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Michael Knowles
Michael Knowles
Professor of Medicine, Univ of North Carolina
Verified email at med.unc.edu
Title
Cited by
Cited by
Year
Mucus clearance as a primary innate defense mechanism for mammalian airways
MR Knowles, RC Boucher
The Journal of clinical investigation 109 (5), 571-577, 2002
16342002
Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis
JA Cohn, KJ Friedman, PG Noone, MR Knowles, LM Silverman, ...
New England Journal of Medicine 339 (10), 653-658, 1998
11451998
Primary ciliary dyskinesia: diagnostic and phenotypic features
PG Noone, MW Leigh, A Sannuti, SL Minnix, JL Carson, M Hazucha, ...
American journal of respiratory and critical care medicine 169 (4), 459-467, 2004
8952004
Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice
C Castellani, H Cuppens, M Macek Jr, JJ Cassiman, E Kerem, P Durie, ...
Journal of cystic fibrosis 7 (3), 179-196, 2008
8642008
Mucus clearance and lung function in cystic fibrosis with hypertonic saline
SH Donaldson, WD Bennett, KL Zeman, MR Knowles, R Tarran, ...
New England Journal of Medicine 354 (3), 241-250, 2006
8452006
Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis
M Knowles, J Gatzy, R Boucher
New England Journal of Medicine 305 (25), 1489-1495, 1981
7621981
Nontuberculous mycobacteria: I: multicenter prevalence study in cystic fibrosis
KN Olivier, DJ Weber, RJ Wallace Jr, AR Faiz, JH Lee, Y Zhang, ...
American journal of respiratory and critical care medicine 167 (6), 828-834, 2003
7402003
A controlled study of adenoviral-vector–mediated gene transfer in the nasal epithelium of patients with cystic fibrosis
MR Knowles, KW Hohneker, Z Zhou, JC Olsen, TL Noah, PC Hu, ...
New England Journal of Medicine 333 (13), 823-831, 1995
7141995
Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation.
RC Boucher, MJ Stutts, MR Knowles, L Cantley, JT Gatzy
The Journal of clinical investigation 78 (5), 1245-1252, 1986
7011986
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry
H Olbrich, K Häffner, A Kispert, A Völkel, A Volz, G Sasmaz, R Reinhardt, ...
Nature genetics 30 (2), 143-144, 2002
6482002
Abnormal ion permeation through cystic fibrosis respiratory epithelium
MR Knowles, MJ Stutts, A Spock, N Fischer, JT Gatzy, RC Boucher
Science 221 (4615), 1067-1070, 1983
6291983
Genetic modifiers of lung disease in cystic fibrosis
ML Drumm, MW Konstan, MD Schluchter, A Handler, R Pace, F Zou, ...
New England Journal of Medicine 353 (14), 1443-1453, 2005
6082005
Activation by extracellular nucleotides of chloride secretion in the airway epithelia of patients with cystic fibrosis
MR Knowles, LL Clarke, RC Boucher
New England Journal of Medicine 325 (8), 533-538, 1991
5981991
Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease
MR Knowles, LA Daniels, SD Davis, MA Zariwala, MW Leigh
American journal of respiratory and critical care medicine 188 (8), 913-922, 2013
5612013
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome
MW Leigh, JE Pittman, JL Carson, TW Ferkol, SD Dell, SD Davis, ...
Genetics in Medicine 11 (7), 473-487, 2009
5552009
A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations
WE Highsmith, LH Burch, Z Zhou, JC Olsen, TE Boat, A Spock, JD Gorvoy, ...
New England Journal of Medicine 331 (15), 974-980, 1994
5201994
Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia
MP Kennedy, H Omran, MW Leigh, S Dell, L Morgan, PL Molina, ...
Circulation 115 (22), 2814-2821, 2007
4962007
Recommendations for the classification of diseases as CFTR-related disorders
C Bombieri, M Claustres, K De Boeck, N Derichs, J Dodge, E Girodon, ...
Journal of Cystic Fibrosis 10, S86-S102, 2011
4762011
Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis
M Corey, L Edwards, H Levison, M Knowles
The Journal of pediatrics 131 (6), 809-814, 1997
4411997
A pilot study of aerosolized amiloride for the treatment of lung disease in cystic fibrosis
MR Knowles, NL Church, WE Waltner, JR Yankaskas, P Gilligan, M King, ...
New England Journal of Medicine 322 (17), 1189-1194, 1990
3971990
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