-
1
-
-
0026667894
-
Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains
-
ANDERSON M.P., WELSH M.J. (1992). Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains. Science. 257, 1701-1704.
-
(1992)
Science.
, vol.257
, pp. 1701-1704
-
-
Anderson, M.P.1
Welsh, M.J.2
-
2
-
-
0030768159
-
Lower airway inflammation in infants and young children with cystic fibrosis
-
ARMSTRONG D.S., GRIMWOOD K., CARLIN J.B., CARZINO R., GUTIERREZ J.P., HULL J., OLINSKY A., PHELAN E.M., ROBERTSON C.F., PHELAN P.D. (1997). Lower airway inflammation in infants and young children with cystic fibrosis. Am. J. Respir. Crit. Care Med. 156, 1197-1204. (Pubitemid 27446528)
-
(1997)
American Journal of Respiratory and Critical Care Medicine
, vol.156
, Issue.4
, pp. 1197-1204
-
-
Armstrong, D.S.1
Grimwood, K.2
Carlin, J.B.3
Carzino, R.4
Gutierrez, J.P.5
Hull, J.6
Olinsky, A.7
Phelan, E.M.8
Robertson, C.F.9
Phelan, P.D.10
-
3
-
-
0037288208
-
Prevalence of Aspergillus fumigatus and other fungal species in the sputum of adult patients with cystic fibrosis
-
BAKARE N., RICKERTS Y., BARGON J., JUST-NUBLING G. (2003). Prevalence of Aspergillus fumigatus and other fungal species in the sputum of adult patients with cystic fibrosis. Mycoses. 46, 19-23.
-
(2003)
Mycoses
, vol.46
, pp. 19-23
-
-
Bakare, N.1
Rickerts, Y.2
Bargon, J.3
Just-Nubling, G.4
-
4
-
-
51449098793
-
Molecular detection of multiple emerging pathogens in sputa from cystic fibrosis patients
-
BITTAR F., RICHET H., DUBUS J.C., REYNAUD-GAUBERT M., STREMLER N., SARLES J., RAOULT D., ROLAIN J.M. (2008). Molecular detection of multiple emerging pathogens in sputa from cystic fibrosis patients. PloSONE. 3, 2908.
-
(2008)
PloSONE.
, vol.3
, pp. 2908
-
-
Bittar, F.1
Richet, H.2
Dubus, J.C.3
Reynaud-Gaubert, M.4
Stremler, N.5
Sarles, J.6
Raoult, D.7
Rolain, J.M.8
-
5
-
-
0037027912
-
An overview of the pathogenesis of cystic fibrosis lung disease
-
DOI 10.1016/S0169-409X(02)00144-8, PII S0169409X02001448
-
BOUCHER R.C. (2002). An overview of the pathogenesis of cystic fibrosis lung disease. Adv. Drug Deliv. Rev. 54, 1359-1371. (Pubitemid 35375765)
-
(2002)
Advanced Drug Delivery Reviews
, vol.54
, Issue.11
, pp. 1359-1371
-
-
Boucher, R.C.1
-
6
-
-
0020672729
-
Transtracheal aspiration in pulmonary infection in children with cystic fibrosis
-
BROOK I., FINK R. (1983). Transtracheal aspiration in pulmonary infection in children with cystic fibrosis. Eur. J. Respir. Dis. 64, 51-57.
-
(1983)
Eur. J. Respir. Dis.
