Salivary electrolyte concentrations are associated with cystic fibrosis transmembrane regulator genotypes

Clinical Chemistry and Laboratory Medicine

Volumn 40, Issue 4, 2002, Pages 345-350

  Aps, Johan K M ^a   Belanghe, Joris ^a   Martens, Luc C ^a  

^a Dept Paediatr Dent/Special Care ^*  (Belgium)

Author keywords

Caries; Cystic fibrosis; Electrolytes; Genotype; Saliva

Indexed keywords

BICARBONATE; CALCIUM ION; CHLORIDE ION; ELECTROLYTE; PHOSPHATE; POTASSIUM ION; SODIUM ION; TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR PROTEIN, HUMAN;

ADOLESCENT; ADULT; ARTICLE; BELGIUM; CHILD; CONTROLLED STUDY; CYSTIC FIBROSIS; DENTAL CARIES; DIAGNOSTIC KIT; GENE MUTATION; GENETIC CODE; GENETIC IDENTIFICATION; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; OSMOLARITY; PRIORITY JOURNAL; SALIVA LEVEL; STATISTICAL ANALYSIS; AGED; ANALYTICAL EQUIPMENT; GENETICS; HEALTH SURVEY; METABOLISM; MIDDLE AGED; MUTATION; PRESCHOOL CHILD; SALIVA;

ADOLESCENT; ADULT; AGED; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DENTAL CARIES; DMF INDEX; ELECTROLYTES; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MIDDLE AGED; MUTATION; OSMOLAR CONCENTRATION; REAGENT KITS, DIAGNOSTIC; SALIVA;

EID: 0036000770     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.2002.055     Document Type: Article

References (29)

1. Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patients
2. Differences in expression of cystic fibrosis in blacks and whites
3. Reaching the diagnosis of cystic fibrosis-the limits of the spectrum
4. Sweat testing following newborn screening for cystic fibrosis
5. Pancreatic function and extended mutation analysis in delta F508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels
6. What is cystic fibrosis diagnosis?
7. Diagnosis of cystic fibrosis
8. Normal sweat chloride values do not exclude the diagnosis of cystic fibrosis
9. Clinical spectrum in homozygotes and compound heterozygotes inheriting cystic fibrosis mutation 3849 + 10 kbC→T: Significance for geneticists
10. The significance of sweat CI/Na ratio in patients with borderline sweat test
11. The application of saliva, sweat and tear fluid for diagnostic purposes
12. The diagnostic uses of saliva
13. Increased salivary buffering in association with a low caries experience in children suffering from cystic fibrosis
14. Dental health of children with cystic fibrosis: An interim report
15. Dental health of patients suffering from cystic fibrosis in Northern Ireland
16. Cystic fibrosis: A current review
17. Sodium and chlorine concentrations in mixed saliva of healthy and cystic fibrosis children
18. Studies on dental caries: I. Dental status and dental needs of elementary schoolchildren
19. British Association for the Study of Community Dentistry (BASCD) guidance on the statistical aspects of training and calibration of examiners for surveys of child dental health. A BASCD co-ordinated dental epidemiology quality standard
20. British Association for the Study of Community Dentistry (BASCD) diagnostic criteria for caries prevalence surveys - 1996/7
21. Is oral health at risk in people with cystic fibrosis?
22. The mineral in tooth enamel and dental caries
23. Mutans streptococci, lactobacilli and caries experience in cystic fibrosis homozygotes, heterozygotes and healthy controls
24. Caries experience and oral cleanliness in cystic fibrosis homozygotes and heterozygotes
25. The influence of medication and dietary habits on caries experience and oral cleanliness in cystic fibrosis homozygotes
26. SDS-PAGE of salivary proteins in cystic fibrosis: Preliminary results