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Cutaneous Leishmaniasis Masquerading as Diabetic Foot: A Call for Vigilance.
Acta Dermatovenerol Croat
November 2024
Khalid Al Aboud King Faisal Hospital P.O Box 5440, Makkah, Saudi Arabia;
parts of the world (1,2). CL is characterized by significant clinical variability. An ulcerated nodule on the exposed parts of the body (corresponding to the parasite inoculation site by the vector insect) is the classic presentation.
View Article and Find Full Text PDFClinical and radiologic characteristics of ruptured epidermal inclusion cysts in the nipple and subareolar regions: A report of two cases.
Int J Gynaecol Obstet
December 2024
Obstetrics and Gynecology Department, Faculty of Medical Science, Lebanese University, Beirut, Lebanon.
Epidermal inclusion cysts (EICs) in the breast, particularly in the nipple and subareolar regions, are rare entities that pose significant diagnostic challenges and management dilemmas in clinical practice. This study retrospectively analyzes two case reports of women presenting with EICs located in these unusual breast areas. The subjects included a 35-year-old female with congested nipple symptoms and bilateral mastodynia, and a 58-year-old female with a palpable right breast nodule.
View Article and Find Full Text PDFThe motivation to inform others: a field experiment with wild chimpanzees.
PeerJ
December 2024
Budongo Conservation Field Station, Masindi, Uganda.
Background: Accumulating evidence indicates that some ape species produce more alarm behaviors to potential dangers when in the presence of uninformed conspecifics. However, since previous studies presented naturalistic stimuli, the influence of prior experience could not be controlled for.
Method: To examine this, we investigated whether apes (wild chimpanzees of the Budongo Forest, Uganda) would communicate differently about a novel danger (an unusually large spider) depending on whether they were with an uniformed conspecific.
Tupinicaris gen. nov. is proposed to accommodate a new hyporheic species of Parastenocarididae found in the northern portion of the Espinhaço mountain range (Minas Gerais, Brazil), in the Jequitinhonha River basin.
View Article and Find Full Text PDFAn analysis of mitochondrial variation in cardiomyopathy patients from the 100,000 genomes cohort: m.4300A>G as a cause of genetically elusive hypertrophic cardiomyopathy.
Hum Genomics
December 2024
Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, UK.
Article Synopsis
- A significant number of patients with cardiomyopathy have undetermined genetic causes, prompting researchers to analyze mtDNA variants in these cases through the 100,000 genomes project.
- The study scrutinized 1,363 genomes, identifying the pathogenic MT-TI m.4300A>G variant in four hypertrophic cardiomyopathy patients who had previously been undiagnosed, representing 0.6% of HCM cases without a known genetic cause.
- Findings suggest that MT-TI should be included in the initial genetic testing for non-syndromic hypertrophic cardiomyopathy to aid in diagnosing patients.
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