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American Journal of Respiratory and Critical Care Medicine
|
April 10, 2025
Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Adults and Adolescents with Cystic Fibrosis and at Least One <i>F508del</i> Allele: A Phase 3, Open-Label Extension Study
Cori L Daines, Deepika Polineni, Elizabeth Tullis, et al.
Clinical and Experimental Pediatrics
|
June 19, 2026
Telomere biology disorders associated with childhood interstitial lung disease
Maria Greiner-Mai, Christina Katharina Rapp, Katrin Knoflach, et al.
The American Journal of Pathology
|
November 29, 2023
Multilamellated Basement Membranes in the Capillary Network of Alveolar Capillary Dysplasia
Jan C Kamp, Lavinia Neubert, Jonas C Schupp, et al.
The European Respiratory Journal
|
November 9, 2023
Long-term safety and efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis and at least one <i>F508del</i> allele: 144-week interim results from a 192-week open-label extension study
Cori L Daines, Elizabeth Tullis, Stefano Costa, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 4, 2024
Genetics and Genomics of Pulmonary Fibrosis: Charting the Molecular Landscape and Shaping Precision Medicine
Ayodeji Adegunsoye, Jonathan A Kropski, Juergen Behr, et al.
The European Respiratory Journal
|
June 21, 2022
European Respiratory Society statement for defining respiratory exacerbations in children and adolescents with bronchiectasis for clinical trials
Anne B Chang, Angela Zacharasiewicz, Vikas Goyal, et al.
Nature Genetics
|
April 22, 2014
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia
Julia Wallmeier, Dalal A Al-Mutairi, Chun-Ting Chen, et al.
Journal of Medical Genetics
|
April 10, 2014
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum
Anne Thorwarth, Sarah Schnittert-Hübener, Pamela Schrumpf, et al.
Ebiomedicine
|
March 1, 2025
Bi-allelic LAMP3 variants in childhood interstitial lung disease: a surfactant-related disease
Camille Louvrier, Tifenn Desroziers, Yohan Soreze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 7, 2026
Biallelic LAMP3 Variants in Five Families with Interstitial Lung Disease: Evidence of a Disease-Gene Association
Laura A Keehan, Hitomi Ono-Minagi, Mohamad Hadhud, et al.
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of 28
Search research articles
Search
Showing results (251-260 of 280) with videos related to
Sort By:
Page
of 28
American Journal of Respiratory and Critical Care Medicine
|
April 10, 2025
Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Adults and Adolescents with Cystic Fibrosis and at Least One <i>F508del</i> Allele: A Phase 3, Open-Label Extension Study
Cori L Daines, Deepika Polineni, Elizabeth Tullis, et al.
Clinical and Experimental Pediatrics
|
June 19, 2026
Telomere biology disorders associated with childhood interstitial lung disease
Maria Greiner-Mai, Christina Katharina Rapp, Katrin Knoflach, et al.
The American Journal of Pathology
|
November 29, 2023
Multilamellated Basement Membranes in the Capillary Network of Alveolar Capillary Dysplasia
Jan C Kamp, Lavinia Neubert, Jonas C Schupp, et al.
The European Respiratory Journal
|
November 9, 2023
Long-term safety and efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis and at least one <i>F508del</i> allele: 144-week interim results from a 192-week open-label extension study
Cori L Daines, Elizabeth Tullis, Stefano Costa, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 4, 2024
Genetics and Genomics of Pulmonary Fibrosis: Charting the Molecular Landscape and Shaping Precision Medicine
Ayodeji Adegunsoye, Jonathan A Kropski, Juergen Behr, et al.
The European Respiratory Journal
|
June 21, 2022
European Respiratory Society statement for defining respiratory exacerbations in children and adolescents with bronchiectasis for clinical trials
Anne B Chang, Angela Zacharasiewicz, Vikas Goyal, et al.
Nature Genetics
|
April 22, 2014
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia
Julia Wallmeier, Dalal A Al-Mutairi, Chun-Ting Chen, et al.
Journal of Medical Genetics
|
April 10, 2014
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum
Anne Thorwarth, Sarah Schnittert-Hübener, Pamela Schrumpf, et al.
Ebiomedicine
|
March 1, 2025
Bi-allelic LAMP3 variants in childhood interstitial lung disease: a surfactant-related disease
Camille Louvrier, Tifenn Desroziers, Yohan Soreze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 7, 2026
Biallelic LAMP3 Variants in Five Families with Interstitial Lung Disease: Evidence of a Disease-Gene Association
Laura A Keehan, Hitomi Ono-Minagi, Mohamad Hadhud, et al.
Page
of 28