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  1. Article ; Online: Childhood Interstitial Lung Diseases (chILD) Recognition: When Epidemiology Increases a Rare Disease Incidence.

    Nathan, Nadia

    Archivos de bronconeumologia

    2022  Volume 58, Issue 3, Page(s) 217–218

    Language Spanish
    Publishing date 2022-01-23
    Publishing country Spain
    Document type Editorial
    ZDB-ID 733126-5
    ISSN 1579-2129 ; 0300-2896
    ISSN (online) 1579-2129
    ISSN 0300-2896
    DOI 10.1016/j.arbres.2022.01.009
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  2. Article ; Online: Elexacaftor/tezacaftor/ivacaftor can rescue pancreatic function in F508del homozygous children.

    Nathan, Nadia / Thouvenin, Guillaume / Dubern, Béatrice / Corvol, Harriet

    Pediatric pulmonology

    2023  Volume 59, Issue 3, Page(s) 788–790

    MeSH term(s) Child ; Humans ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics ; Aminophenols/therapeutic use ; Mutation ; Benzodioxoles/therapeutic use ; Indoles ; Pyrazoles ; Pyridines ; Pyrrolidines ; Quinolones
    Chemical Substances elexacaftor (RRN67GMB0V) ; ivacaftor (1Y740ILL1Z) ; tezacaftor ; Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6) ; Aminophenols ; Benzodioxoles ; Indoles ; Pyrazoles ; Pyridines ; Pyrrolidines ; Quinolones
    Language English
    Publishing date 2023-12-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 632784-9
    ISSN 1099-0496 ; 8755-6863
    ISSN (online) 1099-0496
    ISSN 8755-6863
    DOI 10.1002/ppul.26794
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  3. Article ; Online: Spontaneous pneumomediastinum: A complication of SARS-CoV-2 variant delta infection in children.

    Prevost, Blandine / Leger, Pierre-Louis / Sileo, Chiara / Corvol, Fany / Lecarpentier, Thibault / Nathan, Nadia / Corvol, Harriet

    Pediatric pulmonology

    2024  

    Language English
    Publishing date 2024-02-23
    Publishing country United States
    Document type Letter
    ZDB-ID 632784-9
    ISSN 1099-0496 ; 8755-6863
    ISSN (online) 1099-0496
    ISSN 8755-6863
    DOI 10.1002/ppul.26931
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  4. Article ; Online: 50 Years Ago in TheJournalofPediatrics: Disappearance of Reye Syndrome Outbreaks: One of the Greatest Public Health Victories.

    Ovchinsky, Nadia / Litman, Nathan

    The Journal of pediatrics

    2021  Volume 243, Page(s) 207

    MeSH term(s) Disease Outbreaks ; Humans ; Public Health ; Reye Syndrome
    Language English
    Publishing date 2021-12-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3102-1
    ISSN 1097-6833 ; 0022-3476
    ISSN (online) 1097-6833
    ISSN 0022-3476
    DOI 10.1016/j.jpeds.2021.12.065
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  5. Article ; Online: Pulmonary mucoepidermoid carcinoma in a 7-year-old child.

    Denamur, Sophie / Hervieux, Erik / Cosson, Laure / Sileo, Chiara / Coulomb, Aurore / Nathan, Nadia / Corvol, Harriet

    Pediatric pulmonology

    2024  Volume 59, Issue 4, Page(s) 1095–1098

    Abstract: A 7-year-old boy presented with exertional dyspnea and cough, initially misdiagnosed as asthma. Imaging revealed a mass obstructing the left main bronchus, later identified as a pulmonary mucoepidermoid carcinoma (MEC). Following surgical sleeve ... ...

    Abstract A 7-year-old boy presented with exertional dyspnea and cough, initially misdiagnosed as asthma. Imaging revealed a mass obstructing the left main bronchus, later identified as a pulmonary mucoepidermoid carcinoma (MEC). Following surgical sleeve resection, complete tumor removal occurred without malignancy in surrounding lymph nodes, resulting in symptom resolution without additional therapy. Pulmonary MEC, uncommon in pediatric patients, poses diagnostic challenges due to nonspecific symptoms, resulting in delayed diagnosis. Typically managed via complete surgical resection, MEC offers a favorable prognosis, primarily affecting central airways and requiring conservative surgical approaches to preserve lung tissue. This case underscores the diagnostic challenges of primary pulmonary MEC in pediatric patients. It stresses the need to consider unusual causes in pediatric respiratory symptoms and highlights the critical role of precise diagnostic methods and personalized surgical strategies in managing such rare pulmonary malignancies for optimal outcomes.
    MeSH term(s) Male ; Humans ; Child ; Carcinoma, Mucoepidermoid/diagnostic imaging ; Carcinoma, Mucoepidermoid/surgery ; Lung Neoplasms/diagnostic imaging ; Lung Neoplasms/surgery ; Lung Neoplasms/pathology ; Prognosis ; Bronchi/pathology ; Asthma
    Language English
    Publishing date 2024-01-15
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 632784-9
    ISSN 1099-0496 ; 8755-6863
    ISSN (online) 1099-0496
    ISSN 8755-6863
    DOI 10.1002/ppul.26864
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  6. Article ; Online: Long-Term Respiratory Outcome of Children with Empyema.

