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Journal of Clinical Medicine
|
July 2, 2020
Activated L-Arginine/Nitric Oxide Pathway in Pediatric Cystic Fibrosis and Its Association with Pancreatic Insufficiency, Liver Involvement and Nourishment: An Overview and New Results
Folke Brinkmann, Beatrice Hanusch, Manfred Ballmann, et al.
Bioconjugate Chemistry
|
November 1, 2011
Functional fluorescently labeled bithiazole ΔF508-CFTR corrector imaged in whole body slices in mice
Holly R Davison, Stephanie Taylor, Chris Drake, et al.
Journal of Clinical Medicine
|
December 1, 2020
Local and Systemic Alterations of the L-Arginine/Nitric Oxide Pathway in Sputum, Blood, and Urine of Pediatric Cystic Fibrosis Patients and Effects of Antibiotic Treatment
Beatrice Hanusch, Folke Brinkmann, Sebene Mayorandan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 24, 2019
Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism
Bente L Aalbers, Yasmin Yaakov, Nico Derichs, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 12, 2013
Nasal potential difference measurements in diagnosis of cystic fibrosis: an international survey
Lutz Naehrlich, Manfred Ballmann, Jane Davies, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 1, 2019
GLPG1837, a CFTR potentiator, in p.Gly551Asp (G551D)-CF patients: An open-label, single-arm, phase 2a study (SAPHIRA1)
Jane C Davies, Olivier Van de Steen, Silke van Koningsbruggen-Rietschel, et al.
The Journal of Pediatrics
|
January 29, 2017
Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation
Philip M Farrell, Terry B White, Clement L Ren, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 22, 2021
Riociguat for the treatment of Phe508del homozygous adults with cystic fibrosis
Nico Derichs, Jennifer L Taylor-Cousar, Jane C Davies, et al.
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of 2
Search research articles
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Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Journal of Clinical Medicine
|
July 2, 2020
Activated L-Arginine/Nitric Oxide Pathway in Pediatric Cystic Fibrosis and Its Association with Pancreatic Insufficiency, Liver Involvement and Nourishment: An Overview and New Results
Folke Brinkmann, Beatrice Hanusch, Manfred Ballmann, et al.
Bioconjugate Chemistry
|
November 1, 2011
Functional fluorescently labeled bithiazole ΔF508-CFTR corrector imaged in whole body slices in mice
Holly R Davison, Stephanie Taylor, Chris Drake, et al.
Journal of Clinical Medicine
|
December 1, 2020
Local and Systemic Alterations of the L-Arginine/Nitric Oxide Pathway in Sputum, Blood, and Urine of Pediatric Cystic Fibrosis Patients and Effects of Antibiotic Treatment
Beatrice Hanusch, Folke Brinkmann, Sebene Mayorandan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 24, 2019
Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism
Bente L Aalbers, Yasmin Yaakov, Nico Derichs, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 12, 2013
Nasal potential difference measurements in diagnosis of cystic fibrosis: an international survey
Lutz Naehrlich, Manfred Ballmann, Jane Davies, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 1, 2019
GLPG1837, a CFTR potentiator, in p.Gly551Asp (G551D)-CF patients: An open-label, single-arm, phase 2a study (SAPHIRA1)
Jane C Davies, Olivier Van de Steen, Silke van Koningsbruggen-Rietschel, et al.
The Journal of Pediatrics
|
January 29, 2017
Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation
Philip M Farrell, Terry B White, Clement L Ren, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 22, 2021
Riociguat for the treatment of Phe508del homozygous adults with cystic fibrosis
Nico Derichs, Jennifer L Taylor-Cousar, Jane C Davies, et al.
Page
of 2