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Klin Padiatr ; 195(1): 24-8, 1983.
Article in German | MEDLINE | ID: mdl-6834734

ABSTRACT

Its objectivity and reproducibility having been checked by for independent researchers, the Chrispin-Norman score has proved to be a useful yardstick for evaluating pulmonary changes in cystic fibrosis. The correlation to arterial pO2 was r = 0.68, and to the Schwachman-Kulczycki score, r = 0.75. Scores still consistent with a good general clinical condition were 10.5 in patients under 8 years of age; 13.4 in patients aged between 8 and 13; and 15.5 in the 13-20 age group. An average increase of more than 2 points a year indicates a particularly high danger level.


Subject(s)
Cystic Fibrosis/diagnostic imaging , Lung/diagnostic imaging , Adolescent , Adult , Child , Child, Preschool , Cystic Fibrosis/classification , Female , Humans , Infant , Male , Prognosis , Radiography
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