Results 131 to 140 of about 306,357 (278)

A Deep Learning Model for Coronary Artery Segmentation and Quantitative Stenosis Detection in Angiographic Images [PDF]

open access: yesarXiv
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

open access: yesJournal of Pediatric Surgery Case Reports, 2018
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

open access: yesSAGE Open Medical Case Reports
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]

open access: yesInt J Surg Case Rep, 2023
Bienfait MM   +5 more
europepmc   +1 more source

Minimally invasive approach to non-communicating pyloric duplication

open access: yesJournal of Pediatric Surgery Case Reports, 2018
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  

MIRAGE syndrome: a case report of de novo SAMD9 c.884del p.(Pro295GlnfsTer104) variant and a novel phenotype of pyloric stenosis

open access: yesEgyptian Journal of Medical Human Genetics
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

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