, vol.64
, pp. 51-57
-
-
Brook, I.1
Fink, R.2
-
7
-
-
0031874764
-
Microbiology of sputum from patients at cystic fibrosis centers in the UNited States
-
BURNS J.L., EMERSON J., STAPP J.R., YIM D.L., KRZEWINSKI J., LOUDEN L., RAMSEY B.W., CLAUSEN C.R. (1998). Microbiology of sputum from patients at cystic fibrosis centers in the United States. Clin. Infect. Dis. 27, 158-163. (Pubitemid 28334435)
-
(1998)
Clinical Infectious Diseases
, vol.27
, Issue.1
, pp. 158-163
-
-
Burns, J.L.1
Emerson, J.2
Stapp, J.R.3
Yim, D.L.4
Krzewinski, J.5
Louden, L.6
Ramsey, B.W.7
Clausen, C.R.8
-
8
-
-
0032867016
-
Chronic airway colonization by Penicillium emersonii in a patient with cystic fibrosis
-
DOI 10.1046/j.1365-280X.1999.00232.x
-
CIMON B., CARRERE J., CHAZALETTE J.P., VINATIER J.F., CHABASSE D., BOUCHARA J.P. (1999). Chronic airway colonization by Penicillium emersonii in a patient with Cystic Fibrosis. Med. Mycol. 37, 291-293. (Pubitemid 29364146)
-
(1999)
Medical Mycology
, vol.37
, Issue.4
, pp. 291-293
-
-
Cimon, B.1
Carrere, J.2
Chazalette, J.P.3
Vinatier, J.F.4
Chabasse, D.5
Bouchara, J.P.6
-
9
-
-
0033952695
-
Clinical significance of Scedosporium apiospermum in patients with cystic fibrosis
-
CIMON B., CARRERE J., VINATIER J.F., CHAZALETTE J.P., CHABASSE D., BOUCHARA J.P. (2000). Clinical significance of Scedosporium apiospermum in patients with cystic fibrosis. Eur. J. Clin. Microbiol. Infect. Dis. 19, 53-56.
-
(2000)
Eur. J. Clin. Microbiol. Infect. Dis.
, vol.19
, pp. 53-56
-
-
Cimon, B.1
Carrere, J.2
Vinatier, J.F.3
Chazalette, J.P.4
Chabasse, D.5
Bouchara, J.P.6
-
11
-
-
0036265949
-
Characterization of unusual bacteria isolated from respiratory secretions of cystic fibrosis patients and description of Inquilinus limosus gen. nov., sp. nov
-
COENYE T., GORIS J., SPILKER T., VANDAMME P., LIPUMA J.J. (2002). Characterization of unusual bacteria isolated from respiratory secretions of cystic fibrosis patients and description of Inquilinus limosus gen. nov., sp. nov. J. Clin. Microbiol. 40, 2062-2069.
-
(2002)
J. Clin. Microbiol.
, vol.40
, pp. 2062-2069
-
-
Coenye, T.1
Goris, J.2
Spilker, T.3
Vandamme, P.4
Lipuma, J.J.5
-
12
-
-
0036529046
-
Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis
-
DAKIN C.J., NUMA A.H., WANG H., MORTON J.R., VERTZYAS CC, HENRY R.L. (2002). Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis. Am. J. Respir. Crit. Care Med. 165, 904-910. (Pubitemid 34774655)
-
(2002)
American Journal of Respiratory and Critical Care Medicine
, vol.165
, Issue.7
, pp. 904-910
-
-
Dakin, C.J.1
Numa, A.H.2
Wang, H.3
Morton, J.R.4
Vertzyas, C.C.5
Henry, R.L.6
-
13
-
-
0036259779
-
Genotyping study of Scedosporium apiospermum isolates with cystic fibrosis
-
DEFONTAINE A., ZOUHAIR R., CIMON B., CARRERE J., BAILLY E., SYMOENS F., DIOURI M., HALLET J.N., BOUCHARA J.P. (2002). Genotyping study of Scedosporium apiospermum isolates with cystic fibrosis. J. Clin. Microbiol. 40, 2108-2114.
-
(2002)
J. Clin. Microbiol.
, vol.40
, pp. 2108-2114
-
-
Defontaine, A.1
Zouhair, R.2
Cimon, B.3
Carrere, J.4
Bailly, E.5
Symoens, F.6
Diouri, M.7
Hallet, J.N.8
Bouchara, J.P.9
-
14
-
-
0026781952
-
Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive
-
DENNING G.M., ANDERSON M.P., AMARA J.F., MARSHALL J., SMITH A.E., WELSH M.J. (1992). Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive. Nature. 358, 761-764.
