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Annick Clement

Showing results (61-70 of 100) with videos related to

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ERJ Open Research|July 31, 2019
Bi-allelic missense <i>ABCA3</i> mutations in a patient with childhood ILD who reached adulthoodEffrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Hormone Research in Paediatrics|April 11, 2012
Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndromeRaphaël Teissier, Loïc Guillot, Aurore Carré, et al.
Plos One|November 10, 2012
Knockout of insulin-like growth factor-1 receptor impairs distal lung morphogenesisRalph Epaud, Flore Aubey, Jie Xu, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 14, 2011
Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patientsHarriet Corvol, Julie Beucher, Pierre-Yves Boëlle, et al.
Pharmacogenetics|April 30, 2004
Glutathione-S-transferase M1, M3, P1 and T1 polymorphisms and severity of lung disease in children with cystic fibrosisCyril Flamant, Alexandra Henrion-Caude, Pierre-Yves Boëlle, et al.
Orphanet Journal of Rare Diseases|October 16, 2013
New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(®) cohortJessica Taytard, Nadia Nathan, Jacques de Blic, et al.
Orphanet Journal of Rare Diseases|February 22, 2014
Idiopathic eosinophilic pneumonia in children: the French experienceLisa Giovannini-Chami, Alice Hadchouel, Nadia Nathan, et al.
Journal of Medical Genetics|November 28, 2019
Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesiaSylvain Blanchon, Marie Legendre, Mathieu Bottier, et al.
Archives of Disease in Childhood|April 21, 2010
Characteristics of disorders associated with genetic mutations of surfactant protein CGuillaume Thouvenin, Rola Abou Taam, Florence Flamein, et al.
Pediatric Pulmonology|November 15, 2008
Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosisHarriet Corvol, Pierre-Yves Boelle, Jacques Brouard, et al.
Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:
Pageof 10
ERJ Open Research|July 31, 2019
Bi-allelic missense <i>ABCA3</i> mutations in a patient with childhood ILD who reached adulthoodEffrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Hormone Research in Paediatrics|April 11, 2012
Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndromeRaphaël Teissier, Loïc Guillot, Aurore Carré, et al.
Plos One|November 10, 2012
Knockout of insulin-like growth factor-1 receptor impairs distal lung morphogenesisRalph Epaud, Flore Aubey, Jie Xu, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 14, 2011
Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patientsHarriet Corvol, Julie Beucher, Pierre-Yves Boëlle, et al.
Pharmacogenetics|April 30, 2004
Glutathione-S-transferase M1, M3, P1 and T1 polymorphisms and severity of lung disease in children with cystic fibrosisCyril Flamant, Alexandra Henrion-Caude, Pierre-Yves Boëlle, et al.
Orphanet Journal of Rare Diseases|October 16, 2013
New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(®) cohortJessica Taytard, Nadia Nathan, Jacques de Blic, et al.
Orphanet Journal of Rare Diseases|February 22, 2014
Idiopathic eosinophilic pneumonia in children: the French experienceLisa Giovannini-Chami, Alice Hadchouel, Nadia Nathan, et al.
Journal of Medical Genetics|November 28, 2019
Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesiaSylvain Blanchon, Marie Legendre, Mathieu Bottier, et al.
Archives of Disease in Childhood|April 21, 2010
Characteristics of disorders associated with genetic mutations of surfactant protein CGuillaume Thouvenin, Rola Abou Taam, Florence Flamein, et al.
Pediatric Pulmonology|November 15, 2008
Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosisHarriet Corvol, Pierre-Yves Boelle, Jacques Brouard, et al.
Pageof 10