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Annick Clement

Showing results (81-90 of 100) with videos related to

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American Journal of Human Genetics|June 16, 2015
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial SpokesLudovic Jeanson, Bruno Copin, Jean-François Papon, et al.
Thorax|November 22, 2019
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD)Steve Cunningham, Catriona Graham, Morag MacLean, et al.
Human Molecular Genetics|November 10, 2011
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in childrenFlorence Flamein, Laure Riffault, Céline Muselet-Charlier, et al.
Orphanet Journal of Rare Diseases|December 5, 2019
Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosisRaphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Orphanet Journal of Rare Diseases|April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experienceAurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
Human Molecular Genetics|January 22, 2016
Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancerNadia Nathan, Violaine Giraud, Clément Picard, et al.
Pediatric Pulmonology|March 15, 2019
Health-related quality of life in infants and children with interstitial lung diseaseClara Lauby, Pierre-Yves Boelle, Rola Abou Taam, et al.
The European Respiratory Journal|January 6, 2017
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first resultsMyrofora Goutaki, Elisabeth Maurer, Florian S Halbeisen, et al.
American Journal of Human Genetics|September 3, 2013
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defectsEsther Kott, Marie Legendre, Bruno Copin, et al.
Orphanet Journal of Rare Diseases|June 19, 2012
A national internet-linked based database for pediatric interstitial lung diseases: the French networkNadia Nathan, Rola Abou Taam, Ralph Epaud, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|June 16, 2015
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial SpokesLudovic Jeanson, Bruno Copin, Jean-François Papon, et al.
Thorax|November 22, 2019
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD)Steve Cunningham, Catriona Graham, Morag MacLean, et al.
Human Molecular Genetics|November 10, 2011
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in childrenFlorence Flamein, Laure Riffault, Céline Muselet-Charlier, et al.
Orphanet Journal of Rare Diseases|December 5, 2019
Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosisRaphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Orphanet Journal of Rare Diseases|April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experienceAurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
Human Molecular Genetics|January 22, 2016
Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancerNadia Nathan, Violaine Giraud, Clément Picard, et al.
Pediatric Pulmonology|March 15, 2019
Health-related quality of life in infants and children with interstitial lung diseaseClara Lauby, Pierre-Yves Boelle, Rola Abou Taam, et al.
The European Respiratory Journal|January 6, 2017
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first resultsMyrofora Goutaki, Elisabeth Maurer, Florian S Halbeisen, et al.
American Journal of Human Genetics|September 3, 2013
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defectsEsther Kott, Marie Legendre, Bruno Copin, et al.
Orphanet Journal of Rare Diseases|June 19, 2012
A national internet-linked based database for pediatric interstitial lung diseases: the French networkNadia Nathan, Rola Abou Taam, Ralph Epaud, et al.
Pageof 10