-
(1992)
Nature
, vol.358
, pp. 761-764
-
-
Denning, G.M.1
Anderson, M.P.2
Amara, J.F.3
Marshall, J.4
Smith, A.E.5
Welsh, M.J.6
-
15
-
-
0018817749
-
A scheme for the identification of clinical isolates of gram-negative anaerobic bacilli by conventional bacteriological tests
-
DUERDEN B.I., COLEE J.G., BROWN R., DEACON A.G., HOLBROOK W.P. (1980). A scheme for the identification of clinical isolates of gram-negative anaerobic bacilli by conventional bacteriological tests. J. Med. Microbiol. 13, 231-245.
-
(1980)
J. Med. Microbiol.
, vol.13
, pp. 231-245
-
-
Duerden, B.I.1
Colee, J.G.2
Brown, R.3
Deacon, A.G.4
Holbrook, W.P.5
-
16
-
-
0020469219
-
Recent experience with antimicrobial susceptibility of anaerobic bacteria. Increasing resistance to penicillin
-
EDSON R.S., RESENBLATT J.E., LEE D.T., MCVEY E.A. (1982). Recent experience with antimicrobial susceptibility of anaerobic bacteria; increasing resistance to penicillin. Mayo Clin. Proc. 57, 737-741. (Pubitemid 13221587)
-
(1982)
Mayo Clinic Proceedings
, vol.57
, Issue.12
, pp. 737-741
-
-
Edson, R.S.1
Rosenblatt, J.E.2
Lee, D.T.3
McVey III, E.A.4
-
17
-
-
0036683366
-
Detecting Stenotrophomonas maltophilia does not reduce survival of patients with cystic fibrosis
-
Goss C.H., OTTO K., AITKEN M.L., RUBENFELD G.D. (2002). Detecting Stenotrophomonas maltophilia does not reduce survival of patients with cystic fibrosis. Am. J. Respir. Crit. Care. Med. 166, 356-361.
-
(2002)
Am. J. Respir. Crit. Care. Med.
, vol.166
, pp. 356-361
-
-
Goss, C.H.1
Otto, K.2
Aitken, M.L.3
Rubenfeld, G.D.4
-
19
-
-
38049129070
-
Molecular identification of bacteria in bronchoalveolar lavage fluid from children with cystic fibrosis
-
HARRIS JK, DE GROOTE MA, SAGEL SD, ZEMANICK ET, KAPSNER R, PENVARI C, KAESS H, DETERDING R.R., ACCURSO F.J., PACE N.R. (2007). Molecular identification of bacteria in bronchoalveolar lavage fluid from children with cystic fibrosis. Proc. Natl. Acad. Sci. USA. 104, 20529-20533.
-
(2007)
Proc. Natl. Acad. Sci. USA.
, vol.104
, pp. 20529-20533
-
-
Harris, J.K.1
De Groote, M.A.2
Sagel, S.D.3
Zemanick, E.T.4
Kapsner, R.5
Penvari, C.6
Kaess, H.7
Deterding, R.R.8
Accurso, F.J.9
Pace, N.R.10
-
20
-
-
0034878704
-
Alginate overproduction affects Pseudomonas aeruginosa biofilm structure and function
-
HENTZER M., TEITZEL G.M., BALZER G.J., HEYDORN A., MOLIN S., GIvsKov M., PARSEK M.R. (2001). Alginate overproduction affects Pseudomonas aeruginosa biofilm structure and function. J. Bacteriol. 183, 5395-5401.
-
(2001)
J. Bacteriol.
, vol.183
, pp. 5395-5401
-
-
Hentzer, M.1
Teitzel, G.M.2
Balzer, G.J.3
Heydorn, A.4
Molin, S.5
Givskov, M.6
Parsek, M.R.7
-
21
-
-
26944461986
-
Antibiotic susceptabilities of Pseudomonas aeruginosa isolates derived from patients with cystic fibrosis under aerobic, anaerobic, and biofilm conditions
-
HILL D., ROSE B., PAJKOS A., ROBINSON M., BYE P., BELL S., ELKINS M., THOMPSON B., MACLEOD C., AARON S.D., HARBOUR C. (2005). Antibiotic susceptabilities of Pseudomonas aeruginosa isolates derived from patients with cystic fibrosis under aerobic, anaerobic, and biofilm conditions. J. Clin. Microbiol. 43, 5085-5090.
