Search Results - "Epaud, Ralph"

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Knockout of Insulin-Like Growth Factor-1 Receptor Impairs Distal Lung Morphogenesis.

Authors: Epaud, Ralph Aubey, Flore Jie Xu et al.

Source: PLoS ONE. Nov2012, Vol. 7 Issue 11, Special section p1-12. 12p.

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Deficiency in type 1 insulin-like growth factor receptor in mice protects against oxygen-induced lung injury.

Authors: Ahamed, Karmene Epaud, Ralph Holzenberger, Martin et al.

Source: Respiratory Research. 2005, Vol. 6, p31-11. 11p.

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Acute exposure to realistic simulated urban atmospheres exacerbates pulmonary phenotype in cystic fibrosis-like mice.

Authors: Blayac, Marion Yegen, Céline-Hivda Marj, Elie Al et al.

Source: Journal of Hazardous Materials; Mar2024, Vol. 465, pN.PAG-N.PAG, 1p

Airway Mycobiota—Microbiota During Pulmonary Exacerbation of Cystic Fibrosis Patients: A Culture and Targeted Sequencing Study.

Authors: Angebault, Cécile Vandenborght, Louise‐Eva Bassinet, Laurence et al.

Source: Mycoses. Jan2025, Vol. 68 Issue 1, p1-13. 13p.

Multiplex Ligation-Dependent Probe Amplification Improves the Detection Rate of NKX2.1 Mutations in Patients Affected by Brain-Lung-Thyroid Syndrome.

Authors: Teissier, Raphaël Guillot, Loïc Carré, Aurore et al.

Source: Hormone Research in Paediatrics. May2012, Vol. 77 Issue 3, p146-151.

Impact of RSV hospitalization on healthcare costs, caregivers’ productivity loss, and quality of life in children ≤ 2 years old in five European countries.

Authors: Wildenbeest, Joanne G. Bont, Louis Cianci, Daniela et al.

Source: European Journal of Pediatrics. Nov2025, Vol. 184 Issue 11, p1-12. 12p.

A national internet-linked based database for pediatric interstitial lung diseases: the French network.

Authors: Nathan, Nadia Taam, Rola Abou Epaud, Ralph et al.

Source: Orphanet Journal of Rare Diseases. 2012, Vol. 7 Issue 1, p40-50. 11p. 5 Charts, 1 Graph.

Interstitial lung diseases in children.

Authors: Clement, Annick Nathan, Nadia Epaud, Ralph et al.

Source: Orphanet Journal of Rare Diseases. 2010, Vol. 5, p22-45. 24p.

Dynamics of RSV hospitalization rates in ≤ 2-year-old children between 2020–2023 in Europe.

Authors: Wildenbeest, Joanne G. Bont, Louis Cianci, Daniela et al.

Source: European Journal of Pediatrics. Oct2025, Vol. 184 Issue 10, p1-11. 11p.

Long-term evolution of neuroendocrine cell hyperplasia of infancy: the FRENCHI findings.

Authors: Dervaux, Morgane Thumerelle, Caroline Fabre, Candice et al.

Source: European Journal of Pediatrics. Feb2023, Vol. 182 Issue 2, p949-956. 8p. 2 Charts.

Tezacaftor/ivacaftor in people with cystic fibrosis who stopped lumacaftor/ivacaftor due to respiratory adverse events.

Authors: Schwarz, Carsten Sutharsan, Sivagurunathan Epaud, Ralph et al.

Source: Journal of Cystic Fibrosis. Mar2021, Vol. 20 Issue 2, p228-233. 6p.

Impact of A Multidisciplinary Team Discussion for Genetic Lung Fibrosis.

Authors: Franco, Giovanni Ba, Ibrahima Nathan, Nadia et al.

Source: Respirology. Jun2025, Vol. 30 Issue 6, p523-532. 10p.

French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial management.

Authors: Fabre, Candice Thumerelle, Caroline Dervaux, Morgane et al.

Source: European Journal of Pediatrics. Aug2022, Vol. 181 Issue 8, p3067-3073. 7p.

Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study.

Authors: Le Louet, Solenne Barkaoui, Mohamed-Aziz Miron, Jean et al.

Source: Orphanet Journal of Rare Diseases. 9/9/2020, Vol. 15 Issue 1, p1-11. 11p.

Lumacaftor/Ivacaftor Population Pharmacokinetics in Pediatric Patients with Cystic Fibrosis: A First Step Toward Personalized Therapy.

Authors: Bouazza, Naïm Urien, Saïk Foissac, Frantz et al.

Source: Clinical Pharmacokinetics. Mar2024, Vol. 63 Issue 3, p333-342. 10p.

Lung alveolar epithelium and interstitial lung disease

Authors: Corvol, Harriet Flamein, Florence Epaud, Ralph et al.

Source: International Journal of Biochemistry & Cell Biology. Aug2009, Vol. 41 Issue 8/9, p1643-1651. 9p.