Results 131 to 140 of about 306,357 (278)
The Schorstein Lecture ON CONGENITAL PYLORIC STENOSIS: Delivered at the London Hospital, October, 1910 [PDF]
R. Hutchison
openalex +1 more source
Epidermolysis Bullosa With Pyloric Stenosis: A Novel Lethal Variant. [PDF]
Ghazzawi RA, Fatma A.
europepmc +1 more source
A Deep Learning Model for Coronary Artery Segmentation and Quantitative Stenosis Detection in Angiographic Images [PDF]
Coronary artery disease (CAD) is a leading cause of cardiovascular-related mortality, and accurate stenosis detection is crucial for effective clinical decision-making. Coronary angiography remains the gold standard for diagnosing CAD, but manual analysis of angiograms is prone to errors and subjectivity.
arxiv
Hypertrophic pyloric stenosis treated with co-administration of nitroglycerin and atropine sulfate
Hypertrophic pyloric stenosis (HPS) is a common infantile disease that causes a transit pyloric disorder. For the treatment of this disorder, intravenous atropine sulfate (AS) has been reported to be effective.
Yoko Shino+4 more
doaj
Successful management of pylorospasm with atropine in a failure-to-thrive neonate case report
Pylorospasm is an elusive diagnosis that can mimic the presentation of pyloric stenosis. There is limited discussion regarding its management in neonates with few case reports describing the use of antispasmodic agents.
Eric T Mendenhall+4 more
doaj +1 more source
Congenital infantile hypertrophic pyloric stenosis in preterm dizygotic twins infants diagnosed early: A case report. [PDF]
Bienfait MM+5 more
europepmc +1 more source
Minimally invasive approach to non-communicating pyloric duplication
Pyloric duplication is a rare subset of alimentary tract duplications that can present in a manner almost identical to hypertrophic pyloric stenosis.
Patrick T. Delaplain+2 more
doaj
Background MIRAGE syndrome is a rare multisystem disorder characterized by myelodysplasia, infection, growth restriction, adrenal hypoplasia, genital phenotypes, and enteropathy, resulting from mutations in the SAMD9 gene.
Mohamad M. Assker+5 more
doaj +1 more source