-
(2005)
J. Clin. Microbiol.
, vol.43
, pp. 5085-5090
-
-
Hill, D.1
Rose, B.2
Pajkos, A.3
Robinson, M.4
Bye, P.5
Bell, S.6
Elkins, M.7
Thompson, B.8
Macleod, C.9
Aaron, S.D.10
Harbour, C.11
-
22
-
-
0025359917
-
The incidence of anaerobes in the sputum of patients with cystic fibrosis
-
JEWES L.A., SPENCER R.C. (1990). The incidence of anaerobes in the sputum of patients with cystic fibrosis. J. Med. Microbiol. 31, 271-274. (Pubitemid 20124013)
-
(1990)
Journal of Medical Microbiology
, vol.31
, Issue.4
, pp. 271-274
-
-
Jewes, L.A.1
Spencer, R.C.2
-
23
-
-
0036194724
-
Mucus clearance as a primary innate defense mechanism for mammalian airways
-
KNOWLES M.R., BOUCHER R.C. (2002). Mucus clearance as a primary innate defense mechanism for mammalian airways. J. Clin. Invest. 109, 571-577.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 571-577
-
-
Knowles, M.R.1
Boucher, R.C.2
-
24
-
-
32044445488
-
Microbiology of airway disease in a cohort of patients with cystic fibrosis
-
LAMBIASE A., RAIA V., DEL PEZZO M., SEPE A., CARNOVALE V., ROSSANO F. (2006). Microbiology of airway disease in a cohort of patients with cystic fibrosis BMC. Infect. Dis. 6, 4.
-
(2006)
BMC. Infect. Dis.
, vol.6
, pp. 4
-
-
Lambiase, A.1
Raia, V.2
Del Pezzo, M.3
Sepe, A.4
Carnovale, V.5
Rossano, F.6
-
25
-
-
36049051982
-
Chryseobacterium respiratory tract infections in patients with cystic fibrosis
-
DOI 10.1016/j.jinf.2007.08.002, PII S0163445307007311
-
LAMBIASE A., DEL PEZZO M., RAIA V., SEPE A., FERRI P., ROSSANO F. (2007). Chryseobacterium respiratory tract infections in patients with cystic fibrosis. J. Infect. 55, 518-523. (Pubitemid 350082468)
-
(2007)
Journal of Infection
, vol.55
, Issue.6
, pp. 518-523
-
-
Lambiase, A.1
Del Pezzo, M.2
Raia, V.3
Sepe, A.4
Ferri, P.5
Rossano, F.6
-
26
-
-
77049113297
-
Sphingobacterium respiratory tract infection in patients with cystic fibrosis
-
LAMBIASE A., ROSSANO F., DEL PEZZO M., RAIA V., SEPE A., DE GREGORIO F., CATANIA M.R. (2009). Sphingobacterium respiratory tract infection in patients with cystic fibrosis. BMC. Res. Notes. 2, 262.
-
(2009)
BMC. Res. Notes.
, vol.2
, pp. 262
-
-
Lambiase, A.1
Rossano, F.2
Del Pezzo, M.3
Raia, V.4
Sepe, A.5
De Gregorio, F.6
Catania, M.R.7
-
27
-
-
0036225688
-
Lung infections associated with cystic fibrosis
-
DOI 10.1128/CMR.15.2.194-222.2002
-
LYCZAK J.B., CANNON C.L., PIER G.B. (2002). Lung infections associated with cystic fibrosis. Clin. Microbiol. Rev. 15, 194-222. (Pubitemid 34303763)
-
(2002)
Clinical Microbiology Reviews
, vol.15
, Issue.2
, pp. 194-222
-
-
Lyczak, J.B.1
Cannon, C.L.2
Pier, G.B.3
-
28
-
-
0032433707
-
Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airway disease
-
MATSUI H., GRUBB B.R., TARRAN R., RANDELL S.H., GATZY J.T., DAVIS C.W., BOUCHER R.C. (1998). Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airway disease. Cell. 95, 1005-1015.
-
(1998)
Cell.
