Elodie Nattes
Creteil, France
Last Updated: 09/26/2026
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Found 9 publications
Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variant.
Journal: Frontiers in pediatrics
Published: June 26, 2022
Methylprednisolone pulse treatment improves ProSP-C trafficking in twins with SFTPC mutation: An isoform story?
Journal: British journal of clinical pharmacology
Published: June 30, 2020
Systematic Severe Acute Respiratory Syndrome Coronavirus 2 Screening at Hospital Admission in Children: A French Prospective Multicenter Study.
Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
Published: June 17, 2020
Delayed acute bronchiolitis in infants hospitalized for COVID-19.
Journal: Pediatric pulmonology
Published: June 14, 2020
Antibiotic strategy in pleural empyema in children: Consensus by the DELPHI method
Journal: Revue des maladies respiratoires
Published: June 18, 2019
Remission of proteinuria in multidrug-resistant idiopathic nephrotic syndrome following immunoglobulin immunoadsorption.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: June 14, 2018
Progressive Development of PTH Resistance in Patients With Inactivating Mutations on the Maternal Allele of GNAS.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 27, 2016
Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.
Journal: Respiratory medicine
Published: October 23, 2016
Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype.
Journal: European journal of human genetics : EJHG
Published: October 08, 2016
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Last Updated: 09/26/2026