-
1
-
-
0029934215
-
Management of pulmonary disease in patients with cystic fibrosis
-
DOI 10.1056/NEJM199607183350307
-
Ramsey BW. Management of pulmonary disease in patients with cystic fibrosis. N. Engl. J. Med. 335(3), 179-188 (1996). (Pubitemid 26249456)
-
(1996)
New England Journal of Medicine
, vol.335
, Issue.3
, pp. 179-188
-
-
Ramsey, B.W.1
-
2
-
-
0031458028
-
Incidence, population, and survival of cystic fibrosis in the UK, 1968- 95
-
Dodge JA, Morison S, Lewis PA et al. Incidence, population, and survival of cystic fibrosis in the UK, 1968-1995. Arch. Dis. Child. 77(6), 493-496 (1997). (Pubitemid 28016366)
-
(1997)
Archives of Disease in Childhood
, vol.77
, Issue.6
, pp. 493-496
-
-
Dodge, J.A.1
Morison, S.2
Lewis, P.A.3
Coles, E.C.4
Geddes, D.5
Russell, G.6
Littlewood, J.M.7
Scott, M.T.8
-
3
-
-
84856484379
-
The Cystic Fibrosis Trust's Clinical Standards and Accreditation Group. Standards for the clinical care of children and adults with cystic fibrosis in the UK 2001
-
The Cystic Fibrosis Trust's Clinical Standards and Accreditation Group. Standards for the clinical care of children and adults with cystic fibrosis in the UK 2001. CF Trust 1-56 (2001).
-
(2001)
CF Trust
, pp. 1-56
-
-
-
4
-
-
33845992179
-
Evidence for airway surface dehydration as the initiating event in CF airway disease
-
DOI 10.1111/j.1365-2796.2006.01744.x
-
Boucher RC. Evidence for airway surface dehydration as the initiating event in CF airway disease. J. Intern. Med. 261(1), 5-16 (2007). (Pubitemid 46046468)
-
(2007)
Journal of Internal Medicine
, vol.261
, Issue.1
, pp. 5-16
-
-
Boucher, R.C.1
-
7
-
-
2442645035
-
Finally, mice with CF lung disease
-
DOI 10.1038/nm0504-452
-
Frizzell RA, Pilewski JM. Finally, mice with CF lung disease. Nat. Med. 10(5), 452-454 (2004). (Pubitemid 38667896)
-
(2004)
Nature Medicine
, vol.10
, Issue.5
, pp. 452-454
-
-
Frizzell, R.A.1
Pilewski, J.M.2
-
8
-
-
2442718786
-
+ absorption produces cystic fibrosis-like lung disease in mice
-
DOI 10.1038/nm1028
-
Mall M, Grubb BR, Harkema JR, O'Neal WK, Boucher RC. Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice. Nat. Med. 10(5), 487-493 (2004). (Pubitemid 38667907)
-
(2004)
Nature Medicine
, vol.10
, Issue.5
, pp. 487-493
-
-
Mall, M.1
Grubb, B.R.2
Harkema, J.R.3
O'Neal, W.K.4
Boucher, R.C.5
-
9
-
-
0037460729
-
Cystic fibrosis
-
DOI 10.1016/S0140-6736(03)12567-6
-
Ratjen F, Doring G. Cystic fibrosis. Lancet 361(9358), 681-689 (2003). (Pubitemid 36246556)
-
(2003)
Lancet
, vol.361
, Issue.9358
, pp. 681-689
-
-
Ratjen, F.1
Doring, G.2
-
10
-
-
0016416841
-
Defense mechanisms of the lungs
-
Cohen AB, Gold WM. Defense mechanisms of the lungs. Annu. Rev. Physiol. 37(1), 325-350 (1975).
-
(1975)
Annu. Rev. Physiol.
