Dudley, MD, James Robertson, MD   +3 more
doaj   +1 more source