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Results: 1 to 20 of 64

1.

Risk of hemoptysis in cystic fibrosis clinical trials: A retrospective cohort study.

Thompson V, Mayer-Hamblett N, Kloster M, Bilton D, Flume PA.

J Cyst Fibros. 2015 Feb 25. pii: S1569-1993(15)00040-5. doi: 10.1016/j.jcf.2015.02.003. [Epub ahead of print]

PMID:
25725985
2.

A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients.

Stuart Elborn J, Geller DE, Conrad D, Aaron SD, Smyth AR, Fischer R, Kerem E, Bell SC, Loutit JS, Dudley MN, Morgan EE, VanDevanter DR, Flume PA.

J Cyst Fibros. 2015 Jan 12. pii: S1569-1993(14)00310-5. doi: 10.1016/j.jcf.2014.12.013. [Epub ahead of print]

PMID:
25592656
3.

Clinical applications of pulmonary delivery of antibiotics.

Flume PA, VanDevanter DR.

Adv Drug Deliv Rev. 2014 Oct 22. pii: S0169-409X(14)00217-8. doi: 10.1016/j.addr.2014.10.009. [Epub ahead of print] Review.

PMID:
25453268
4.

A preliminary quality of life questionnaire-bronchiectasis: a patient-reported outcome measure for bronchiectasis.

Quittner AL, Marciel KK, Salathe MA, O'Donnell AE, Gotfried MH, Ilowite JS, Metersky ML, Flume PA, Lewis SA, McKevitt M, Montgomery AB, O'Riordan TG, Barker AF.

Chest. 2014 Aug;146(2):437-48. doi: 10.1378/chest.13-1891. Review. Erratum in: Chest. 2014 Nov;146(5):1422.

PMID:
24626872
5.

Lung clearance index. A potential quantitative tool to assess treatment response in bronchiectasis?

Hill AT, Flume PA.

Am J Respir Crit Care Med. 2014 Mar 1;189(5):510-1. doi: 10.1164/rccm.201401-0129ED. No abstract available.

PMID:
24579835
6.

Timing of inhaled tobramycin affects assessment of intravenous tobramycin pharmacokinetic monitoring.

Stenbit AE, Bullington WM, Heh JL, Flume PA.

J Cyst Fibros. 2013 Jul;12(4):403-6. doi: 10.1016/j.jcf.2012.11.007. Epub 2012 Dec 20.

PMID:
23266092
7.

Pooled analysis of two large randomised phase III inhaled mannitol studies in cystic fibrosis.

Bilton D, Bellon G, Charlton B, Cooper P, De Boeck K, Flume PA, Fox HG, Gallagher CG, Geller DE, Haarman EG, Hebestreit HU, Kolbe J, Lapey A, Robinson P, Wu J, Zuckerman JB, Aitken ML; CF301 and CF302 Investigators.

J Cyst Fibros. 2013 Jul;12(4):367-76. doi: 10.1016/j.jcf.2012.11.002. Epub 2012 Dec 9.

PMID:
23234802
8.

State of progress in treating cystic fibrosis respiratory disease.

Flume PA, Van Devanter DR.

BMC Med. 2012 Aug 10;10:88. doi: 10.1186/1741-7015-10-88. Review.

9.

Ivacaftor in subjects with cystic fibrosis who are homozygous for the F508del-CFTR mutation.

Flume PA, Liou TG, Borowitz DS, Li H, Yen K, OrdoƱez CL, Geller DE; VX 08-770-104 Study Group.

Chest. 2012 Sep;142(3):718-24.

10.

Chronic cystic fibrosis respiratory infections: where do we go from here? Introduction.

Flume PA.

Respir Med. 2011 Dec;105 Suppl 2:S1. doi: 10.1016/S0954-6111(11)00444-6. No abstract available.

11.

Applying clinical outcome variables to appropriate aerosolized antibiotics for the treatment of patients with cystic fibrosis.

VanDevanter DR, Ballmann M, Flume PA.

Respir Med. 2011 Dec;105 Suppl 2:S18-23. doi: 10.1016/S0954-6111(11)70023-3.

12.

Long-term inhaled dry powder mannitol in cystic fibrosis: an international randomized study.

Aitken ML, Bellon G, De Boeck K, Flume PA, Fox HG, Geller DE, Haarman EG, Hebestreit HU, Lapey A, Schou IM, Zuckerman JB, Charlton B; CF302 Investigators.

Am J Respir Crit Care Med. 2012 Mar 15;185(6):645-52. doi: 10.1164/rccm.201109-1666OC. Epub 2011 Dec 28.

PMID:
22198974
13.

Prerenal azotemia from excessive sweating in an adult with a cystic fibrosis gene mutation.

Tomov SV, Flume PA, Stenbit AE, Ullian ME.

Indian J Nephrol. 2011 Jul;21(3):194-7. doi: 10.4103/0971-4065.82637.

14.

Pulmonary exacerbations in cystic fibrosis.

Stenbit AE, Flume PA.

Curr Opin Pulm Med. 2011 Nov;17(6):442-7. doi: 10.1097/MCP.0b013e32834b8c04. Review.

PMID:
21881509
15.

Update in cystic fibrosis 2010.

Mogayzel PJ Jr, Flume PA.

Am J Respir Crit Care Med. 2011 Jun 15;183(12):1620-4. doi: 10.1164/rccm.201102-0275UP. Review. No abstract available.

PMID:
21693717
16.

Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa.

Geller DE, Flume PA, Staab D, Fischer R, Loutit JS, Conrad DJ; Mpex 204 Study Group.

Am J Respir Crit Care Med. 2011 Jun 1;183(11):1510-6. doi: 10.1164/rccm.201008-1293OC. Epub 2011 Feb 25.

PMID:
21471106
17.

Pneumothorax in cystic fibrosis.

Flume PA.

Curr Opin Pulm Med. 2011 Jul;17(4):220-5. doi: 10.1097/MCP.0b013e328345e1f8. Review.

PMID:
21460730
18.

Pharmacokinetics and safety of MP-376 (levofloxacin inhalation solution) in cystic fibrosis subjects.

Geller DE, Flume PA, Griffith DC, Morgan E, White D, Loutit JS, Dudley MN.

Antimicrob Agents Chemother. 2011 Jun;55(6):2636-40. doi: 10.1128/AAC.01744-10. Epub 2011 Mar 28.

19.

Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: The EAGER trial.

Konstan MW, Flume PA, Kappler M, Chiron R, Higgins M, Brockhaus F, Zhang J, Angyalosi G, He E, Geller DE.

J Cyst Fibros. 2011 Jan;10(1):54-61. doi: 10.1016/j.jcf.2010.10.003. Epub 2010 Nov 12.

20.

Cystic fibrosis pulmonary guidelines: pulmonary complications: hemoptysis and pneumothorax.

Flume PA, Mogayzel PJ Jr, Robinson KA, Rosenblatt RL, Quittell L, Marshall BC; Clinical Practice Guidelines for Pulmonary Therapies Committee; Cystic Fibrosis Foundation Pulmonary Therapies Committee.

Am J Respir Crit Care Med. 2010 Aug 1;182(3):298-306. doi: 10.1164/rccm.201002-0157CI.

PMID:
20675678
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