, vol.37
, Issue.1
, pp. 325-350
-
-
Cohen, A.B.1
Gold, W.M.2
-
11
-
-
0030027655
-
In vivo effects of recombinant human DNase I on sputum in patients with cystic fibrosis
-
Shah PL, Scott SF, Knight RA, Marriott C, Ranasinha C, Hodson ME. In vivo effects of recombinant human DNase I on sputum in patients with cystic fibrosis. Thorax 51(2), 119-125 (1996). (Pubitemid 26060647)
-
(1996)
Thorax
, vol.51
, Issue.2
, pp. 119-125
-
-
Shah, P.L.1
Scott, S.F.2
Knight, R.A.3
Marriott, C.4
Ranasinha, C.5
Hodson, M.E.6
-
12
-
-
0028129568
-
Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis
-
DOI 10.1056/NEJM199409083311003
-
Fuchs HJ, Borowitz DS, Christiansen DH et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. N. Engl. J. Med. 331(10), 637-642 (1994). (Pubitemid 24276863)
-
(1994)
New England Journal of Medicine
, vol.331
, Issue.10
, pp. 637-642
-
-
Fuchs, H.J.1
Borowitz, D.S.2
Christiansen, D.H.3
Morris, E.M.4
Nash, M.L.5
Ramsey, B.W.6
Rosenstein, B.J.7
Smith, A.L.8
Wohl, M.E.9
-
13
-
-
0035666058
-
A two-year randomized, placebo-controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities
-
DOI 10.1067/mpd.2001.118570
-
Quan JM, Tiddens HAWM, Sy JP et al. A two-year randomized, placebo-controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities. J. Pediatr. 139(6), 813-820 (2001). (Pubitemid 34014460)
-
(2001)
Journal of Pediatrics
, vol.139
, Issue.6
, pp. 813-820
-
-
Quan, J.M.1
Tiddens, H.A.W.M.2
Sy, J.P.3
McKenzie, S.G.4
Montgomery, M.D.5
Robinson, P.J.6
Wohl, M.E.B.7
Konstan, M.W.8
-
14
-
-
0029921953
-
Effects of 12-week administration of dornase alfa in patients with advanced cystic fibrosis lung disease
-
Mccoy K, Hamilton S, Johnson C. Effects of 12-week administration of dornase alfa in patients with advanced cystic fibrosis lung disease. Chest 110(4), 889-895 (1996). (Pubitemid 26347599)
-
(1996)
Chest
, vol.110
, Issue.4
, pp. 889-895
-
-
McCoy, K.1
Hamilton, S.2
Johnson, C.3
-
15
-
-
79955909454
-
For the Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Clinical use of dornase alfa is associated with a slower rate of FEV1 decline in cystic fibrosis
-
Konstan MW, Wagener JS, Pasta DJ et al.; for the Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Clinical use of dornase alfa is associated with a slower rate of FEV1 decline in cystic fibrosis. Pediatr. Pulmonol. 46(6), 545-553 (2011).
-
(2011)
Pediatr. Pulmonol
, vol.46
, Issue.6
, pp. 545-553
-
-
Konstan, M.W.1
Wagener, J.S.2
Pasta, D.J.3
-
16
-
-
79952522208
-
Improved survival at low lung function in cystic fibrosis: Cohort study from 1990 to 2007
-
George PM, Banya W, Pareek N et al. Improved survival at low lung function in cystic fibrosis: Cohort study from 1990 to 2007. BMJ 342, d1008 (2011).
-
(2011)
BMJ
, vol.342
-
-
George, P.M.1
Banya, W.2
Pareek, N.3
-
18
-
-
69549135253
-
Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus
-
Heijerman H, Westerman E, Conway S, Touw D. Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus. J. Cyst. Fibros. 8(5), 295-315 (2009).
-
(2009)
J. Cyst. Fibros.
, vol.8
, Issue.5
, pp. 295-315
-
-
Heijerman, H.1
Westerman, E.2
Conway, S.3
Touw, D.4
-
19
-
-
0001609666
-
The in vitro reduction in viscocity of human tracheobronchial secretions by acetylcysteine
-
Scheffner AL, Medler EM, Jacobs LW, Sarett HP. The in vitro reduction in viscocity of human tracheobronchial secretions by acetylcysteine. Am. Rev. Respir. Dis. 90, 721-729 (1964).
