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Annick Clement

Showing results (71-80 of 100) with videos related to

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Human Mutation|April 28, 2016
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal DisorganizationLudovic Jeanson, Lucie Thomas, Bruno Copin, et al.
Orphanet Journal of Rare Diseases|September 11, 2012
Reference percentiles for FEV(1) and BMI in European children and adults with cystic fibrosisPierre-Yves Boëlle, Laura Viviani, Pierre-Francois Busson, et al.
The Journal of Infectious Diseases|May 5, 2005
Influence of interleukin-10 on Aspergillus fumigatus infection in patients with cystic fibrosisJacques Brouard, Nicola Knauer, Pierre-Yves Boelle, et al.
American Journal of Human Genetics|November 6, 2012
Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesiaEsther Kott, Philippe Duquesnoy, Bruno Copin, et al.
Thorax|November 1, 2019
Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhageMarie-Louise Frémond, Marie Legendre, Michael Fayon, et al.
Respiration; International Review of Thoracic Diseases|September 13, 2021
Impact of Gender on the Characteristics of Patients with Idiopathic Pulmonary Fibrosis Included in the RaDiCo-ILD CohortVincent Cottin, Sonia Gueguen, Stéphane Jouneau, et al.
European Journal of Pediatrics|November 30, 2022
Long-term evolution of neuroendocrine cell hyperplasia of infancy: the FRENCHI findingsMorgane Dervaux, Caroline Thumerelle, Candice Fabre, et al.
European Journal of Pediatrics|June 9, 2022
French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial managementCandice Fabre, Caroline Thumerelle, Morgane Dervaux, et al.
BMC Medical Genomics|March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosisAlain Calender, Pierre Antoine Rollat Farnier, Adrien Buisson, et al.
ERJ Open Research|June 24, 2021
Study design of a randomised, placebo-controlled trial of nintedanib in children and adolescents with fibrosing interstitial lung diseaseRobin Deterding, Matthias Griese, Gail Deutsch, et al.
Pageof 10

Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
Human Mutation|April 28, 2016
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal DisorganizationLudovic Jeanson, Lucie Thomas, Bruno Copin, et al.
Orphanet Journal of Rare Diseases|September 11, 2012
Reference percentiles for FEV(1) and BMI in European children and adults with cystic fibrosisPierre-Yves Boëlle, Laura Viviani, Pierre-Francois Busson, et al.
The Journal of Infectious Diseases|May 5, 2005
Influence of interleukin-10 on Aspergillus fumigatus infection in patients with cystic fibrosisJacques Brouard, Nicola Knauer, Pierre-Yves Boelle, et al.
American Journal of Human Genetics|November 6, 2012
Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesiaEsther Kott, Philippe Duquesnoy, Bruno Copin, et al.
Thorax|November 1, 2019
Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhageMarie-Louise Frémond, Marie Legendre, Michael Fayon, et al.
Respiration; International Review of Thoracic Diseases|September 13, 2021
Impact of Gender on the Characteristics of Patients with Idiopathic Pulmonary Fibrosis Included in the RaDiCo-ILD CohortVincent Cottin, Sonia Gueguen, Stéphane Jouneau, et al.
European Journal of Pediatrics|November 30, 2022
Long-term evolution of neuroendocrine cell hyperplasia of infancy: the FRENCHI findingsMorgane Dervaux, Caroline Thumerelle, Candice Fabre, et al.
European Journal of Pediatrics|June 9, 2022
French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial managementCandice Fabre, Caroline Thumerelle, Morgane Dervaux, et al.
BMC Medical Genomics|March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosisAlain Calender, Pierre Antoine Rollat Farnier, Adrien Buisson, et al.
ERJ Open Research|June 24, 2021
Study design of a randomised, placebo-controlled trial of nintedanib in children and adolescents with fibrosing interstitial lung diseaseRobin Deterding, Matthias Griese, Gail Deutsch, et al.
Pageof 10