, vol.95
, pp. 1005-1015
-
-
Matsui, H.1
Grubb, B.R.2
Tarran, R.3
Randell, S.H.4
Gatzy, J.T.5
Davis, C.W.6
Boucher, R.C.7
-
29
-
-
33746625956
-
The place of molecular genetic methods in the diagnostics of human pathogenic anaerobic bacteria
-
NAGY E., URBAN E., SOKI J., TERHES G., NAGY K. (2006). The place of molecular genetic methods in the diagnostics of human pathogenic anaerobic bacteria. Acta Microbiol. Immunol. Hung. 53, 183-194.
-
(2006)
Acta Microbiol. Immunol. Hung.
, vol.53
, pp. 183-194
-
-
Nagy, E.1
Urban, E.2
Soki, J.3
Terhes, G.4
Nagy, K.5
-
30
-
-
0022618961
-
Occurrence of clindamycin-resistant anaerobic bacteria isolated from cultures taken following clindamycin therapy
-
OHM-SMITH M.J., SWEET R.L., HADLEY W.K. (1986). Occurrence of clindamycin-resistant anaerobic bacteria isolated from cultures taken following clindamycin therapy. Antimicrob. Agents Chemoter. 30, 11-14.
-
(1986)
Antimicrob. Agents Chemoter.
, vol.30
, pp. 11-14
-
-
Ohm-Smith, M.J.1
Sweet, R.L.2
Hadley, W.K.3
-
31
-
-
0037445208
-
Nontuberculous mycobacteria. II: Nested cohort study of impact on cystic fibrosis lung disease
-
NONTUBERCULOUS MYCOBACTERIA IN CYSTIC FIBROSIS STUDY GROUP
-
OLIVIER K.N., WEBER D.J., LEE J.H., HANDLER A., TUDOR G., MOLINA P.L., TOMASHEFSKI J., KNOWLES M.R.; NONTUBERCULOUS MYCOBACTERIA IN CYSTIC FIBROSIS STUDY GROUP. (2003). Nontuberculous mycobacteria. II: nested cohort study of impact on cystic fibrosis lung disease. Am. J. Respir. Crit. Care Med. 167, 835-840.
-
(2003)
Am. J. Respir. Crit. Care Med.
, vol.167
, pp. 835-840
-
-
Olivier, K.N.1
Weber, D.J.2
Lee, J.H.3
Handler, A.4
Tudor, G.5
Molina, P.L.6
Tomashefski, J.7
Knowles, M.R.8
-
32
-
-
34250328344
-
Membrane-bound nitrate reductase is required for anaerobic growth in cystic fibrosis sputum
-
PALMER K.L., BROWN S.A., WHITELEY M. (2007). Membrane-bound nitrate reductase is required for anaerobic growth in cystic fibrosis sputum. J. Bacteriol. 189, 4449-4455.
-
(2007)
J. Bacteriol.
, vol.189
, pp. 4449-4455
-
-
Palmer, K.L.1
Brown, S.A.2
Whiteley, M.3
-
33
-
-
0029177535
-
Effects of Pseudomonas aeruginosa colonization on lung function and anthropometric variables in children with cystic fibrosis
-
PAMUKCU A., BUSH A., BUCHDAHL R. (1995) Effects of Pseudomonas aeruginosa colonization on lung function and anthropometric variables in children with cystic fibrosis. Pediatr. Pulmunol. 19, 10-15.
-
(1995)
Pediatr. Pulmunol.
, vol.19
, pp. 10-15
-
-
Pamukcu, A.1
Bush, A.2
Buchdahl, R.3
-
34
-
-
0025156799
-
Anaerobic bacteria and bacterial infections: Perspectives on treatment and resi stance in Italy
-
PANICHI G., DI ROSA R., ENRICO P., BABUDIERI S. (1990). Anaerobic bacteria and bacterial infections: perspectives on treatment and resi stance in Italy. Rev. Infect. Dis. 12, 152-156.
-
(1990)
Rev. Infect. Dis.
, vol.12
, pp. 152-156
-
-
Panichi, G.1
Di Rosa, R.2
Enrico, P.3
Babudieri, S.4
-
35
-
-
0030021470
-
Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections
-
PIER G.B., GROUT M., ZAIDI T.S., OLSEN J.C., JOHNSON L.G., YANKASKAS J.R., GOLDBERG J.B. (1996). Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections. Science. 271, 64-67.