-
(1964)
Am. Rev. Respir. Dis.
, vol.90
, pp. 721-729
-
-
Scheffner, A.L.1
Medler, E.M.2
Jacobs, L.W.3
Sarett, H.P.4
-
20
-
-
44949116170
-
Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis
-
Nash EF, Stephenson A, Atjen F, Tullis E. Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis. Cochrane Database Syst. Rev. 21(1), CD007168 (2009).
-
(2009)
Cochrane Database Syst. Rev.
, vol.21
, Issue.1
-
-
Nash, E.F.1
Stephenson, A.2
Atjen, F.3
Tullis, E.4
-
21
-
-
30944466084
-
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
-
DOI 10.1056/NEJMoa043900
-
Elkins MR, Robinson M, Rose BR et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N. Engl. J. Med. 354(3), 229-240 (2006). (Pubitemid 43113028)
-
(2006)
New England Journal of Medicine
, vol.354
, Issue.3
, pp. 229-240
-
-
Elkins, M.R.1
Robinson, M.2
Rose, B.R.3
Harbour, C.4
Moriarty, C.P.5
Marks, G.B.6
Belousova, E.G.7
Xuan, W.8
Bye, P.T.P.9
-
23
-
-
0346121620
-
Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis
-
Gustafsson PM, Aurora P, Lindblad A. Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis. Eur. Respir. J. 22(6), 972-979 (2003). (Pubitemid 37540651)
-
(2003)
European Respiratory Journal
, vol.22
, Issue.6
, pp. 972-979
-
-
Gustafsson, P.M.1
Aurora, P.2
Lindblad, A.3
-
24
-
-
39049084491
-
Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis
-
DOI 10.1136/thx.2007.077784
-
Gustafsson PM, De Jong PA, Tiddens HAWM, Lindblad A. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis. Thorax 63(2), 129-134 (2008). (Pubitemid 351236476)
-
(2008)
Thorax
, vol.63
, Issue.2
, pp. 129-134
-
-
Gustafsson, P.M.1
De Jong, P.A.2
Tiddens, H.A.W.M.3
Lindblad, A.4
-
25
-
-
79952211206
-
Denufosol tetrasodium in patients with cystic fibrosis and normal to mildly impaired lung function
-
Accurso FJ, Moss RB, Wilmott RW et al. Denufosol tetrasodium in patients with cystic fibrosis and normal to mildly impaired lung function. Am. J. Respir. Crit. Care Med. 183(5), 627-634 (2011).
-
(2011)
Am. J. Respir. Crit. Care Med.
, vol.183
, Issue.5
, pp. 627-634
-
-
Accurso, F.J.1
Moss, R.B.2
Wilmott, R.W.3
-
26
-
-
79956372057
-
-
Joint Formulary Committee (Ed.). BMJ Group and Pharmaceutical Press, London, UK
-
Joint Formulary Committee. British National Formulary 60. Joint Formulary Committee (Ed.). BMJ Group and Pharmaceutical Press, London, UK (2010).
-
(2010)
Joint Formulary Committee. British National Formulary
, vol.60
-
-
-
27
-
-
61549111538
-
Comparison of mannitol and methacholine to predict exercise-induced bronchoconstriction and a clinical diagnosis of asthma
-
Anderson S, Charlton B, Weiler J et al. Comparison of mannitol and methacholine to predict exercise-induced bronchoconstriction and a clinical diagnosis of asthma. Respir. Res. 10(1), 4 (2009).
-
(2009)
Respir. Res.
, vol.10
, Issue.1
, pp. 4
-
-
Anderson, S.1
Charlton, B.2
Weiler, J.3
-
28
-
-
28844485771
-
The safety and efficacy of inhaled dry powder mannitol as a bronchial provocation test for airway hyperresponsiveness: A Phase 3 comparison study with hypertonic 4.5%) saline
-
Brannan J, Anderson S, Perry C et al. The safety and efficacy of inhaled dry powder mannitol as a bronchial provocation test for airway hyperresponsiveness: A Phase 3 comparison study with hypertonic (4.5%) saline. Respir. Res. 6(1), 144 (2005).
