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The Lingering Threat: A Migratory Fish Bone Causing Delayed Cervical Foreign Body Granuloma.
Indian J Otolaryngol Head Neck Surg
February 2025
Aurelius Hospital Negeri Sembilan, Nilai, Negeri Sembilan Malaysia.
Fish bone ingestion is a common presenting complaint to the Otorhinolaryngology clinic. In majority of the cases, the removal of visualised impacted fish bones is fairly straightforward. However, diagnostic dilemma may arise in cases of migratory fish bones as initial examination may be unsuspecting.
View Article and Find Full Text PDFFall and rise of a threatened raptor: Unraveling long-term population dynamics with spatially explicit integrated models.
Ecol Appl
March 2025
Equip de Biologia de la Conservació, Departament de Biologia Evolutiva, Ecologia i Ciències Ambientals and Institut de Recerca de la Biodiversitat (IRBio), Universitat de Barcelona, Barcelona, Spain.
Population dynamics are governed by the so-called four BIDE processes: birth, immigration, death, and emigration. However, most population models fail to explicitly consider all four processes, which may hinder a comprehensive understanding of how and why populations change over time. The advent of Integrated Population Models (IPMs) and recent developments in spatial mark-recapture models have enabled deeper insights into demography and dispersal.
View Article and Find Full Text PDFFirst prenatal case of jumping-like translocations: unraveling complex chromosomal rearrangements.
Chromosome Res
March 2025
Department of Genetics and Reference Center for Developmental Disorders Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, 76000, Rouen, France.
Jumping translocations and jumping-like translocations constitute a rare category of complex chromosomal rearrangements, which are primarily observed in hematologic disorders and solid tumors. This study outlines a complex structural mosaic rearrangement involving a single recipient chromosome and three distinct donor chromosomes, with varying patterns of mosaicism observed across different cell lines. The rearrangement was confirmed by karyotyping, FISH, and array-CGH.
View Article and Find Full Text PDFUnraveling the Molecular and Clinical Consequences of an Intragenic TRIP12 Duplication Using Genomic and RNA Analyses.
Am J Med Genet A
March 2025
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Clark-Baraitser syndrome is a rare neurodevelopmental disorder associated with the E3 ubiquitin-protein ligase gene TRIP12. Using chromosomal microarray analysis (CMA), long-range PCR, breakpoint sequencing, and RNA analyses, we studied a 6-year-old female presenting with developmental delay, aggressive behavior, attention-deficit hyperactivity disorder, and mild dysmorphic features. CMA revealed a de novo ~87 kb copy-number variant (CNV) duplication at 2q36.
View Article and Find Full Text PDFTwists and turns: unraveling the mystery of ileosigmoidal knotting, a rare and intriguing acute intestinal obstruction (a report of 3 cases).
Pan Afr Med J
March 2025
General Surgery, Mohammed VI University Hospital Center of Marrakech, Marrakech, Morocco.
Among the rare and complex causes of acute intestinal occlusion: volvulus due to the ileosigmoid node. The latter is secondary to the terminal ileum which will wrap around the base of the sigmoid colon and its meso, resulting in the formation of a node. Its natural evolution is the ischemia of the ileum and sigmoid, necessitating prompt emergency surgical intervention as the primary treatment approach.
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