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topic_facet:"Multicenter Study"
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PubPharm (23)
1
Airway Disease in Children with Primary Ciliary Dyskinesia : Impact of Ciliary Ultrastructure Defect and Genotype
enthalten in:
Annals of the American Thoracic Society
| 2023
von
Kinghorn, B.
|
Rosenfeld, M.
|
Sullivan, E.
| +15
CommentIn: Ann Am Thorac Soc. 2023 Apr;20(4):514-515. - PMID 37000147
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2
Laterality Defects in Primary Ciliary Dyskinesia : Relationship to Ultrastructural Defect or Genotype
enthalten in:
Annals of the American Thoracic Society
| 2023
von
Barber, A.
|
Shapiro, A.
|
Davis, S.
| +14
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3
Association of Neonatal Hospital Length of Stay with Lung Function in Primary Ciliary Dyskinesia
enthalten in:
Annals of the American Thoracic Society
| 2022
von
Wee, W.
|
Leigh, M.
|
Davis, S.
| +10
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4
Clinical use of shear-wave elastography for detecting liver fibrosis in children and adolescents with cystic fibrosis
enthalten in:
Pediatric radiology
| 2021
von
Levitte, S.
|
Lee, L.
|
Isaacson, J.
| +4
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5
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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6
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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7
Inhaled hypertonic saline in preschool children with cystic fibrosis (SHIP) : a multicentre, randomised, double-blind, placebo-controlled trial
enthalten in:
The Lancet. Respiratory medicine
| 2019
von
Ratjen, F.
|
Davis, S.
|
Stanojevic, S.
| +93
CommentIn: Lancet Respir Med. 2019 Sep;7(9):730-732. - PMID 31178424
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8
Primary Ciliary Dyskinesia : Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype
enthalten in:
American journal of respiratory and critical care medicine
| 2019
von
Davis, S.
|
Rosenfeld, M.
|
Lee, H.
| +12
CommentIn: Am J Respir Crit Care Med. 2019 Jan 15;199(2):136-138. - PMID 30110178
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9
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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10
Home Monitoring of Patients with Cystic Fibrosis to Identify and Treat Acute Pulmonary Exacerbations. eICE Study Results
enthalten in:
American journal of respiratory and critical care medicine
| 2017
von
Lechtzin, N.
|
Mayer-Hamblett, N.
|
West, N.
| +38
CommentIn: Am J Respir Crit Care Med. 2017 Nov 1;196 (9):1090-1092. - PMID 28696781
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Thema: Multicenter Study
Medienart
23
Aufsätze
21
E-Artikel
21
E-Ressourcen
2
Gedruckte Aufsätze
Zeitschriftentitel
6
The Lancet. Respiratory medicine
4
American journal of respiratory and critical ca...
4
Annals of the American Thoracic Society
2
Chest
2
Journal of cystic fibrosis : official journal o...
1
JAMA
1
Journal of clinical gastroenterology
1
Pediatric pulmonology
1
Pediatric radiology
1
Pediatrics
Alle anzeigen ...
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Thema
23
Journal Article
Multicenter Study
15
Research Support, Non-U.S. Gov't
12
Research Support, N.I.H., Extramural
8
Randomized Controlled Trial
7
126880-72-6
7
Cystic Fibrosis Transmembrane Conductance Regul...
6
Aminophenols
6
Quinolones
4
1Y740ILL1Z
4
Comparative Study
4
Observational Study
4
ivacaftor
3
Benzodioxoles
3
Biomarkers
3
CFTR protein, human
3
Clinical Trial, Phase II
3
Clinical Trial, Phase III
3
Drug Combinations
3
Research Support, N.I.H., Intramural
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Erscheinungszeitraum
6
2020-
14
2010-2019
3
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
23
Englisch
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