Results 121 to 130 of about 315,210 (298)
Hemodynamic evaluation using four‐dimensional flow magnetic resonance imaging or computational fluid dynamics can identify a high‐risk phenotype in Kommerell's diverticulum, which is characterized by intradiverticular vortex formation, low wall shear ...
Kenji Sakakibara +14 more
doaj +1 more source
Long‐Term Quality of Life in 1777 Persons With Hodgkin Lymphoma and 6166 Matched Comparators
ABSTRACT Survival has improved substantially for patients with Hodgkin lymphoma (HL), but long‐term quality of life (QoL) remains incompletely understood. This was a Danish, nationwide, cross‐sectional study of QoL among persons with a diagnosis of HL matched 1:10 to general population comparators.
Sissel Johanne Godtfredsen +13 more
wiley +1 more source
Introduction: Computed tomography angiography of the aorta (CTAA) is the modality of choice for investigating aortic disease. Our aim was to evaluate the image quality, contrast enhancement and radiation dose of electrocardiograph (ECG)-triggered and non-
Ying Mei Wong +4 more
doaj +1 more source
Pathogenic PF4/Polyanion ELISA‐Negative Antibodies in HIT
ABSTRACT Background Platelet factor 4‐polyanion enzyme‐linked immunosorbent assays (ELISAs) are considered highly sensitive for diagnosing heparin‐induced thrombocytopenia (HIT), such that current practice guidelines recommend use of ELISA‐negative results to exclude HIT.
Adam J. Kanack +25 more
wiley +1 more source
Optimizing Diagnostic Accuracy of Clinical Red Flags in RASopathies
ABSTRACT RASopathies are a group of genetic disorders caused by pathogenic variants in the RAS‐mitogen‐activated protein kinase (RAS–MAPK) signaling pathway, often presenting with congenital heart defects, craniofacial dysmorphisms, and developmental delays. To assess the diagnostic yield of genetic testing in patients with suspected RASopathies and to
Emanuele Bobbio +16 more
wiley +1 more source
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Acute type A aortic dissection (aTAAD) is a common aortic disease with a very high mortality rate. Due to its frequent involvement of vessels above aortic arch, it is highly prone to cause neurological complications.
WANG Jian⁃yu, BAI Yun⁃peng
doaj +1 more source
ABSTRACT Carpenter syndrome type 2 (CRPT2) is a rare autosomal recessive disease mainly characterized by craniosynostosis and polysyndactyly. CRPT2 is the rarer subtype of Carpenter syndrome (CRPTS) and is caused by biallelic variants in the multiple epidermal growth factor‐like domains 8 gene (MEGF8).
Kiana Rashidi +11 more
wiley +1 more source
Artificial intelligence in aortic CT angiography: current applications and future perspectives
Artificial intelligence (AI) is revolutionizing cardiovascular imaging, with aortic computed tomography angiography (CTA) emerging as a prominent area of application. CTA imaging is essential for the diagnosis, risk stratification, and treatment planning
Jingkai Xu +3 more
doaj +1 more source
8th International Meeting on Aortic Diseases. [PDF]
Elefteriades JA, Ziganshin BA.
europepmc +1 more source

