The role of the laboratory in the diagnosis of cystic fibrosis
- 31 October 1984
- journal article
- research article
- Published by Elsevier in Clinical Biochemistry
- Vol. 17 (5) , 284-287
- https://doi.org/10.1016/s0009-9120(84)90553-8
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- PEPTIDASES IN AMNIOTIC FLUID: LOW VALUES IN CYSTIC FIBROSISThe Lancet, 1983
- α2-Macroglobulin in patients with obstructive lung disease, with and without α1-antitrypsin deficiencyClinica Chimica Acta; International Journal of Clinical Chemistry, 1983
- MICROVILLAR PEPTIDASE ACTIVITY IN AMNIOTIC FLUID: POSSIBLE USE IN THE PRENATAL DIAGNOSIS OF CYSTIC FIBROSISThe Lancet, 1983
- IMMUNOREACTIVE TRYPSIN SCREENING FOR CYSTIC FIBROSISActa Paediatrica, 1982
- Comparison of the diagnostic value of serum pancreatic isoamylase and immunoreactive trypsin measurement in patients with cystic fibrosis.Journal of Clinical Pathology, 1982
- Increased [125I]Trypsin-Binding in Serum from Cystic Fibrosis PatientsJournal of Pediatric Gastroenterology and Nutrition, 1982
- Serum immunoreactive trypsin in cystic fibrosis.Thorax, 1981
- SERUM-IMMUNOREACTIVE-TRYPSIN CONCENTRATIONS IN CYSTIC FIBROSISThe Lancet, 1979
- Decreased formation of α2-macroglobulin-protease complexes in plasma of patients with cystic fibrosisBiochemical and Biophysical Research Communications, 1976
- serum protein changes during the acute phase reactionClinica Chimica Acta; International Journal of Clinical Chemistry, 1969