N. Nathan

发表

Surfactant protein A: A key player in lung homeostasis.

S. Amselem, A. Clément, P. Duquesnoy, 2016, The international journal of biochemistry & cell biology.

Nonsteroidal Anti-Inflammatory Drug without Antibiotics for Acute Viral Infection Increases the Empyema Risk in Children: A Matched Case-Control Study

C. Delacourt, P. Reix, I. Pin, 2016, The Journal of Pediatrics.

Interstitial lung diseases in the neonatal period

M. Legendre, N. Nathan, Yohan Sorèze, 2021 .

Eosinophilic pneumonias in children: A review of the epidemiology, diagnosis, and treatment

A. Baruchel, A. Clément, J. Dubus, 2016, Pediatric pulmonology.

Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosis

P. Dieudé, A. Cazes, S. Amselem, 2019, Orphanet Journal of Rare Diseases.

Genetic causes and clinical management of pediatric interstitial lung diseases

K. Borensztajn, A. Clément, N. Nathan, 2018, Current opinion in pulmonary medicine.

Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.

R. Epaud, R. Borie, E. Bosdure, 2017, Respiratory medicine.

Endobronchial avium mycobacteria infection in an immunocompetent child

H. Corvol, N. Nathan, B. Thierry, 2013, BMJ Case Reports.

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

C. Delacourt, P. Reix, R. Epaud, 2022, European Journal of Pediatrics.

Diffuse Parenchymal Lung Disease in Early Childhood

N. Nathan, C. Sileo, Blandine Prévost, 2021 .

Interstitial lung diseases in children.

A. Clément, N. Nathan, C. Sileo, 2020, Presse medicale.

Chronic interstitial lung diseases in children: diagnosis approaches

K. Borensztajn, A. Clément, N. Nathan, 2018, Expert review of respiratory medicine.

Inborn Errors of Metabolism: The Achilles' Heel of the Respiratory System

J. Bernaudin, D. Valeyre, N. Nathan, 2017, Respiration.

Child–Adult Transition in Sarcoidosis: A Series of 52 Patients

C. Delacourt, J. Bernaudin, R. Epaud, 2020, Journal of clinical medicine.

Paediatric sarcoidosis.

A. Clément, A. Calender, D. Valeyre, 2019, Paediatric respiratory reviews.

Genotype-Phenotype Relationships in Inheritable Idiopathic Pulmonary Fibrosis: A Greek National Cohort Study

Z. Daniil, M. Maniati, P. Revy, 2022, Respiration.

New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(R) cohort

P. Reix, R. Epaud, A. Clément, 2018 .

New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare® cohort

P. Reix, R. Epaud, A. Clément, 2013, Orphanet Journal of Rare Diseases.

Alveolar epithelial cells: master regulators of lung homeostasis.

L. Guillot, S. Amselem, A. Clément, 2013, The international journal of biochemistry & cell biology.

SARS-CoV-2 B.1.1.529 (Omicron) Variant Causes an Unprecedented Surge in Children Hospitalizations and Distinct Clinical Presentation Compared to the SARS-CoV-2 B.1.617.2 (Delta) Variant

G. Thouvenin, H. Corvol, N. Nathan, 2022, Frontiers in Pediatrics.

COPA syndrome, 5 years after: where are we?

M. Frémond, N. Nathan, 2020, Joint bone spine.

Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhage

Y. Crow, S. Amselem, D. Duffy, 2019, Thorax.

Comparison of comorbidities between rheumatoid and psoriatic arthritis in a tertiary care rheumatic center

N. Nathan, T. Selvam, V. Sowndhariya, 2018 .

Benefits and risks of bronchoalveolar lavage in severe asthma in children

H. Corvol, N. Nathan, J. Taytard, 2021, ERJ Open Research.

Pulmonary hemosiderosis in children with Down syndrome: a national experience

P. Reix, R. Epaud, A. Clément, 2018, Orphanet Journal of Rare Diseases.

Bi-allelic missense ABCA3 mutations in a patient with childhood ILD who reached adulthood

S. Amselem, A. Clément, R. Borie, 2019, ERJ Open Research.

Lung sarcoidosis in children: update on disease expression and management

R. Epaud, A. Clément, P. Busson, 2015, Thorax.

Dramatic improvement after tocilizumab of severe COVID‐19 in a child with sickle cell disease and acute chest syndrome

H. Ducou le Pointe, H. Corvol, N. Nathan, 2020, American journal of hematology.

Chronic eosinophilic pneumonia in a 13-year-old child

R. Epaud, A. Clément, S. Blanchon, 2008, European Journal of Pediatrics.

[Bronchopulmonary dysplasia-associated pulmonary arterial hypertension of very preterm infants].

