Results 71 to 80 of about 29,196 (216)
Diagnostic Yield of Post‐Mortem Fetal Micro‐CT for Thoracic Abnormalities
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 +5 more
wiley +1 more source
Young stroke patient with patent foramen ovale and intracranial stenosis—a case report
The prevalence of patent foramen ovale is approximately 20% in the global population. In patients under the age of 55 years, it has been proven as a cause of acute ischemic embolic stroke of otherwise undetermined source.
Domagoj Šunde +5 more
doaj +1 more source
Secondary stroke prevention: patent foramen ovale, aortic plaque, and carotid stenosis [PDF]
Stroke is the most debilitating cardiovascular event. It has a variety of causes that may be present simultaneously. In young or otherwise healthy people, the search for a patent foramen ovale (PFO) has become standard.
Diener, Hans C. +3 more
core
The clinical manifestation of DOLV was atypical. TTE has a relatively high diagnostic accuracy for DOLV in pediatric, which is very valuable for its early detection. ABSTRACT Double outlet left ventricle (DOLV) is a rare congenital cardiac anomaly in which both great arteries originate entirely or predominantly from the morphologic left ventricle.
Xu Zhu +6 more
wiley +1 more source
Bilateral thalamic stroke in patient with patent foramen ovale and hereditary thrombophilia [PDF]
Patent foramen ovale and hereditary thrombophilia are both known risk factors for ischemic stroke. Artery of Percheron is a rare anatomical variant in which vast areas of the midbrain and thalamus have a single source of blood supply.
M Yu Brovko +11 more
doaj +1 more source
CRPPA exon 6–9 deletion as a founder mutation in Chinese patients with dystroglycanopathy
Analysis of sixteen Chinese dystroglycanopathy patients reveals a founder mutation (CRPPA exon 6–9 deletion) in 25% of cases and expands the phenotypic spectrum from severe muscle‐eye‐brain disease to limb‐girdle muscular dystrophy. ABSTRACT Importance Dystroglycanopathies (DGPs) are a group of muscular dystrophies with abnormal glycosylation of ...
Jihang Luo +18 more
wiley +1 more source
Body position and oxygenation: An intriguing relationship
Dyspnea and hypoxemia are among the most common symptoms and signs that need to be assessed in clinical practice.This case illustrates how simple steps in history taking and physical examination can be crucial for diagnosis.We present a patient with ...
Patrícia Rodrigues +7 more
doaj +1 more source
Obstetric outcome in women with congenital heart disease: A nationwide cohort in Sweden
In this large national case–control study in women with congenital heart disease, we showed an increased likelihood of giving birth prematurely, by cesarean section, and having a small‐for‐gestational‐age neonate compared to matched controls. Abstract Introduction Survival and healthcare for patients with congenital heart disease have improved, and the
Frida Wedlund +10 more
wiley +1 more source
Aerospace medicine required controlled terrestrial models to investigate influences of altered atmosphere conditions, such as hypoxia, on human health and performance. These models could potentially be expanded to encompass disease conditions or treatment targets regulated through hypoxia or hypercapnia.
Titiaan E. Post +4 more
wiley +1 more source
Migraine and patent foramen ovale: exploring the association and a possible treatment option [PDF]
Migraine is a very common type of headache. With a prevalence of 10-12%, migraine ranks 19th among diseases causing worldwide morbidity. Number of studies have shown a high prevalence of patent foramen ovale (PFO) in patients with migraine, especially ...
Hasan, Muhammed Yaser
core +1 more source

