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D Dusser

Showing results (41-50 of 85) with videos related to

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Thorax|September 1, 1990
Effects of inflammation and fibrosis on pulmonary function in diffuse lung fibrosisT Chinet, F Jaubert, D Dusser, et al.
Human Molecular Genetics|February 1, 1994
A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patientT Bienvenu, C Cazeneuve, C Beldjord, et al.
Human Mutation|January 1, 1996
A novel missense mutation in exon 16 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in CBAVD patientsT Bienvenu, D Hubert, E Setbon, et al.
Bulletin Europeen De Physiopathologie Respiratoire|May 1, 1984
[Respiratory permeability studies by clearance of an aerosol solute and bronchoalveolar lavage in interstitial pneumopathies]D Dusser, M Mordelet-Dambrine, M A Collignon, et al.
Revue Medicale De La Suisse Romande|December 1, 1991
[Asthma, allergy, current aspects. Tachykinins: clinical and therapeutic implications. Report of the 3A of 22 June 1991]B S Polla, K F Chung, J M Lundberg, et al.
The American Review of Respiratory Disease|February 1, 1990
Lung function declines in patients with pulmonary sarcoidosis and increased respiratory epithelial permeability to 99mTc-DTPAT Chinet, D Dusser, S Labrune, et al.
Therapeutic Drug Monitoring|January 1, 1986
Comparison between theophylline analysis by nephelometric inhibition immunoassay and high performance liquid chromatographyM Mordelet-Dambrine, J Y Baglin, A Roux, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 8, 2000
High susceptibility for cystic fibrosis human airway gland cells to produce IL-8 through the I kappa B kinase alpha pathway in response to extracellular NaCl contentO Tabary, S Escotte, J P Couetil, et al.
Clinical and Experimental Immunology|May 22, 2001
Quantitative analysis of inflammatory cells infiltrating the cystic fibrosis airway mucosaC Hubeau, M Lorenzato, J P Couetil, et al.
Clinical Genetics|August 16, 2003
Mutations located in exon 24 of the CFTR gene are associated with a mild cystic fibrosis phenotypeT Bienvenu, M Viel, C Leroy, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Thorax|September 1, 1990
Effects of inflammation and fibrosis on pulmonary function in diffuse lung fibrosisT Chinet, F Jaubert, D Dusser, et al.
Human Molecular Genetics|February 1, 1994
A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patientT Bienvenu, C Cazeneuve, C Beldjord, et al.
Human Mutation|January 1, 1996
A novel missense mutation in exon 16 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in CBAVD patientsT Bienvenu, D Hubert, E Setbon, et al.
Bulletin Europeen De Physiopathologie Respiratoire|May 1, 1984
[Respiratory permeability studies by clearance of an aerosol solute and bronchoalveolar lavage in interstitial pneumopathies]D Dusser, M Mordelet-Dambrine, M A Collignon, et al.
Revue Medicale De La Suisse Romande|December 1, 1991
[Asthma, allergy, current aspects. Tachykinins: clinical and therapeutic implications. Report of the 3A of 22 June 1991]B S Polla, K F Chung, J M Lundberg, et al.
The American Review of Respiratory Disease|February 1, 1990
Lung function declines in patients with pulmonary sarcoidosis and increased respiratory epithelial permeability to 99mTc-DTPAT Chinet, D Dusser, S Labrune, et al.
Therapeutic Drug Monitoring|January 1, 1986
Comparison between theophylline analysis by nephelometric inhibition immunoassay and high performance liquid chromatographyM Mordelet-Dambrine, J Y Baglin, A Roux, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 8, 2000
High susceptibility for cystic fibrosis human airway gland cells to produce IL-8 through the I kappa B kinase alpha pathway in response to extracellular NaCl contentO Tabary, S Escotte, J P Couetil, et al.
Clinical and Experimental Immunology|May 22, 2001
Quantitative analysis of inflammatory cells infiltrating the cystic fibrosis airway mucosaC Hubeau, M Lorenzato, J P Couetil, et al.
Clinical Genetics|August 16, 2003
Mutations located in exon 24 of the CFTR gene are associated with a mild cystic fibrosis phenotypeT Bienvenu, M Viel, C Leroy, et al.
Pageof 9