Results 181 to 190 of about 479,259 (314)
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
Testicular pain as an unusual presenting symptom of aortic coarctation: a case report and review of the literature. [PDF]
Basazinew E +6 more
europepmc +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
Delayed presentation of aortic coarctation as an aortic dissection: a case report. [PDF]
Fayisa S +5 more
europepmc +1 more source
Abstract Background and Purpose Noise pollution, particularly by aircraft, is a significant risk factor for cardiovascular disease. Aircraft noise activates stress response pathways in the brain, via the amygdala, the sympathetic nervous system and the hypothalamic–pituitary–adrenal axis.
Ivana Kuntić +25 more
wiley +1 more source
Late Complications After Aortic Coarctation Repair. [PDF]
Santoro A +4 more
europepmc +1 more source
A nano‐interception strategy disrupts pathogenic fibroblast–macrophage crosstalk in chronic heart failure. Scalable Prussian blue nanoparticles selectively sequester CCL2 via ultrahigh‐affinity binding, preventing CCR2+ macrophage recruitment and breaking a key fibro‐inflammatory circuit. This approach demonstrates robust efficacy in murine and porcine
Bo Chen +16 more
wiley +1 more source
Multimodality Imaging Approach in Diagnosis and Follow-Up of Aortic Coarctation in Adulthood. [PDF]
La Mura L +8 more
europepmc +1 more source
ABSTRACT A right‐sided aortic arch, a congenital anomaly of the aortic arch, was initially described by Fioratti and Aglietti in 1963. This condition, associated with formation of a vascular ring, can constrict mediastinal organs such as the trachea and esophagus.
Md. Deluwar Hussen +5 more
wiley +1 more source
Aortic Valve Stenosis and Insufficiency Combined With Aortic Coarctation. [PDF]
Hu T, Tu W, Li L.
europepmc +1 more source

