Results 181 to 190 of about 96,013 (363)
Fetal Cardiovascular Magnetic Resonance: History, Current Status, and Future Directions
Journal of Magnetic Resonance Imaging, Volume 61, Issue 6, Page 2357-2375, June 2025.Fetal cardiovascular magnetic resonance imaging (MRI) has emerged as a complementary modality for prenatal imaging in suspected congenital heart disease. Ongoing technical improvements extend the potential clinical value of fetal cardiovascular MRI.
Dominika Suchá +5 more
wiley +1 more source
Revista Colombiana de Cardiología, 2019 A bilateral persistent ductus arteriosus with right proximal pulmonary artery agenesis is a very unusual anatomic variant. These malformations are assumed to occur during the transformation of the sixth aortic arch with the pulmonary trunk in the ...
Esther Cambronero-Cortinas +4 more
doaj
Nomenclature of the ductus arteriosus [PDF]
Heart, 1983 M J Godman, R M Marquis
openaire +3 more sources
Rare but relevant: The injection of tablet preparations and pulmonary hypertension
Addiction, Volume 120, Issue 6, Page 1276-1279, June 2025.Abstract Intravascular injection of dissolved medicinal preparations such as crushed tablets is associated with a risk of injecting particulate material into the vasculature. This particulate material will naturally pass to the lungs where it will be largely filtered out in the pulmonary vascular bed, and in turn, it can result in a range of ...
Johan Duflou
wiley +1 more source
Expansion of the Phenotype of You‐Hoover‐Fong Syndrome and Possible Increased Risk of Cancer
American Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.ABSTRACT You‐Hoover‐Fong syndrome (YHFS) is a rare autosomal recessive disorder characterized by global developmental delay, microcephaly, dysmorphic facial features, and a spectrum of neurodevelopmental abnormalities. YHFS is caused by pathogenic variants in TELO2, a gene involved in regulation of the cell cycle. To date, 29 individuals with YHFS have
Alessandro De Falco +6 more
wiley +1 more source
Nonrecurrent Triplication of 5q21.3q23.3: A Case Report and Review of the Literature
American Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.ABSTRACT Triplications involving 5q21.3q23.3 are rare, and a phenotype has not been established. Here, we present a 4‐month‐old male with dysmorphic facial features and congenital cardiac malformation. Chromosomal microarray identified a pathogenic triplication of 5q21.3q23.3 with chromosome analysis showing the extra 5q material inserted into 16q ...
Jacob A. Ginter +5 more
wiley +1 more source
Effect of Site of Shunt on Left Heart-Volume Characteristics in Children with Ventricular Septal Defect and Patent Ductus Arteriosus [PDF]
, 1969 M. M. JARMAKANI +4 more
openalex +1 more source
American Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.ABSTRACT Primary Hypertrophic Osteoarthropathy (PHOAR1) is characterized by autosomal recessive loss of function variants in 15‐hydroxyprostaglandin dehydrogenase (HPGD) leading to digital clubbing, periostosis, pachydermia, and severe hyperhidrosis. HPGD catalyzes the first step of prostaglandin E2 (PGE2) degradation.
Kara Zehr +6 more
wiley +1 more source
Journal of Parenteral and Enteral Nutrition, Volume 49, Issue 4, Page 460-467, May 2025.Abstract Background Preterm infants are at risk of refeeding syndrome, a constellation of biochemical changes associated with nutrition. We aimed to determine whether increased early phosphate intake with routine biochemical monitoring is associated with a reduction in refeeding syndrome.
Thomas B. Wright +3 more
wiley +1 more source