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The New England Journal of Medicine|July 15, 1999
Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronismE Kerem, T Bistritzer, A Hanukoglu, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
Mechanism of inositol monophosphatase, the putative target of lithium therapyS J Pollack, J R Atack, M R Knowles, et al.
American Journal of Medical Genetics|February 6, 1999
Discordant organ laterality in monozygotic twins with primary ciliary dyskinesiaP G Noone, D Bali, J L Carson, et al.
American Journal of Respiratory and Critical Care Medicine|November 9, 2000
Lung disease associated with the IVS8 5T allele of the CFTR geneP G Noone, C A Pue, Z Zhou, et al.
The New England Journal of Medicine|April 26, 1990
A pilot study of aerosolized amiloride for the treatment of lung disease in cystic fibrosisM R Knowles, N L Church, W E Waltner, et al.
American Journal of Human Genetics|May 1, 1997
Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%M Macek, A Mackova, A Hamosh, et al.
Pharmacotherapy|March 1, 1997
Pharmacokinetics of amiloride after inhalation and oral administration in adolescents and adults with cystic fibrosisK M Jones, E Liao, K Hohneker, et al.
American Journal of Respiratory and Critical Care Medicine|October 1, 1995
Screening Young syndrome patients for CFTR mutationsK J Friedman, H Teichtahl, D M De Kretser, et al.
Clinical Chemistry|October 1, 1990
Frequency of the delta Phe508 mutation and correlation with XV.2c/KM-19 haplotypes in an American population of cystic fibrosis patients: results of a collaborative studyW E Highsmith, G L Chong, H T Orr, et al.
Biochemistry|August 16, 1994
Structural analysis of inositol monophosphatase complexes with substratesR Bone, L Frank, J P Springer, et al.
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