Zobrazeno 1 - 10
of 101
pro vyhledávání: '"R Kornfält"'
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 93(4)
PHYSICAL HEALTH SCREENING OF SCHOOL-CHILDREN Extended Health Care Responsibilities for School-nurses
Publikováno v:
Acta Paediatrica. 68:879-885
All 410 ten- and twelve-year-old children of a school district underwent two repeated physical examinations within the school services, the first by the school nurse, the second by the school doctor. The aim was to compare their assessments to see if
Publikováno v:
Acta Paediatrica. 92:1090-1095
To investigate the possibility of identifying children at risk for language impairment based on a new screening instrument to assess communication and language skills at 18 mo of age.At 18 mo, 58 children were assessed with a screening instrument for
Publikováno v:
Journal of Clinical Pharmacy and Therapeutics. 25:427-434
In a prospective, randomised, cross-over study including cystic fibrosis patients with indications for HIVAT (home intravenous antibiotic treatment) the prospect of pharmaceutical intervention was investigated. A comparison between the use of disposa
Autor:
C, Schaedel, I, de Monestrol, L, Hjelte, M, Johannesson, R, Kornfält, A, Lindblad, B, Strandvik, L, Wahlgren, L, Holmberg
Publikováno v:
Pediatric pulmonology. 33(6)
The severity of lung disease in cystic fibrosis (CF) may be related to the type of mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, and to environmental and immunological factors. Since pulmonary disease is the main de
Autor:
R Kornfält
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). Supplement. 89(434)
A survey of the programme for developmental surveillance in the Child Health Centres (CHCs) in Sweden was performed using a questionnaire administered to the Chief Medical Officers (CMO) of the Child Health Services. The questionnaire asked about met
Autor:
C, Schaedel, L, Hjelte, I, de Monestrol, M, Johannesson, H, Kollberg, R, Kornfält, L, Holmberg
Publikováno v:
Clinical genetics. 56(4)
Children with cystic fibrosis (CF) diagnosed by neonatal screening have a better nutritional development and other advantages compared with those in a nonscreened group. The two-tier immunoreactive trypsinogen (IRT)/DNA screening protocol has been fo
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 87(4)
We report a child with multiple target organ pseudohypoaldosteronism type 1 with frequent recurrent pulmonary infections caused by Pseudomonas aeruginosa and Pasteurella multocida and high levels of chloride in sweat, urine and nasal secretion. Repet
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 84(10)