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  1. Book: Kendig's Disorders of the Respiratory Tract in Children

    Li, Albert / Bush, Andrew / Ratjen, Felix / Zar, Heather / Sly, Peter / Wilmott, Robert W. / Deterding, Robin R

    2018  

    Author's details Peter Sly, MD is Director, Children's Health and Environment Program and Director, WHO Collaborating Centre for Children's Health and Environment. Centre for Child Health Research, South Brisbane, Australia
    Keywords Praxisbuch ; MHMC120 ; MHMC080
    Language English
    Size 1232 p.
    Edition 9
    Publisher Elsevier - Health Sciences Division
    Document type Book
    Note PDA Manuell_10
    Format 222 x 284 x 48
    ISBN 9780323448871 ; 0323448879
    Database PDA

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  2. Article ; Online: Re: Impact of spiroware re-analysis method on multiple-breath washout outcomes in children with cystic fibrosis; M.A. Oestreich, F. Wyler, P. Latzin et al.

    Jensen, Renee / Shaw, Michelle / Phanthanourak, Angel / Ratjen, Felix

    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

    2022  Volume 21, Issue 3, Page(s) e210–e211

    MeSH term(s) Breath Tests/methods ; Child ; Cystic Fibrosis/diagnosis ; Functional Residual Capacity ; Humans ; Lung ; Respiratory Function Tests
    Language English
    Publishing date 2022-04-09
    Publishing country Netherlands
    Document type Letter ; Comment
    ZDB-ID 2084724-5
    ISSN 1873-5010 ; 1569-1993
    ISSN (online) 1873-5010
    ISSN 1569-1993
    DOI 10.1016/j.jcf.2022.04.001
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  3. Article ; Online: Are we there yet? The ongoing journey of cystic fibrosis care.

    Perrem, Lucy / Ratjen, Felix

    Lancet (London, England)

    2023  Volume 402, Issue 10408, Page(s) 1113–1115

    Language English
    Publishing date 2023-09-09
    Publishing country England
    Document type Journal Article
    ZDB-ID 3306-6
    ISSN 1474-547X ; 0023-7507 ; 0140-6736
    ISSN (online) 1474-547X
    ISSN 0023-7507 ; 0140-6736
    DOI 10.1016/S0140-6736(23)01727-0
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  4. Article: Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass.

    Mouzaki, Marialena / Dupuis, Annie / Avolio, Julie / Griffin, Katherine / Ratjen, Felix / Tullis, Elizabeth / Gonska, Tanja

    Frontiers in pharmacology

    2023  Volume 14, Page(s) 1157459

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2023-07-13
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587355-6
    ISSN 1663-9812
    ISSN 1663-9812
    DOI 10.3389/fphar.2023.1157459
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  5. Article ; Online: Cystic Fibrosis.

    Grasemann, Hartmut / Ratjen, Felix

    The New England journal of medicine

    2023  Volume 389, Issue 18, Page(s) 1693–1707

    MeSH term(s) Humans ; Cystic Fibrosis/complications ; Cystic Fibrosis/diagnosis ; Cystic Fibrosis/genetics ; Cystic Fibrosis/therapy ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics
    Chemical Substances Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6)
    Language English
    Publishing date 2023-11-01
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMra2216474
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  6. Article ; Online: A new triple combination cystic fibrosis transmembrane regulator modulator.

    Perrem, Lucy / Ratjen, Felix

    The Lancet. Respiratory medicine

    2023  Volume 11, Issue 6, Page(s) 499–500

    MeSH term(s) Humans ; Cystic Fibrosis/drug therapy ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics ; Aminopyridines/therapeutic use ; Mutation ; Aminophenols/therapeutic use ; Benzodioxoles/therapeutic use
    Chemical Substances Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6) ; Aminopyridines ; Aminophenols ; Benzodioxoles
    Language English
    Publishing date 2023-02-23
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 2686754-0
    ISSN 2213-2619 ; 2213-2600
    ISSN (online) 2213-2619
    ISSN 2213-2600
    DOI 10.1016/S2213-2600(23)00001-2
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  7. Article ; Online: Charting the path to expanded access for CFTR modulator drugs: the nose knows.