    Jalunis, Mohamed Mustakim / Hng, Shih Ying / Eg, Kah Peng / Gowdh, Nadia Fareeda Muhammad / Sanmugam, Anand / Nah, Shireen Anne / Nathan, Anna Marie / de Bruyne, Jessie Anne

    Indian journal of pediatrics

    2024  

    Language English
    Publishing date 2024-01-15
    Publishing country India
    Document type Letter
    ZDB-ID 218231-2
    ISSN 0973-7693 ; 0019-5456
    ISSN (online) 0973-7693
    ISSN 0019-5456
    DOI 10.1007/s12098-024-05021-4
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  7. Article ; Online: COPA syndrome, 5 years after: Where are we?

    Frémond, Marie-Louise / Nathan, Nadia

    Joint bone spine

    2020  Volume 88, Issue 2, Page(s) 105070

    Abstract: Heterozygous missense mutations in COPA, encoding coatomer protein subunit alpha (COPA), cause an interferonopathy mainly associating lung, joint and kidney involvement. This rare autoinflammatory disease is characterised by variable expression and a ... ...

    Abstract Heterozygous missense mutations in COPA, encoding coatomer protein subunit alpha (COPA), cause an interferonopathy mainly associating lung, joint and kidney involvement. This rare autoinflammatory disease is characterised by variable expression and a remarkably high frequency of clinical non-penetrance. Lung features, predominantly chronic diffuse alveolar haemorrhage (DAH), are observed in almost patients and can result in end-stage respiratory insufficiency. The initially described phenotype was broadened to include isolated DAH or lupus nephritis. Rare manifestations reminiscent of other monogenic interferonopathies occur. This indicates the need for careful clinical evaluation in patients with suspicion or diagnosis of COPA syndrome. Considering the dominant inheritance model and the highly variable phenotype, ranging from severe multi-organic disorder to non-penetrance, a careful family screening is recommended. New insights in disease pathogenesis have linked COPA mutations to STING-mediated interferon signalling. Beside a variable efficacy of 'classical' immunosuppressive drugs, Janus kinase (JAK) inhibitors constitute a promising treatment in COPA syndrome, and further targeted therapies are awaited.
    MeSH term(s) Coatomer Protein/genetics ; Heterozygote ; Humans ; Lung Diseases ; Mutation, Missense ; Syndrome
    Chemical Substances Coatomer Protein
    Language English
    Publishing date 2020-09-09
    Publishing country France
    Document type Journal Article
    ZDB-ID 2020487-5
    ISSN 1778-7254 ; 1297-319X
    ISSN (online) 1778-7254
    ISSN 1297-319X
    DOI 10.1016/j.jbspin.2020.09.002
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  8. Article ; Online: Atypical presentation of COVID-19 in young infants.

    Nathan, Nadia / Prevost, Blandine / Corvol, Harriet

    Lancet (London, England)

    2020  Volume 395, Issue 10235, Page(s) 1481

    MeSH term(s) Betacoronavirus ; COVID-19 ; Child ; Coronavirus ; Coronavirus Infections ; Humans ; Infant ; Pandemics ; Pneumonia, Viral ; SARS-CoV-2
    Keywords covid19
    Language English
    Publishing date 2020-04-27
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 3306-6
    ISSN 1474-547X ; 0023-7507 ; 0140-6736
    ISSN (online) 1474-547X
    ISSN 0023-7507 ; 0140-6736
    DOI 10.1016/S0140-6736(20)30980-6
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  9. Article ; Online: Parkin Mediates Cannabidiol Prevention of Amyloid-Beta-Induced Senescence in Human Astrocytes.

    Wang, Zhizhen / Zheng, Peng / Nagaratnam, Nathan / Solowij, Nadia / Huang, Xu-Feng

    Cannabis and cannabinoid research

    2023  Volume 8, Issue 2, Page(s) 309–320

    Abstract: Introduction: ...

    Abstract Introduction:
    MeSH term(s) Animals ; Humans ; Cannabidiol/pharmacology ; Astrocytes/metabolism ; Astrocytes/pathology ; Reactive Oxygen Species/metabolism ; Reactive Oxygen Species/pharmacology ; Caenorhabditis elegans/metabolism ; Amyloid beta-Peptides/metabolism ; Amyloid beta-Peptides/pharmacology ; Alzheimer Disease/drug therapy ; Alzheimer Disease/metabolism ; Alzheimer Disease/pathology ; Ubiquitin-Protein Ligases/metabolism ; Ubiquitin-Protein Ligases/pharmacology
    Chemical Substances Cannabidiol (19GBJ60SN5) ; Reactive Oxygen Species ; Amyloid beta-Peptides ; Ubiquitin-Protein Ligases (EC 2.3.2.27)
    Language English
    Publishing date 2023-01-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2867624-5
    ISSN 2378-8763 ; 2578-5125
    ISSN (online) 2378-8763
    ISSN 2578-5125
    DOI 10.1089/can.2022.0186
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  10. Article ; Online: Severe Acute Respiratory Syndrome Coronavirus 2 Variant Delta Infects All 6 Siblings but Spares Comirnaty (BNT162b2, BioNTech/Pfizer)-Vaccinated Parents.

    Nathan, Nadia / Prevost, Blandine / Lambert, Sidonie / Schnuriger, Aurélie / Corvol, Harriet

    The Journal of infectious diseases

    2021  Volume 224, Issue 11, Page(s) 1984–1986

    MeSH term(s) BNT162 Vaccine ; COVID-19 ; Humans ; Parents ; SARS-CoV-2 ; Siblings
    Chemical Substances BNT162 Vaccine (N38TVC63NU)
    Language English
    Publishing date 2021-11-09
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiab410
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