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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.
Respiratory Medicine
|
July 23, 2017
Heterogeneity of lung disease associated with NK2 homeobox 1 mutations
Elodie Nattes, Stephanie Lejeune, Ania Carsin, et al.
Human Molecular Genetics
|
November 10, 2011
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children
Florence 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 fibrosis
Raphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Orphanet Journal of Rare Diseases
|
April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experience
Aurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 7, 2020
Targeting p16<sup>INK4a</sup> Promotes Lipofibroblasts and Alveolar Regeneration after Early-Life Injury
Maéva Zysman, Bruno Ribeiro Baptista, Laure-Aléa Essari, et al.
Clinical Pharmacokinetics
|
February 4, 2024
Lumacaftor/Ivacaftor Population Pharmacokinetics in Pediatric Patients with Cystic Fibrosis: A First Step Toward Personalized Therapy
Naïm Bouazza, Saïk Urien, Frantz Foissac, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 27, 2012
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene
Domitille Gras, Laurence Jonard, Emmanuel Roze, et al.
Orphanet Journal of Rare Diseases
|
February 5, 2010
Retrospective French nationwide survey of childhood aggressive vascular anomalies of bone, 1988-2009
Sébastien Héritier, Martine Le Merrer, Francis Jaubert, et al.
Orphanet Journal of Rare Diseases
|
September 10, 2020
Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study
Solenne Le Louet, Mohamed-Aziz Barkaoui, Jean Miron, et al.
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Search research articles
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Showing results (91-100 of 114) with videos related to
Sort By:
Page
of 12
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.
Respiratory Medicine
|
July 23, 2017
Heterogeneity of lung disease associated with NK2 homeobox 1 mutations
Elodie Nattes, Stephanie Lejeune, Ania Carsin, et al.
Human Molecular Genetics
|
November 10, 2011
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children
Florence 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 fibrosis
Raphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Orphanet Journal of Rare Diseases
|
April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experience
Aurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 7, 2020
Targeting p16<sup>INK4a</sup> Promotes Lipofibroblasts and Alveolar Regeneration after Early-Life Injury
Maéva Zysman, Bruno Ribeiro Baptista, Laure-Aléa Essari, et al.
Clinical Pharmacokinetics
|
February 4, 2024
Lumacaftor/Ivacaftor Population Pharmacokinetics in Pediatric Patients with Cystic Fibrosis: A First Step Toward Personalized Therapy
Naïm Bouazza, Saïk Urien, Frantz Foissac, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 27, 2012
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene
Domitille Gras, Laurence Jonard, Emmanuel Roze, et al.
Orphanet Journal of Rare Diseases
|
February 5, 2010
Retrospective French nationwide survey of childhood aggressive vascular anomalies of bone, 1988-2009
Sébastien Héritier, Martine Le Merrer, Francis Jaubert, et al.
Orphanet Journal of Rare Diseases
|
September 10, 2020
Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study
Solenne Le Louet, Mohamed-Aziz Barkaoui, Jean Miron, et al.
Page
of 12