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References
25
[1]
Hamosh A, Fitz Simmons SC, Macek M, Knowles MR, Rosenstein BJ, Cutting GR. Comparison for the clinical manifestations of cystic fibrosis in the Blacks and the Whites.J Pediatr 1998; 132: 255–257. 10.1016/s0022-3476(98)70441-x
[2]
Cystic fibrosis-an Indian perspective on recent advances in diagnosis and management

S. K. Kabra, Madhulika Kabra, M. Ghosh et al.

The Indian Journal of Pediatrics 1996 10.1007/bf02845243
[3]
Kabra M, Ghosh M, Kabra SK, Khanna A, Verma IC. AF 508 mutations in Indian children with cystic fibrosis.Indian J Med Res 1996; 104: 355–358.
[4]
Powers CA, Potter EM, Wessel HU, Kloyd-Still JD. Cystic fibrosis in Asian Indians.Arch Pediatr Adoles Med 1996; 150: 554–555. 10.1001/archpedi.1996.02170300108024
[5]
Spencer DA, Venkatraman M, Steversam HK, Weller PH. Cystic fibrosis in children from ethnic minorities in the west midlands.Respir Medicine 1994; 88: 671–675. 10.1016/s0954-6111(05)80065-4
[6]
Goodchilds MC, Insley J, Rushton DI, Gaze H. Cystic fibrosis in 3 Pakistani children.Arch Dis Child 1974; 49:739–741. 10.1136/adc.49.9.739
[7]
Bowlers IM, Estelin EJ, Littlewood JM. Cystic fibrosis in Asians.Arch Dis Child 1993; 68:120–122. 10.1136/adc.68.1.120
[8]
Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: consensus statement.J Pediatr 1998; 132:589–595. 10.1016/s0022-3476(98)70344-0
[9]
Stern RC, Boat TF, Doershuk CF. Obstructive azoospermia as a diagnostic criteria to cystic fibrosis syndrome.Lancet 1982; 198:589–595.
[10]
Wallis C. Diagnosing cystic fibrosis: Blood, sweat and tears.Arch Dis Child 1997; 96:85–91. 10.1136/adc.76.2.85
[11]
Le Grys VA. Sweat testing for diagnosis of cystic fibrosis: Practical considerations.J Pediatr 1996; 129 : 892–897. 10.1016/s0022-3476(96)70034-3
[12]
Khanna A. A pilot study for clinical features and frequency of AF 508 mutation in Indian children with cystic fibrosis. Thesis submitted to Faculty of AIIMS for MD 1997.
[13]
Super M. Can manifesting heterozygote have cystic fibrosis?Thorax 1999; 54:194–195. 10.1136/thx.54.3.194
[14]
Hanmond KB, Turcobs NL, Gibson LE. Clinical evaluation of the macroduct sweat collection system and conductivity analysis in the diagnosis of cystic fibrosis.J Pediatr 1994; 124: 255–68. 10.1016/s0022-3476(94)70314-0
[15]
Disant Agnese PA, Darling RC, Ferera GA, Shea E. Abnormal electrolytes composition of sweat in cystic fibrosis of pancreas: Clinical significance and relationship to disease.Pediatrics 1953; 12 : 549–563. 10.1542/peds.12.5.549
[16]
Kerem B, Rommens JN, Bichnan JAet al. Identification of the cystic fibrosis gene: Genetic analysis.Science 1989; 245 : 1673–1680. 10.1126/science.2570460
[17]
Stern RC. Current concepts in the diagnosis of cystic fibrosis.N Eng J Med 1997; 336:487–491. 10.1056/nejm199702133360707
[18]
Wilmott RW. Making the diagnosis of cystic fibrosis.J Pediatr 1998; 132: 563–565. 10.1016/s0022-3476(98)70337-3
[19]
Wilson DC, Ellis L, Zielenski Jet al. Uncertainty in the diagnosis of cystic fibrosis: Possible role ofin vivo nasal potential difference measurements.J Pediatr 1998; 132:596–599. 10.1016/s0022-3476(98)70345-2
[20]
Knowles MR, Gatzy J, Boucher R. Relative ion permeability of normal and cystic fibrosis nasal epithelium.J Clin Invest 1983; 71:1410–1418. 10.1172/jci110894
[21]
Thomssen MJ, Demco CA, Doershuk CF. Cystic fibrosis: a review of pulmonary infections and interventions.Pediatr Pulmonol 1987; 3: 334–351. 10.1002/ppul.1950030510
[22]
Fitz Simmons SC. The changing epidemiology of cystic fibrosis.J Pediatr 1993; 122:l-9.
[23]
Couper R. Pancreatic function test. In: Walker WA, Durie PR, Hamilton JR, Walker-Smith JG (eds).pediatric Gastrointestinal Disease : Pathophysiology, Diagnosis, Management. 2nd edn. St. Louise Mosby, 1995; 1621–1634.
[24]
Wallis C, Leung TH, Cubbit D, Reynolds A. Stool elastase as a diagnostic test for pancreatic function in children with cystic fibrosis.Lancet 1997; 350:1001. 10.1016/s0140-6736(97)24040-7
[25]
Fairhurst JJ. Imaging. In: Hill CM and Dodge JA (eds).Practical Guidelines for Cystic Fibrosis Care. London, Churchill Livingstone 1998; 159–170.
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References
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Published
Nov 01, 1999
Vol/Issue
66(6)
Pages
923-928
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Cite This Article
S. K. Kabra, Madhulika, G. J. Connett, et al. (1999). Diagnosis of cystic fibrosis : Indian perspective. The Indian Journal of Pediatrics, 66(6), 923-928. https://doi.org/10.1007/bf02723869
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