Zobrazeno 1 - 10
of 20
pro vyhledávání: '"K J, Gaskin"'
Publikováno v:
Pediatric Surgery International. 7:140-142
A 3-year- 8-month-old girl developed obstructive jaundice associated with stricture of the distal end of the common bile duct 7 months after blunt abdominal trauma. Ultrasonography, computerised tomography, and percutaneous trans-hepatic cholangiogra
Publikováno v:
European journal of clinical nutrition. 50(3)
To assess body protein and protein deposition in prepubertal children with phenylketonuria (PKU).Cross-sectional study with nested longitudinal cohort.A tertiary referral paediatric hospital.37 PKU patients (3.9-11.0 years) and 27 unselected healthy
Autor:
D. J. H. Cockayne, A. Gyory, David M. Hunt, K. J. Gaskin, D. Hunter, T. E. Bostrom, E. V. O'loughlin
Publikováno v:
Gastroenterology. 110(2)
BACKGROUND & AIMS: Cystic fibrosis transmembrane conductance regulator (CFTR) is an adenosine 3',5'-cyclic monophosphate-dependent chloride channel that is defective in cystic fibrosis. The aims of this study were to determine if defective apical chl
Publikováno v:
Anaesthesia and intensive care. 23(5)
The incidence of gastro-oesophageal reflux in children undergoing general anaesthesia has not previously been studied. One-hundred-and-twenty children (ASA Class 1–2) were studied intraoperatively using continuous oesophageal pH monitoring. The inc
Autor:
D L, Waters, S F, Dorney, M A, Gruca, H C, Martin, R, Howman-Giles, A E, Kan, M, De Silva, K J, Gaskin
Publikováno v:
Hepatology (Baltimore, Md.). 21(4)
Focal and multilobular biliary cirrhosis are considered pathognomonic of cystic fibrosis (CF) and almost invariably have been reported in patients with steatorrhea. In contrast, patients with pancreatic sufficiency and normal absorption are considere
Publikováno v:
European journal of clinical nutrition. 48(6)
To directly assess the body protein content of children with chronic renal failure (CRF) and short stature.A tertiary referral paediatric hospital.There were: (i) 17 patients (10 male, nine pre-pubertal; mean age 12.90 +/- 3.20 years) with CRF and he
Autor:
Donna Waters, I R J Humphries, David C K Roberts, K J Gaskin, A H Lipson, R G Howman-Giles, J R Allen
Publikováno v:
The American journal of clinical nutrition. 59(2)
Previous studies have suggested that children with phenylketonuria (PKU) have a reduction in bone mineralization compared with control subjects. To investigate this, bone mineral density (BMD) of the total body (TBMD) was measured in 32 prepubertal c
Publikováno v:
Australasian physicalengineering sciences in medicine. 16(3)
An indirect calorimeter was developed to measure resting energy expenditure (REE) and respiratory quotient (RQ) in a clinical paediatric population. The design is suitable for any child spontaneously breathing room air. Measurements are possible from
Publikováno v:
Basic life sciences. 60
Autor:
R. Smith, K. J. Gaskin, C. Bambach, D. Stiel, David M. Hunt, I. M. Bruzuszcak, H. C. O. Martin, E. V. O'loughlin
Publikováno v:
The American journal of physiology. 260(5 Pt 1)
Abnormal epithelial electrolyte transport has been identified in a range of cystic fibrosis (CF) organs and appears to account for the various clinical manifestations of the disease. The aim of this study was to further define the Cl- secretion defec