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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 Disorganization
Ludovic 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 fibrosis
Pierre-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 fibrosis
Jacques 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 dyskinesia
Esther Kott, Philippe Duquesnoy, Bruno Copin, et al.
Thorax
|
November 1, 2019
Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhage
Marie-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 Cohort
Vincent 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 findings
Morgane 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 management
Candice Fabre, Caroline Thumerelle, Morgane Dervaux, et al.
BMC Medical Genomics
|
March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis
Alain 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 disease
Robin Deterding, Matthias Griese, Gail Deutsch, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 100) with videos related to
Sort By:
Page
of 10
Human Mutation
|
April 28, 2016
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization
Ludovic 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 fibrosis
Pierre-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 fibrosis
Jacques 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 dyskinesia
Esther Kott, Philippe Duquesnoy, Bruno Copin, et al.
Thorax
|
November 1, 2019
Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhage
Marie-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 Cohort
Vincent 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 findings
Morgane 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 management
Candice Fabre, Caroline Thumerelle, Morgane Dervaux, et al.
BMC Medical Genomics
|
March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis
Alain 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 disease
Robin Deterding, Matthias Griese, Gail Deutsch, et al.
Page
of 10