-
(2005)
Respir. Res.
, Issue.1
, pp. 144
-
-
Brannan, J.1
Anderson, S.2
Perry, C.3
-
29
-
-
80355127141
-
Inhaled dry powder mannitol in cystic fibrosis: An efficacy and safety study
-
Bilton D, Robinson P, Cooper P et al. Inhaled dry powder mannitol in cystic fibrosis: An efficacy and safety study. Eur. Respir. J. 38(5), 1071-1080 (2011).
-
(2011)
Eur. Respir. J.
, vol.38
, Issue.5
, pp. 1071-1080
-
-
Bilton, D.1
Robinson, P.2
Cooper, P.3
-
30
-
-
84856501625
-
-
Investigator's Brochure: Bronchitol (inhaled dry powder mannitol for airway disease). Pharmaxis (10), section 4-6 (2010).
-
(2010)
Pharmaxis
, vol.10
, pp. 4-6
-
-
-
31
-
-
0025306375
-
Goblet cells secretion and mucogenesis
-
Verdugo P. Goblet cells secretion and mucogenesis. Annu. Rev. Physiol. 52(1), 157-176 (1990). (Pubitemid 20103532)
-
(1990)
Annual Review of Physiology
, vol.52
, pp. 157-176
-
-
Verdugo, P.1
-
32
-
-
0037027914
-
Pharmacological approaches to discovery and development of new mucolytic agents
-
DOI 10.1016/S0169-409X(02)00156-4, PII S0169409X02001564
-
King M, Rubin B. Pharmacological approaches to discovery and development of new mucolytic agents. Adv. Drug Deliv. Rev. 54(11), 1475-1490 (2002). (Pubitemid 35375771)
-
(2002)
Advanced Drug Delivery Reviews
, vol.54
, Issue.11
, pp. 1475-1490
-
-
King, M.1
Rubin, B.K.2
-
33
-
-
0031018453
-
Sodium chloride increases the ciliary transportability of cystic fibrosis and bronchiectasis sputum on the mucus-depleted bovine trachea
-
Wills PJ, Hall RL, Chan W, Cole PJ. Sodium chloride increases the ciliary transportability of cystic fibrosis and bronchiectasis sputum on the mucusdepleted bovine trachea. J. Clin. Invest. 99(1), 9-13 (1997). (Pubitemid 27058287)
-
(1997)
Journal of Clinical Investigation
, vol.99
, Issue.1
, pp. 9-13
-
-
Wills, P.J.1
Hall, R.L.2
Chan, W.-M.3
Cole, P.J.4
-
34
-
-
0042380075
-
Evidence of mast cell activation and leukotriene release after mannitol inhalation
-
DOI 10.1183/09031936.03.00113403
-
Brannan JD, Gulliksson M, Anderson SD, Chew N, Kumlin M. Evidence of mast cell activation and leukotriene release after mannitol inhalation. Eur. Respir. J. 22(3), 491-496 (2003). (Pubitemid 37098931)
-
(2003)
European Respiratory Journal
, vol.22
, Issue.3
, pp. 491-496
-
-
Brannan, J.D.1
Gulliksson, M.2
Anderson, S.D.3
Chew, N.4
Kumlin, M.5
-
35
-
-
0032834277
-
The effect of inhaled mannitol on bronchial mucus clearance in cystic fibrosis patients: A pilot study
-
DOI 10.1034/j.1399-3003.1999.14c30.x
-
Robinson M, Daviskas E, Eberl S et al. The effect of inhaled mannitol on bronchial mucus clearance in cystic fibrosis patients: A pilot study. Eur. Respir. J. 14(3), 678-685 (1999). (Pubitemid 29479736)
-
(1999)
European Respiratory Journal
, vol.14
, Issue.3
, pp. 678-685
-
-
Robinson, M.1
Daviskas, E.2
Eberl, S.3
Baker, J.4
Chan, H.-K.5
Anderson, S.D.6
Bye, P.T.P.7
-
36
-
-
0031444391
-
Inhalation of dry-powder mannitol increases mucociliary clearance
-
DOI 10.1183/09031936.97.10112449
-