-
(1996)
Science.
, vol.271
, pp. 64-67
-
-
Pier, G.B.1
Grout, M.2
Zaidi, T.S.3
Olsen, J.C.4
Johnson, L.G.5
Yankaskas, J.R.6
Goldberg, J.B.7
-
36
-
-
67449104896
-
Occurrence and relevance of filamentous fungi in respiratory secretions of patients with cystic fibrosis - A review
-
PIHET M., CARRERE J., CIMON B., CHABASSE D., DELHAES L., SYMOENS F., BOUCHARA J.P. (2009). Occurrence and relevance of filamentous fungi in respiratory secretions of patients with cystic fibrosis-a review. Med. Mycol. 47, 387-397.
-
(2009)
Med. Mycol.
, vol.47
, pp. 387-397
-
-
Pihet, M.1
Carrere, J.2
Cimon, B.3
Chabasse, D.4
Delhaes, L.5
Symoens, F.6
Bouchara, J.P.7
-
37
-
-
0036125965
-
Pulmonary infections in patients with cystic fibrosis
-
DOI 10.1053/srin.2002.31690
-
RAJAN S., SAIMAN L. (2002). Pulmonary infections in patients with cystic fibrosis. Semin. Respir. Infect. 17, 47-56. (Pubitemid 34233391)
-
(2002)
Seminars in Respiratory Infections
, vol.17
, Issue.1
, pp. 47-56
-
-
Rajan, S.1
Saiman, L.2
-
38
-
-
0029934215
-
Management of pulmonary disease in patients with cystic fibrosis
-
DOI 10.1056/NEJM199607183350307
-
RAMSEY B.W. (1996). Management of pulmonary disease in patients with cystic fibrosis. N. Engl. J. Med. 335, 179-188. (Pubitemid 26249456)
-
(1996)
New England Journal of Medicine
, vol.335
, Issue.3
, pp. 179-188
-
-
Ramsey, B.W.1
-
39
-
-
8644256676
-
Characterization of bacterial community diversity in cystic fibrosis lung infections by use of 16S ribosomal DNA terminal restriction fragment length polymorphism profiling
-
ROGERS G.B., CARROLL M.P., SERISIER D.J., HOCKEY P.M., JONES G., BRUCE K.D. (2004). Characterization of bacterial community diversity in cystic fibrosis lung infections by use of 16S ribosomal DNA terminal restriction fragment length polymorphism profiling. J. Clin. Microbiol. 42, 5176-5183.
-
(2004)
J. Clin. Microbiol.
, vol.42
, pp. 5176-5183
-
-
Rogers, G.B.1
Carroll, M.P.2
Serisier, D.J.3
Hockey, P.M.4
Jones, G.5
Bruce, K.D.6
-
40
-
-
33746255217
-
Use of 16S rRNA profiling by terminal restriction fragment length polymorphism analysis to compare bacterial communities in sputum and mouthwash samples from patients with cystic fibrosis
-
ROGERS G.B., CARROLL M.P., SERISIER D.J., HOCKEY P.M., JONES G., KEHAGIA V., CONNETT G.J., BRUCE K.D. (2006). Use of 16S rRNA profiling by terminal restriction fragment length polymorphism analysis to compare bacterial communities in sputum and mouthwash samples from patients with cystic fibrosis. J. Clin. Microbiol. 44, 2601-2604.
-
(2006)