    Bear, Christine / Ratjen, Felix

    The European respiratory journal

    2023  Volume 62, Issue 4

    MeSH term(s) Humans ; Cystic Fibrosis/drug therapy ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics
    Chemical Substances Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6) ; elexacaftor (RRN67GMB0V) ; ivacaftor (1Y740ILL1Z) ; tezacaftor ; CFTR protein, human
    Language English
    Publishing date 2023-10-19
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 639359-7
    ISSN 1399-3003 ; 0903-1936
    ISSN (online) 1399-3003
    ISSN 0903-1936
    DOI 10.1183/13993003.01387-2023
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    Zs.MO 292: Show issues

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  8. Book: Aerosol therapies in cystic fibrosis

    Ratjen, Felix

    (Pediatric pulmonology ; 43,9, Suppl. A)

    2008  

    Author's details Felix Ratjen, ed
    Series title Pediatric pulmonology ; 43,9, Suppl. A
    Collection
    Language English
    Size S36 S. : Ill., graph. Darst.
    Publisher Wiley-Liss
    Publishing place Hoboken, NJ
    Publishing country United States
    Document type Book
    HBZ-ID HT015690344
    Database Catalogue ZB MED Medicine, Health

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    Shelf markLoan statusLocation
    Zs A 2143 -43,Suppl.A- not available for loan Zeitschriften-Lesesaal

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  9. Article ; Online: The effect of antibiotic changes during treatment of cystic fibrosis pulmonary exacerbations.

    Zikic, Andrew / Ratjen, Felix / Shaw, Michelle / Tullis, Elizabeth / Waters, Valerie

    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

    2022  Volume 21, Issue 5, Page(s) 759–765

    Abstract: Background: Antibiotics are often changed during treatment of pulmonary exacerbations (PEx) in people with cystic fibrosis (CF) who have a poor clinical response. We aimed to characterize the reasons CF providers change antibiotics and examined the ... ...

    Abstract Background: Antibiotics are often changed during treatment of pulmonary exacerbations (PEx) in people with cystic fibrosis (CF) who have a poor clinical response. We aimed to characterize the reasons CF providers change antibiotics and examined the effects of antibiotic changes on lung function recovery.
    Methods: This was a retrospective cohort study using the Toronto CF Database from 2009 to 2015 of adults and children with CF PEx treated with intravenous antibiotics. The co-primary outcome measure was absolute and relative change in forced expiratory lung volume in 1 s (FEV
    Results: A total of 399 PEx were included of which 105 had antibiotic changes. Reasons for antibiotic changes included change in antibiotic route prior to discharge (26%), drug reactions (20%), poor FEV
    Conclusions: Changing antibiotics during CF PEx treatment in those with poor clinical response was not associated with any improved FEV
    MeSH term(s) Adult ; Anti-Bacterial Agents ; Child ; Cystic Fibrosis/complications ; Cystic Fibrosis/diagnosis ; Cystic Fibrosis/drug therapy ; Disease Progression ; Forced Expiratory Volume ; Humans ; Retrospective Studies
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2022-05-30
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2084724-5
    ISSN 1873-5010 ; 1569-1993
    ISSN (online) 1873-5010
    ISSN 1569-1993
    DOI 10.1016/j.jcf.2022.05.010
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  10. Article ; Online: Preventing Continuous Damage in Primary Ciliary Dyskinesia: Is Airway Inflammation a Potential Target?

    Gatt, Dvir / Ratjen, Felix

    Annals of the American Thoracic Society

    2022  Volume 20, Issue 1, Page(s) 26–27

    MeSH term(s) Humans ; Child ; Respiratory System ; Kartagener Syndrome ; Inflammation
    Language English
    Publishing date 2022-12-27
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 2717461-X
    ISSN 2325-6621 ; 1943-5665 ; 2325-6621
    ISSN (online) 2325-6621 ; 1943-5665
    ISSN 2325-6621
    DOI 10.1513/AnnalsATS.202209-782ED
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