Peadar G. Noone
Division of Pulmonary and Critical Care Medicine
Pulmonary/Cystic Fibrosis Research and Treatment Center
University of North Carolina at Chapel Hill
Chapel Hill
USA
Name/email consistency: high
- Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia. Noone, P.G., Zariwala, M., Sannuti, A., Minnix, S., Leigh, M.W., Carson, J., Knowles, M.R. Chest (2002)
- Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center study. Noone, P.G., Hamblett, N., Accurso, F., Aitken, M.L., Boyle, M., Dovey, M., Gibson, R., Johnson, C., Kellerman, D., Konstan, M.W., Milgram, L., Mundahl, J., Retsch-Bogort, G., Rodman, D., Williams-Warren, J., Wilmott, R.W., Zeitlin, P., Ramsey, B. Pediatr. Pulmonol. (2001)
- 'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations. Noone, P.G., Knowles, M.R. Respir. Res. (2001)
- Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosis. Noone, P.G., Hohneker, K.W., Zhou, Z., Johnson, L.G., Foy, C., Gipson, C., Jones, K., Noah, T.L., Leigh, M.W., Schwartzbach, C., Efthimiou, J., Pearlman, R., Boucher, R.C., Knowles, M.R. Mol. Ther. (2000)
- Discordant organ laterality in monozygotic twins with primary ciliary dyskinesia. Noone, P.G., Bali, D., Carson, J.L., Sannuti, A., Gipson, C.L., Ostrowski, L.E., Bromberg, P.A., Boucher, R.C., Knowles, M.R. Am. J. Med. Genet. (1999)
- Airway deposition and clearance and systemic pharmacokinetics of amiloride following aerosolization with an ultrasonic nebulizer to normal airways. Noone, P.G., Regnis, J.A., Liu, X., Brouwer, K.L., Robinson, M., Edwards, L., Knowles, M.R. Chest (1997)