J. Clin. Microbiol.
, vol.44
, pp. 2601-2604
-
-
Rogers, G.B.1
Carroll, M.P.2
Serisier, D.J.3
Hockey, P.M.4
Jones, G.5
Kehagia, V.6
Connett, G.J.7
Bruce, K.D.8
-
41
-
-
0034764166
-
Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis
-
DOI 10.1002/ppul.1144
-
ROSENFELD M., GIBSON R.L., MCNAMARA S., EMERSON J., BURNS J.L., CASTILE R., HIATT P., MCCOY K., WILSON C.B., INGLIS A., SMITH A., MARTIN T.R., RAMSEY B.W. (2001). Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis. Pediatr. Pulmunol. 32, 356-366. (Pubitemid 33015652)
-
(2001)
Pediatric Pulmonology
, vol.32
, Issue.5
, pp. 356-366
-
-
Rosenfeld, M.1
Gibson, R.L.2
McNamara, S.3
Emerson, J.4
Burns, J.L.5
Castile, R.6
Hiatt, P.7
McCoy, K.8
Wilson, C.B.9
Inglis, A.10
Smith, A.11
Martin, T.R.12
Ramsey, B.W.13
-
42
-
-
1642556721
-
Infection control in cystic fibrosis
-
SAIMAN L., SIEGEL J. (2004). Infection Control in Cystic Fibrosis. Clin. Microbiol. Rev. 17, 57-71.
-
(2004)
Clin. Microbiol. Rev.
, vol.17
, pp. 57-71
-
-
Saiman, L.1
Siegel, J.2
-
43
-
-
0027263474
-
Antibacterial activity of meropenem and selected comparative agents against anaerobic bacteria at seven North American centres
-
SHEIKH W., PITKIN D.H., NADLER H. (1993). Antibacterial activity of meropenem and selected comparative agents against anaerobic bacteria at seven North American centres. Clin. Infect. Dis. 16, 361-366.
-
(1993)
Clin. Infect. Dis.
, vol.16
, pp. 361-366
-
-
Sheikh, W.1
Pitkin, D.H.2
Nadler, H.3
-
44
-
-
55549087586
-
Anaerobic bacterial infection in patients with cystic fibrosis
-
TAI A., RANGANATH S. (2008). Anaerobic bacterial infection in patients with cystic fibrosis. Am. J. Respir. Crit. Care Med. 178, 994.
-
(2008)
Am. J. Respir. Crit. Care Med.
, vol.178
, pp. 994
-
-
Tai, A.1
Ranganath, S.2
-
45
-
-
0036320181
-
Alcaligenes infection in cystic fibrosis
-
TAN K., CONWAY S.P., BROWNLEE K.G., ETHERINGTON C., PECKHAM D.G. (2002). Alcaligenes infection in cystic fibrosis. Pediatr. Pulmonol. 34, 101-104.
-
(2002)
Pediatr. Pulmonol.
, vol.34
, pp. 101-104
-
-
Tan, K.1
Conway, S.P.2
Brownlee, K.G.3
Etherington, C.4
Peckham, D.G.5
-
46
-
-
0021325047
-
Cultures of thoracotomy confirm usefulness of sputum cultures in cystic fibrosis
-
THOMASSEN M.J., KLINGER J.D., BADGER S.J., VAN HEECKEREN D.W., STERN R.C. (1984). Cultures of thoracotomy confirm usefulness of sputum cultures in cystic fibrosis. J. Pediatr. 104, 352-356.
-
(1984)
J. Pediatr.
, vol.104
, pp. 352-356
-
-
Thomassen, M.J.1
Klinger, J.D.2
Badger, S.J.3
Van Heeckeren, D.W.4
Stern, R.C.5
-
47
-
-
42949105490
-
Detection of anaerobic bacteria in high numbers in sputum from patients with cystic fibrosis
-
TUNNEY M.M., FIELD T.R., MORIARTY T.E., PATRICK S., DOERING G., MUHLEBACH M.S., WOLFGANG M.C., BOUCHER R., GILPIN D.F., MCDOWELL A., ELBORN J.S. (2008). Detection of anaerobic bacteria in high numbers in sputum from patients with cystic fibrosis. Am. J. Respir. Crit. Care Med. 177, 995-1001.
-
(2008)
Am. J. Respir. Crit. Care Med.