R. Epaud, S. Essouri, G. Thouvenin, 2013, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Idiopathic eosinophilic pneumonia in children: the French experience

T. Leblanc, A. Clément, J. Dubus, 2014, Orphanet Journal of Rare Diseases.

A rare CFTR intronic mutation related to a mild CF disease in a 12-year-old girl

A. Clément, E. Girodon, H. Corvol, 2012, BMJ Case Reports.

Unusual presentation of more common disease/injury A rare CFTR intronic mutation related to a mild CF disease in a 12-year-old girl

A. Clément, E. Girodon, H. Corvol, 2012 .

Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective

P. Dieudé, R. Borie, M. Griese, 2022, Diagnostics.

SARS-CoV-2 variant Delta infects all 6 siblings but spares Comirnaty (BNT162b2, BioNTech/Pfizer)-vaccinated parents

H. Corvol, N. Nathan, A. Schnuriger, 2021, The Journal of infectious diseases.

Respiratory Distress, Congenital Hypothyroidism and Hypotonia in a Newborn

A. Clément, R. Borie, D. Doummar, 2016, Respiration.

Diffuse parenchymal lung disease caused by surfactant deficiency: dramatic improvement by azithromycin

R. Epaud, A. Clément, G. Thouvenin, 2013, BMJ Case Reports.

Nutritional Status in Childhood as a Prognostic Factor in Patients with Cystic Fibrosis

D. Vilozni, N. Nathan, I. Sarouk, 2019, Lung.

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

C. Delacourt, P. Reix, R. Epaud, 2022, European Journal of Pediatrics.

The Wide Spectrum of COVID-19 Clinical Presentation in Children

G. Thouvenin, H. Corvol, N. Nathan, 2020, Journal of clinical medicine.

Interstitial lung diseases in children

R. Epaud, A. Clément, B. Fauroux, 2010, Orphanet journal of rare diseases.

Atypical presentation of COVID-19 in young infants

H. Corvol, N. Nathan, Blandine Prévost, 2020, The Lancet.

COVID‐19 and pediatric pulmonology: Feedback from an expert center after the first year of the pandemic

G. Thouvenin, H. Corvol, N. Nathan, 2022, Pediatric pulmonology.

Macrolides: new therapeutic perspectives in lung diseases.

L. Guillot, A. Clément, H. Corvol, 2011, The international journal of biochemistry & cell biology.

Interstitial lung disease: physiopathology in the context of lung growth.

A. Clément, B. Fauroux, G. Thouvenin, 2011, Paediatric respiratory reviews.

MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease

M. Nalls, C. Blauwendraat, D. Schwartz, 2018, The New England journal of medicine.

Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis

P. Boelle, A. Clément, B. Fauroux, 2007, Respiratory research.

Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis

P. Froguel, C. Béroud, A. Bonnefond, 2017, European Respiratory Journal.

Whole exome sequencing in three families segregating a pediatric case of sarcoidosis

J. Bernaudin, S. Pinson, V. Cottin, 2018, BMC Medical Genomics.

Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.

B. Housset, S. Amselem, R. Epaud, 2013, American journal of human genetics.

Management of suspected monogenic lung fibrosis in a specialised centre

L. Gouya, R. Borie, B. Crestani, 2017, European Respiratory Review.

Familial pulmonary fibrosis.

R. Borie, B. Crestani, C. Kannengiesser, 2015, Revue des maladies respiratoires.

Efficacy of Blebs Detection for Preventive Surgery in Children’s Idiopathic Spontaneous Pneumothorax

Marion Lenoir, R. Epaud, A. Clément, 2009, World Journal of Surgery.

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

C. Delacourt, J. Vibert, P. Reix, 2012, Orphanet Journal of Rare Diseases.

An idiopathic congenital chylothorax: surgery or conservative management?

H. Corvol, N. Nathan, M. Larroquet, 2014, BMJ Case Reports.

Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling

T. Molina, Y. Crow, J. Marsh, 2020, The Journal of experimental medicine.

Diagnostic workup of childhood interstitial lung disease

R. Epaud, M. Griese, N. Nathan, 2023, European Respiratory Review.

Exposure to inorganic particles in paediatric sarcoidosis: the PEDIASARC study

C. Delacourt, R. Epaud, A. Clément, 2021, Thorax.

Pulmonary Fibrosis in Children

A. Clément, H. Ducou le Pointe, G. Thouvenin, 2019, Journal of clinical medicine.

Management of children with interstitial lung diseases: the difficult issue of acute exacerbations

R. Epaud, A. Clément, A. Bush, 2016, European Respiratory Journal.

Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer.