Daviskas E, Anderson SD, Brannan JD, Chan HK, Eberl S, Bautovich G. Inhalation of dry-powder mannitol increases mucociliary clearance. Eur. Respir. J. 10(11), 2449-2454 (1997). (Pubitemid 28048614)
-
(1997)
European Respiratory Journal
, vol.10
, Issue.11
, pp. 2449-2454
-
-
Daviskas, E.1
Anderson, S.D.2
Brannan, J.D.3
Chan, H.-K.4
Eberl, S.5
Bautovich, G.6
-
37
-
-
0033039551
-
Inhalation of dry powder mannitol improves clearance of mucus in patients with bronchiectasis
-
Daviskas E, Anderson S, Eberl S, Chan HK, Bautovich G. Inhalation of dry powder mannitol improves clearance of mucus in patients with bronchiectasis. Am. J. Respir. Crit. Care Med. 159(6), 1843-1848 (1999). (Pubitemid 29275053)
-
(1999)
American Journal of Respiratory and Critical Care Medicine
, vol.159
, Issue.6
, pp. 1843-1848
-
-
Daviskas, E.1
Anderson, S.D.2
Eberl, S.3
Chan, H.-K.4
Bautovich, G.5
-
38
-
-
0035110224
-
The 24-h effect of mannitol on the clearance of mucus in patients with bronchiectasis
-
DOI 10.1378/chest.119.2.414
-
Daviskas E, Anderson SD, Eberl S, Chan HK, Young IH. The 24-h effect of mannitol on the clearance of mucus in patients with bronchiectasis. Chest 119(2), 414-421 (2001). (Pubitemid 32163751)
-
(2001)
Chest
, vol.119
, Issue.2
, pp. 414-421
-
-
Daviskas, E.1
Anderson, S.D.2
Eberl, S.3
Chan, H.-K.4
Young, I.H.5
-
39
-
-
76449101506
-
Effect of mannitol and repetitive coughing on the sputum properties in bronchiectasis
-
Daviskas E, Anderson SD, Young IH. Effect of mannitol and repetitive coughing on the sputum properties in bronchiectasis. Respir. Med. 104(3), 371-377 (2010).
-
(2010)
Respir. Med.
, vol.104
, Issue.3
, pp. 371-377
-
-
Daviskas, E.1
Anderson, S.D.2
Young, I.H.3
-
40
-
-
42949178050
-
Effect of increasing doses of mannitol on mucus clearance in patients with bronchiectasis
-
Daviskas E, Anderson SD, Eberl S, Young IH. Effect of increasing doses of mannitol on mucus clearance in patients with bronchiectasis. Eur. Respir. J. 31(4), 765-772 (2008).
-
(2008)
Eur. Respir. J.
, vol.31
, Issue.4
, pp. 765-772
-
-
Daviskas, E.1
Anderson, S.D.2
Eberl, S.3
Young, I.H.4
-
41
-
-
14844292681
-
Inhaled mannitol for the treatment of mucociliary dysfunction in patients with bronchiectasis: Effect on lung function, health status and sputum
-
DOI 10.1111/j.1440-1843.2005.00659.x
-
Daviskas E, Anderson SD, Gomes K et al. Inhaled mannitol for the treatment of mucociliary dysfunction in patients with bronchiectasis: Effect on lung function, health status and sputum. Respirology 10(1), 46-56 (2005). (Pubitemid 40343762)
-
(2005)
Respirology
, vol.10
, Issue.1
, pp. 46-56
-
-
Daviskas, E.1
Anderson, S.D.2
Gomes, K.3
Briffa, P.4
Cochrane, B.5
Chan, H.-K.6
Young, I.H.7
Rubin, B.K.8
-
42
-
-
77951890116
-
A randomised, placebocontrolled trial of inhaled mannitol in patients with bronchiectasis
-
Bilton D, Daviskas E, Jaques A, Anderson S, Charlton B. A randomised, placebocontrolled trial of inhaled mannitol in patients with bronchiectasis. Am. J. Respir. Crit. Care Med. 179, A3221 (2009).