, vol.177
, pp. 995-1001
-
-
Tunney, M.M.1
Field, T.R.2
Moriarty, T.E.3
Patrick, S.4
Doering, G.5
Muhlebach, M.S.6
Wolfgang, M.C.7
Boucher, R.8
Gilpin, D.F.9
Mcdowell, A.10
Elborn, J.S.11
-
48
-
-
0027162649
-
Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
-
DOI 10.1016/0092-8674(93)90353-R
-
WELSH M.J., SMITH A.E. (1993). Molecular Mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell. 73, 1251-1254. (Pubitemid 23201140)
-
(1993)
Cell
, vol.73
, Issue.7
, pp. 1251-1254
-
-
Welsh, M.J.1
Smith, A.E.2
-
49
-
-
0023831669
-
In vitro activity of cefoperazone plus sulbactam compared with that of other antimicrobial agents against anaerobic bacteria
-
WEXLER H.M., FINEGOLD S.M. (1988). In vitro activity of cefoperazone plus sulbactam compared with that of other antimicrobial agents against anaerobic bacteria. Antimicrob. Agents Chemoter. 32 (3), 403-406.
-
(1988)
Antimicrob. Agents Chemoter.
, vol.32
, Issue.3
, pp. 403-406
-
-
Wexler, H.M.1
Finegold, S.M.2
-
51
-
-
0036167851
-
Effects of reduced mucus oxygen concentration in airway Pseudomonas infection of cystic fibrosis patients
-
WORLITZSCH D., TARRAN R., ULRICH M., SCHWAB U., CEKICKI A., MEYER K.C., BIRRER P., BELLON G., BERGER J., WEISS T., BOTZENHART K., YANKASKAS J.R., RANDELL S., BOUCHER R.C., DORING G. (2002). Effects of reduced mucus oxygen concentration in airway Pseudomonas infection of cystic fibrosis patients. J. Clin. Invest. 109 (3), 317-325.
-
(2002)
J. Clin. Invest.
, vol.109
, Issue.3
, pp. 317-325
-
-
Worlitzsch, D.1
Tarran, R.2
Ulrich, M.3
Schwab, U.4
Cekicki, A.5
Meyer, K.C.6
Birrer, P.7
Bellon, G.8
Berger, J.9
Weiss, T.10
Botzenhart, K.11
Yankaskas, J.R.12
Randell, S.13
Boucher, R.C.14
Doring, G.15
-
52
-
-
65949091603
-
Antibiotic-resistant obligate anaerobes during exacerbations of cystic fibrosis patients
-
WORLITZSCH D., RJNTELEN C., BOHM K., WOLLSCHLAGER B., MERKEL N., BORNEFF-LIPP M., DORING G. (2009). Antibiotic-resistant obligate anaerobes during exacerbations of cystic fibrosis patients. Clin. Microbiol. Infect. 15 (5), 454-460.
-
(2009)
Clin. Microbiol. Infect.
, vol.15
, Issue.5
, pp. 454-460
-
-
Worlitzsch, D.1
Rjntelen, C.2
Bohm, K.3
Wollschlager, B.4
Merkel, N.5
Borneff-Lipp, M.6
Doring, G.7
-
53
-
-
0347777343
-
Pseudomonas aeruginosa anaerobic respiration in biofilms: Relationships to cystic fibrosis pathogenesis
-
YOON S.S., HENNIGAN R.F., HILLIARD G.M., OCHSNER U.A., PARVATIYAR K., KAMANI M.C., ALLEN H.L., DEKIEVIT T.R., GARDNER P.R., SCHWAB U., ROWE J.J., IGLEWSKI B.H., MCDERMOTT T.R., MASON R.P., WOZNIAK D. J., HANCOCK R.E., PARSEK M.R., NOAH T.L., BOUCHER R.C., HASSETT D.J. (2002). Pseudomonas aeruginosa anaerobic respiration in biofilms: relationships to cystic fibrosis pathogenesis. Dev. Cell. 3 (4), 593-603.
-
(2002)
Dev. Cell.
, vol.3
, Issue.4
, pp. 593-603
-
-
Yoon, S.S.1
Hennigan, R.F.2
Hilliard, G.M.3
Ochsner, U.A.4
Parvatiyar, K.5
Kamani, M.C.6
Allen, H.L.7
Dekievit, T.R.8
Gardner, P.R.9
Schwab, U.10
Rowe, J.J.11
Iglewski, B.H.12
Mcdermott, T.R.13
Mason, R.P.14
Wozniak, D.J.15
Hancock, R.E.16
Parsek, M.R.17
Noah, T.L.18
Boucher, R.C.19
Hassett, D.J.20
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