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pro vyhledávání: '"Peter Tormey"'
Autor:
Peter Tormey
Publikováno v:
Don't Forget The Bubbles.
Autor:
Peter Tormey
Publikováno v:
Don't Forget The Bubbles.
Publikováno v:
Abstracts.
Introduction Paediatricians play a significant role in preventive healthcare1. There is a strong link between radiation exposure and the development of cancer2. The typical dose of radiation required for an abdominal x-ray (AXR) is 0.46 mSv, which is
Publikováno v:
Abstracts.
Background Children with autism and complex needs are frequently seen in the Emergency Department (ED). This can be extremely distressing experience for them. This experience can be improved by several measures, including: staff who are experienced i
Publikováno v:
Abstracts.
Introduction The high-risk, low-volume nature of paediatric emergencies can results in a lack of physician comfort and confidence in dealing with sick children.1 Simulation training can help improve caregiver confidence and team communication and per
Autor:
I Okafor, Nandini Kandamany, Orla Callender, Tracey McCrudden, Patrick Fitzpatrick, Peter Tormey, R McNamara
Publikováno v:
Abstracts.
Introduction Ankle injuries are common in children (∼ 2% of presentations to PEDs) 1 X-rays are ordered for 85–95% of patients but only 12% of x-rays reveal a fracture.1 Clinical prediction rules such as The Low Risk Ankle Rule (LRAR) exist to he
Autor:
Richard J. Simpson, Geraint Florida-James, Mark Ross, Lesley A Ingram, Eva Malone, Peter Tormey
Publikováno v:
Experimental Physiology. 101:1253-1264
What is the central question of the study? Are CD31+ angiogenic T (TANG ) cells preferentially mobilized in response to acute exercise? What is the main finding and its importance? Our study reveals that TANG cells are redistributed into the circulat
Publikováno v:
European Journal of Medical Genetics. 60:217-219
Pai Syndrome is a rare congenital malformation syndrome of unknown cause with hypertelorism, midline cleft lip, nasal and facial polyps, ocular anomalies and the presence of distinctive lipomas adjacent to the corpus callosum. Herein, we present an i
Pai Syndrome is a rare congenital malformation syndrome of unknown cause with hypertelorism, midline cleft lip, nasal and facial polyps, ocular anomalies and the presence of distinctive lipomas adjacent to the corpus callosum. Herein, we present an i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::bdae9050f37f0356fee4af82d98611bc
https://www.bib.irb.hr/1078203
https://www.bib.irb.hr/1078203
Publikováno v:
Experimental physiology. 101(4)