-
(2009)
Am. J. Respir. Crit. Care Med.
, vol.179
-
-
Bilton, D.1
Daviskas, E.2
Jaques, A.3
Anderson, S.4
Charlton, B.5
-
43
-
-
44649166466
-
Inhaled mannitol improves lung function in cystic fibrosis
-
DOI 10.1378/chest.07-2294
-
Jaques A, Daviskas E, Turton JA et al. Inhaled mannitol improves lung function in cystic fibrosis. Chest 133(6), 1388-1396 (2008). (Pubitemid 351892995)
-
(2008)
Chest
, vol.133
, Issue.6
, pp. 1388-1396
-
-
Jaques, A.1
Daviskas, E.2
Turton, J.A.3
McKay, K.4
Cooper, P.5
Stirling, R.G.6
Robertson, C.F.7
Bye, P.T.P.8
LeSouef, P.N.9
Shadbolt, B.10
Anderson, S.D.11
Charlton, B.12
-
44
-
-
77950787429
-
Inhaled mannitol improves the hydration and surface properties of sputum in patients with cystic fibrosis
-
Daviskas E, Anderson SD, Jaques A, Charlton B. Inhaled mannitol improves the hydration and surface properties of sputum in patients with cystic fibrosis. Chest 137(4), 861-868 (2010).
-
(2010)
Chest
, vol.137
, Issue.4
, pp. 861-868
-
-
Daviskas, E.1
Anderson, S.D.2
Jaques, A.3
Charlton, B.4
-
45
-
-
73449118258
-
Comparison of inhaled mannitol, daily rhDNase and a combination of both in children with cystic fibrosis: A randomised trial
-
Minasian C, Wallis C, Metcalfe C, Bush A. Comparison of inhaled mannitol, daily rhDNase and a combination of both in children with cystic fibrosis: A randomised trial. Thorax 65(1), 51-56 (2010).
-
(2010)
Thorax
, vol.65
, Issue.1
, pp. 51-56
-
-
Minasian, C.1
Wallis, C.2
Metcalfe, C.3
Bush, A.4
-
46
-
-
57349176546
-
Bronchial provocation testing with dry powder mannitol in children with cystic fibrosis
-
Minasian C, Wallis C, Metcalfe C, Bush A. Bronchial provocation testing with dry powder mannitol in children with cystic fibrosis. Pediatr. Pulmonol. 43(11), 1078-1084 (2008).
-
(2008)
Pediatr. Pulmonol.
, vol.43
, Issue.11
, pp. 1078-1084
-
-
Minasian, C.1
Wallis, C.2
Metcalfe, C.3
Bush, A.4
-
47
-
-
78651452280
-
Inhaled mannitol in patients with cystic fibrosis: A randomised open-label dose response trial
-
Teper A, Jaques A, Charlton B. Inhaled mannitol in patients with cystic fibrosis: A randomised open-label dose response trial. J. Cyst. Fibros. 10(1), 1-8 (2011).
-
(2011)
J. Cyst. Fibros.
, vol.10
, Issue.1
, pp. 1-8
-
-
Teper, A.1
Jaques, A.2
Charlton, B.3
-
48
-
-
84856485746
-
Joint FAO/ WHO Expert Committee on Food Additives. 616
-
Joint FAO/WHO Expert Committee on Food Additives. 616. Mannitol. WHO Food Additives Series 21 (1986).
-
(1986)
Mannitol. WHO Food Additives Series
, vol.21
-
-
-
49
-
-
51149120169
-
Plant host and sugar alcohol induced exopolysaccharide biosynthesis in the Burkholderia cepacia complex
-
Bartholdson SJ, Brown AR, Mewburn BR et al. Plant host and sugar alcohol induced exopolysaccharide biosynthesis in the Burkholderia cepacia complex. Microbiology 154(8), 2513-2521 (2008).
-
(2008)
Microbiology
, vol.154
, Issue.8
, pp. 2513-2521
-
-
Bartholdson, S.J.1
Brown, A.R.2
Mewburn, B.R.3
|