ABC
Il test del sudore
VALENTINA KIREN, LAURA TRAVAN, ELSA BARTH
Clinica Pediatrica, IRCCS “Burlo Garofalo”, Università di Trieste
Ottobre 2004 - pagg. 573 -577
Parole chiave
Classificazione MeSH
Bibliografia
1. Wallis C. Diagnosis of cystic fibrosis;
blood, sweat and tears. Arch Dis Child
1997;76:85-91.
2. NCCLS. Sweat testing: Sample collection and Quantitative Analysis: Approved Guideline- Second Edition. NCCLS document C34-A2 [ISBN 1-56238-407-4]. NCCLS, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania USA, 2000.
3. Baumer JH. “Evidence based guidelines for the performance of sweat test for the investigation of cystic fibrosis in UK. Arch Dis Child 2003;88:1126-7.
4. Rosenstein BJ, et al. “The diagnosis of cystic fibrosis: a Consensus Statement. J Pediatr 1998;132(4):589-95.
5. Cystic Fibrosis Foundation. The diagnosis of Cystic Fibrosis. Consensus Statement. Consensus Conference, 1996, VII: sect.1.
6. Rosenstein BJ, Zeitlin PL. Cystic fibrosis. Lancet 1998;351:277-82.
7. Mastella G. Fibrosi cistica. Da: Argomenti di Malattie respiratorie infantili. Pisa, Pacini editore, 1998:95-142.
8. Salvatore D, Marchetti F, D’Andrea N, Schiavo MV. La fibrosi cistica in Basilicata: aspetti epidemiologici, clinici ed assistenziali. Bollettino OER 2001;vol. 1:12-15.
9. Vazquez C, Azcarate MJ, Sojo A, et al. Results of the sweat test, carried out by 2 methods, for the diagnosis of cystic fibrosis. An Esp Pediatr 1987;26(1):33-6.
10. Webster HL. Laboratory diagnosis of cystic fibrosis. Crit Rev Clin Lab Sci 1983;18(4): 313-38.
11. Rosenstein BJ. What is a cystic fibrosis diagnosis? Clin Chest Med 1998;19(3):423-41.
12. Farrell PM, Koscik RE. Sweat chloride concentrations in infants homozygous or heterozygous for DF508 cystic fibrosis. Pediatrics 1996;97:524-8.
13. Padoan R, Bassotti A, Seia M, Corbetta C. Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations. Eur J Pediatr 2002;161:212-5.
14. Ruddy RM, Scanlin TF. Abnormal sweat electrolytes in a case of celiac disease and a case of psychosocial failure to thrive. Review of other reported causes. Clin Pediatr 1987; 26(2):83-9.
15. Stern RC. The Diagnosis of Cystic Fibrosis. NEJM 1997;336(7):487-91.
16. Nelson. Textbook of Pediatrics, 17th edition, pg. 1441-2.
17. Southern KW, Noone PG, Bosworth DG, LeGrys VA, Knowles MR, Barker PM. A modified technique for measurement of nasal transepithelial potential difference in infants. J Pediatr 2001;139:353-8.
18. Le Grys VA, Wood RE. Incidence and implications of false-negative sweat test reports in patients with cystic fibrosis. Pediatr Pulmonol 1988;4(3):169-72.
19. Desmarquest P, Feldmann D, Tamalat A, Boule M, Faurox B, Tournier G, et al. Genotype Analysis and Phenotypic Manifestations of Children with Intermediate Sweat Chloride Test Result. Chest 2000;118:1591-7.
20. Lebecque P, Leal T, De Boeck C, Jaspers M, Cuppens H, Cassiman JJ. Mutations of the Cystic Fibrosis Gene and Intermediate Sweat Chloride Levels in Children. Am J Resp Crit Care Med 2002;165:757-61.
21. Augarten A, Berman H, Aviram M, Diver- Habber A, Akons H, Ben TL, et al. Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests. Clin Exp Med 2003;3 (2):119-23.
2. NCCLS. Sweat testing: Sample collection and Quantitative Analysis: Approved Guideline- Second Edition. NCCLS document C34-A2 [ISBN 1-56238-407-4]. NCCLS, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania USA, 2000.
3. Baumer JH. “Evidence based guidelines for the performance of sweat test for the investigation of cystic fibrosis in UK. Arch Dis Child 2003;88:1126-7.
4. Rosenstein BJ, et al. “The diagnosis of cystic fibrosis: a Consensus Statement. J Pediatr 1998;132(4):589-95.
5. Cystic Fibrosis Foundation. The diagnosis of Cystic Fibrosis. Consensus Statement. Consensus Conference, 1996, VII: sect.1.
6. Rosenstein BJ, Zeitlin PL. Cystic fibrosis. Lancet 1998;351:277-82.
7. Mastella G. Fibrosi cistica. Da: Argomenti di Malattie respiratorie infantili. Pisa, Pacini editore, 1998:95-142.
8. Salvatore D, Marchetti F, D’Andrea N, Schiavo MV. La fibrosi cistica in Basilicata: aspetti epidemiologici, clinici ed assistenziali. Bollettino OER 2001;vol. 1:12-15.
9. Vazquez C, Azcarate MJ, Sojo A, et al. Results of the sweat test, carried out by 2 methods, for the diagnosis of cystic fibrosis. An Esp Pediatr 1987;26(1):33-6.
10. Webster HL. Laboratory diagnosis of cystic fibrosis. Crit Rev Clin Lab Sci 1983;18(4): 313-38.
11. Rosenstein BJ. What is a cystic fibrosis diagnosis? Clin Chest Med 1998;19(3):423-41.
12. Farrell PM, Koscik RE. Sweat chloride concentrations in infants homozygous or heterozygous for DF508 cystic fibrosis. Pediatrics 1996;97:524-8.
13. Padoan R, Bassotti A, Seia M, Corbetta C. Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations. Eur J Pediatr 2002;161:212-5.
14. Ruddy RM, Scanlin TF. Abnormal sweat electrolytes in a case of celiac disease and a case of psychosocial failure to thrive. Review of other reported causes. Clin Pediatr 1987; 26(2):83-9.
15. Stern RC. The Diagnosis of Cystic Fibrosis. NEJM 1997;336(7):487-91.
16. Nelson. Textbook of Pediatrics, 17th edition, pg. 1441-2.
17. Southern KW, Noone PG, Bosworth DG, LeGrys VA, Knowles MR, Barker PM. A modified technique for measurement of nasal transepithelial potential difference in infants. J Pediatr 2001;139:353-8.
18. Le Grys VA, Wood RE. Incidence and implications of false-negative sweat test reports in patients with cystic fibrosis. Pediatr Pulmonol 1988;4(3):169-72.
19. Desmarquest P, Feldmann D, Tamalat A, Boule M, Faurox B, Tournier G, et al. Genotype Analysis and Phenotypic Manifestations of Children with Intermediate Sweat Chloride Test Result. Chest 2000;118:1591-7.
20. Lebecque P, Leal T, De Boeck C, Jaspers M, Cuppens H, Cassiman JJ. Mutations of the Cystic Fibrosis Gene and Intermediate Sweat Chloride Levels in Children. Am J Resp Crit Care Med 2002;165:757-61.
21. Augarten A, Berman H, Aviram M, Diver- Habber A, Akons H, Ben TL, et al. Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests. Clin Exp Med 2003;3 (2):119-23.