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Journal Abstract Search

1598 related items for PubMed ID: 22047557

  • 1. A CFTR potentiator in patients with cystic fibrosis and the G551D mutation.
    Ramsey BW, Davies J, McElvaney NG, Tullis E, Bell SC, Dřevínek P, Griese M, McKone EF, Wainwright CE, Konstan MW, Moss R, Ratjen F, Sermet-Gaudelus I, Rowe SM, Dong Q, Rodriguez S, Yen K, Ordoñez C, Elborn JS, VX08-770-102 Study Group.
    N Engl J Med; 2011 Nov 03; 365(18):1663-72. PubMed ID: 22047557
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  • 2. Efficacy and safety of ivacaftor in patients aged 6 to 11 years with cystic fibrosis with a G551D mutation.
    Davies JC, Wainwright CE, Canny GJ, Chilvers MA, Howenstine MS, Munck A, Mainz JG, Rodriguez S, Li H, Yen K, Ordoñez CL, Ahrens R, VX08-770-103 (ENVISION) Study Group.
    Am J Respir Crit Care Med; 2013 Jun 01; 187(11):1219-25. PubMed ID: 23590265
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  • 3. Potentiators (specific therapies for class III and IV mutations) for cystic fibrosis.
    Skilton M, Krishan A, Patel S, Sinha IP, Southern KW.
    Cochrane Database Syst Rev; 2019 Jan 07; 1(1):CD009841. PubMed ID: 30616300
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  • 4. Potentiators (specific therapies for class III and IV mutations) for cystic fibrosis.
    Patel S, Sinha IP, Dwan K, Echevarria C, Schechter M, Southern KW.
    Cochrane Database Syst Rev; 2015 Mar 26; (3):CD009841. PubMed ID: 25811419
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  • 6. Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del.
    Taylor-Cousar JL, Munck A, McKone EF, van der Ent CK, Moeller A, Simard C, Wang LT, Ingenito EP, McKee C, Lu Y, Lekstrom-Himes J, Elborn JS.
    N Engl J Med; 2017 Nov 23; 377(21):2013-2023. PubMed ID: 29099344
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  • 8. Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial.
    Davies J, Sheridan H, Bell N, Cunningham S, Davis SD, Elborn JS, Milla CE, Starner TD, Weiner DJ, Lee PS, Ratjen F.
    Lancet Respir Med; 2013 Oct 23; 1(8):630-638. PubMed ID: 24461666
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  • 9. Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.
    Wainwright CE, Elborn JS, Ramsey BW, Marigowda G, Huang X, Cipolli M, Colombo C, Davies JC, De Boeck K, Flume PA, Konstan MW, McColley SA, McCoy K, McKone EF, Munck A, Ratjen F, Rowe SM, Waltz D, Boyle MP, TRAFFIC Study Group, TRANSPORT Study Group.
    N Engl J Med; 2015 Jul 16; 373(3):220-31. PubMed ID: 25981758
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  • 10. Elexacaftor-Tezacaftor-Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele.
    Middleton PG, Mall MA, Dřevínek P, Lands LC, McKone EF, Polineni D, Ramsey BW, Taylor-Cousar JL, Tullis E, Vermeulen F, Marigowda G, McKee CM, Moskowitz SM, Nair N, Savage J, Simard C, Tian S, Waltz D, Xuan F, Rowe SM, Jain R, VX17-445-102 Study Group.
    N Engl J Med; 2019 Nov 07; 381(19):1809-1819. PubMed ID: 31697873
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  • 11. Efficacy and safety of lumacaftor and ivacaftor in patients aged 6-11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial.
    Ratjen F, Hug C, Marigowda G, Tian S, Huang X, Stanojevic S, Milla CE, Robinson PD, Waltz D, Davies JC, VX14-809-109 investigator group.
    Lancet Respir Med; 2017 Jul 07; 5(7):557-567. PubMed ID: 28606620
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  • 14. Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trial.
    Moss RB, Flume PA, Elborn JS, Cooke J, Rowe SM, McColley SA, Rubenstein RC, Higgins M, VX11-770-110 (KONDUCT) Study Group.
    Lancet Respir Med; 2015 Jul 07; 3(7):524-33. PubMed ID: 26070913
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  • 16. Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation.
    Accurso FJ, Rowe SM, Clancy JP, Boyle MP, Dunitz JM, Durie PR, Sagel SD, Hornick DB, Konstan MW, Donaldson SH, Moss RB, Pilewski JM, Rubenstein RC, Uluer AZ, Aitken ML, Freedman SD, Rose LM, Mayer-Hamblett N, Dong Q, Zha J, Stone AJ, Olson ER, Ordoñez CL, Campbell PW, Ashlock MA, Ramsey BW.
    N Engl J Med; 2010 Nov 18; 363(21):1991-2003. PubMed ID: 21083385
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