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pro vyhledávání: '"Iram Haq"'
Autor:
Mollestad, Marthe Bratseth
Masteroppgave i nordisk litteratur Institutt for lingvistiske, litterære og estetiske studium Universitetet i Bergen, Våren 2021 Student: Marthe Mollestad Tittel: Migrasjonslitteratur i klasserommet Undertittel: En kvalitativ studie av en gruppe un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::de9f0bc874b10ad6e66667a8b058b2d4
https://hdl.handle.net/11250/2761209
https://hdl.handle.net/11250/2761209
Publikováno v:
BMJ Open Respiratory Research, Vol 11, Iss 1 (2024)
Background Pulmonary exacerbations (PExs) are clinically important in people with cystic fibrosis (CF). Multiple definitions have been used for PEx, and this scoping review aimed to identify the different definitions reported in the literature and to
Externí odkaz:
https://doaj.org/article/9653956dcfff48b78201a5d9c4baf5b7
Autor:
Anette Svane
Publikováno v:
Women in the International Film Industry ISBN: 9783030390693
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c6a48e4fb92fc10a2acb119088d257e
https://doi.org/10.1007/978-3-030-39070-9_9
https://doi.org/10.1007/978-3-030-39070-9_9
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Publikováno v:
BMJ Open Respiratory Research, Vol 10, Iss Suppl 1 (2023)
Externí odkaz:
https://doaj.org/article/225819d196a742b98b7c4ff07207759b
Publikováno v:
BMJ Open Respiratory Research, Vol 9, Iss 1 (2022)
Background Cystic fibrosis (CF) is a genetic condition caused by variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that primarily impacts the lungs. Treatments historically have been symptomatic to improve airway clearan
Externí odkaz:
https://doaj.org/article/53326c826c7d4bb8a2501a5f37624e91
Autor:
Dancus, Adriana Margareta1 (AUTHOR) Adriana.M.Dancus@usn.no
Publikováno v:
NORA: Nordic Journal of Women's Studies. Jun2023, Vol. 31 Issue 2, p128-138. 11p.
Autor:
Maryam Almulhem, Nuala Harnett, Stephanie Graham, Iram Haq, Shelina Visram, Christopher Ward, Malcolm Brodlie
Publikováno v:
BMJ open respiratory research. 9(1)
BackgroundCystic fibrosis (CF) is a genetic condition caused by variants in thecystic fibrosis transmembrane conductance regulator (CFTR) gene that primarily impacts the lungs. Treatments historically have been symptomatic to improve airway clearance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a56aba68c8b4772d3a39dba3819e0cc
https://pubmed.ncbi.nlm.nih.gov/36207030
https://pubmed.ncbi.nlm.nih.gov/36207030