S. Amselem, L. Gouya, A. Clément, 2016, Human molecular genetics.

Germline SFTPA 1 mutation in familial idiopathic interstitial pneumonia and lung cancer

S. Amselem, L. Gouya, A. Clément, 2016 .

Physiologic benefits of mechanical insufflation-exsufflation in children with neuromuscular diseases.

A. Clément, F. Lofaso, B. Fauroux, 2008, Chest.

C. Delacourt, P. Reix, P. Boelle, 2019, Pediatric pulmonology.

Long-term effects of azithromycin in patients with cystic fibrosis.

P. Boelle, A. Clément, H. Corvol, 2016, Respiratory medicine.

Functional assessment and phenotypic heterogeneity of SFTPA1 and SFTPA2 mutations in interstitial lung diseases and lung cancer

S. Leroy, J. Dalphin, A. Cazes, 2020, European Respiratory Journal.

AB0007 Shared genetic predisposition in rheumatoid arthritis–interstitial lung disease and familial pulmonary fibrosis

P. Revy, S. Gazal, P. Dieudé, 2017 .

Children’s views on artificial intelligence and digital twins for the daily management of their asthma: a mixed-method study

C. Delacourt, D. Drummond, A. Hadchouel, 2022, European Journal of Pediatrics.

Diffuse alveolar haemorrhage in children: an international multicentre study

P. Reix, A. Clément, N. Kiper, 2023, ERJ Open Research.

Work of breathing in children with diffuse parenchymal lung disease

C. Delacourt, A. Clément, B. Fauroux, 2015, Respiratory Physiology & Neurobiology.

Usefulness of bronchoalveolar lavage in a French pediatric cohort with hypersensitivity pneumonitis

P. Reix, G. Reboux, A. Deschildre, 2020, Pediatric pulmonology.

Whole exome sequencing in three families segregating a pediatric case of sarcoidosis

J. Bernaudin, S. Pinson, V. Cottin, 2018, BMC Medical Genomics.

Familial vs. sporadic sarcoidosis: BTNL2 polymorphisms, clinical presentations, and outcomes in a French cohort

M. Elsensohn, J. Piette, R. Roussel, 2016, Orphanet Journal of Rare Diseases.

A Nonsmoker Man in His 40s With a Diagnosis of Genetic‐Related Idiopathic Pulmonary Fibrosis (Surfactant‐Protein C Gene Mutation)

M. Ohana, M. Legendre, M. Chenard, 2019, Chest.

Biomarkers in Interstitial lung diseases.

S. Amselem, A. Clément, H. Corvol, 2015, Paediatric respiratory reviews.

Ultrasonography and Computed Tomographic Manifestations of Abdominal Sarcoidosis in Children

R. Epaud, P. Tounian, E. Blondiaux, 2016, Journal of pediatric gastroenterology and nutrition.

Pulmonary sarcoid-like granulomatous disease in an 11-month-old girl

H. Corvol, N. Nathan, J. Pautrat, 2013, BMJ Case Reports.

Interstitial lung diseases

A. Clément, G. Thouvenin, H. Corvol, 2021, ERS Handbook of Paediatric Respiratory Medicine.

Diffuse alveolar haemorrhage in children: an international multicentre study

P. Reix, A. Clément, N. Kiper, 2021, ERJ Open Research.

Outcome of lung transplantation for adults with interstitial lung disease associated with genetic disorders of the surfactant system

V. Cottin, R. Borie, M. Reynaud‐Gaubert, 2023, ERJ open research.

Hypomorphic pathogenic variant in SFTPB leads to adult pulmonary fibrosis

S. Amselem, G. Prévot, A. Coulomb, 2023, European Journal of Human Genetics.

Genetic testing in idiopathic interstitial pneumonia

C. Delacourt, P. Reix, S. Amselem, 2015 .

Contribution Of Mutations In Genes Encoding Proteins Of The Surfactant Metabolism To Idiopathic Interstitial Pneumonia And Idiopathic Pulmonary Fibrosis In A Cohort Of 265 Families

C. Delacourt, P. Reix, S. Amselem, 2016 .