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PubPharm (14)
1
Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis : A Clinical Trial
enthalten in:
American journal of respiratory and critical care medicine
| 2022
von
Nichols, D.
|
Paynter, A.
|
Heltshe, S.
| +121
CommentIn: Am J Respir Crit Care Med. 2022 Mar 1;205(5):487-489. - PMID 35073504
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2
Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND) : an open-label extension study
enthalten in:
The Lancet. Respiratory medicine
| 2021
von
Flume, P.
|
Biner, R.
|
Downey, D.
| +118
ErratumIn: Lancet Respir Med. 2021 Apr;9(4):e38. - PMID 33636124
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3
Long-term safety and efficacy of lumacaftor-ivacaftor therapy in children aged 6-11 years with cystic fibrosis homozygous for the F508del-CFTR mutation : a phase 3, open-label, extension study
enthalten in:
The Lancet. Respiratory medicine
| 2021
von
Chilvers, M.
|
Davies, J.
|
Milla, C.
| +5
ErratumIn: Lancet Respir Med. 2021 Apr;9(4):e38. - PMID 33607008
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4
Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adults
enthalten in:
Scientific reports
| 2018
von
Kim, J.
|
Farahmand, M.
|
Dunn, C.
| +5
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5
Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL) : a phase 3 single-arm study
enthalten in:
The Lancet. Respiratory medicine
| 2018
von
Rosenfeld, M.
|
Wainwright, C.
|
Higgins, M.
| +38
CommentIn: Lancet Respir Med. 2018 Jul;6(7):483-484. - PMID 29886025
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6
Ivacaftor restores CFTR-dependent sweat gland fluid secretion in cystic fibrosis subjects with S945L alleles
enthalten in:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
| 2018
von
Kim, J.
|
Davies, Z.
|
Dunn, C.
| +2
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7
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
enthalten in:
The Lancet. Respiratory medicine
| 2017
von
Ratjen, F.
|
Hug, C.
|
Marigowda, G.
| +62
CommentIn: Lancet Respir Med. 2017 Jul;5(7):536-537. - PMID 28606619
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8
Lumacaftor/Ivacaftor in Patients Aged 6-11 Years with Cystic Fibrosis and Homozygous for F508del-CFTR
enthalten in:
American journal of respiratory and critical care medicine
| 2017
von
Milla, C.
|
Ratjen, F.
|
Marigowda, G.
| +4
CommentIn: Am J Respir Crit Care Med. 2017 Apr 1;195(7):849-850. - PMID 28362199
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9
The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels : Human in vivo measurements
enthalten in:
PloS one
| 2017
von
Char, J.
|
Dunn, C.
|
Davies, Z.
| +3
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10
Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis
enthalten in:
American journal of respiratory and critical care medicine
| 2014
von
Rowe, S.
|
Heltshe, S.
|
Gonska, T.
| +52
CommentIn: Am J Respir Crit Care Med. 2014 Jul 15;190(2):128-9. - PMID 25025350
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1
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Thema: Quinolones
Medienart
14
Aufsätze
14
E-Artikel
14
E-Ressourcen
Zeitschriftentitel
5
The Lancet. Respiratory medicine
3
American journal of respiratory and critical ca...
2
PloS one
1
Current opinion in pediatrics
1
JAMA
1
Journal of cystic fibrosis : official journal o...
1
Scientific reports
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Thema
14
Aminophenols
14
Journal Article
Quinolones
13
126880-72-6
13
Cystic Fibrosis Transmembrane Conductance Regul...
12
1Y740ILL1Z
12
ivacaftor
11
Research Support, Non-U.S. Gov't
6
Benzodioxoles
6
Chloride Channel Agonists
6
Multicenter Study
4
CFTR protein, human
4
Clinical Trial, Phase III
4
Drug Combinations
3
Aminopyridines
3
Indoles
2
Chlorides
2
EGP8L81APK
2
Observational Study
2
Randomized Controlled Trial
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Erscheinungszeitraum
3
2020-
11
2010-2019
Erscheinungsjahr(e)
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Sprache
14
Englisch
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