Results 151 to 160 of about 40,057 (294)
Cardiac hemangioma of the right atrium in a neonate : fetal management and expedited surgical resection [PDF]
Cardiac hemangioma is a rare tumor with a reported incidence of 1-2%. We describe the case of a neonate with a right atrial mass that was diagnosed prenatally. The fetus developed a supraventricular tachycardia and was delivered by cesarean section in
Campbell, A.+5 more
core +1 more source
F130The importance of the fetal echocardiography in nonimmunological hydrops fetalis (analysis of the 156 cases) [PDF]
Piotr Kaczmarek+3 more
openalex +1 more source
Background and Purpose Autophagy is essential for cellular homeostasis, and its impairment contributes to cardiac hypertrophy. Modulating autophagy has shown potential in treating pathological hypertrophy. Prolylcarboxypeptidase (PRCP), a lysosomal enzyme that hydrolyzes angiotensin II to Ang1‐7, has an unclear role in cardiac autophagy and hypertrophy.
Fangchao Zhou+16 more
wiley +1 more source
Congenital long QT syndrome: A challenging diagnosis by fetal echocardiography. [PDF]
Santi AD, Restrepo M.
europepmc +1 more source
P119Usefulness fetal echocardiography in the prenatal diagnosis of Down Syndrome (analysis of the 40 cases) [PDF]
A. Krasoń+5 more
openalex +1 more source
Background and Purpose Hypoxic pulmonary hypertension (HPH) is a chronic disorder marked by irreversible pulmonary vascular remodelling (PVR) and pulmonary artery smooth muscle cell (PASMC) dysfunction. Astragaloside IV (AS‐IV), a natural saponin from Astragalus, shows potential in HPH management. This study explores AS‐IV's protective effect on PVR in
Rongzhen Ding+12 more
wiley +1 more source
Clinical utility of fetal echocardiography: an Egyptian center experience. [PDF]
Al-Fahham MM+3 more
europepmc +1 more source
F82Detailed three‐dimensional fetal echocardiography facilitated by an internet link [PDF]
G. D. Michailidis+3 more
openalex +1 more source
Unraveling the Role of WDR91: Case Report of a Previously Unrecognized Clinical Entity
A novel case is herein described to expand the genetic and clinical spectrum of WDR91 and characterize a previously unrecognized autosomal recessive neurodevelopmental disorder. WDR91 deficiency results in neuronal loss, cortical thinning, and impaired brain development.
Nikolaos M. Marinakis+14 more
wiley +1 more source