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Year Number of Results
2006 1
2009 1
2010 3
2011 3
2012 3
2013 4
2014 1
2015 1
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2017 3
2019 2
2020 1
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2022 6
2023 6
2024 1

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34 results

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Page 1
Structure-Based Understanding of ABCA3 Variants.
Onnée M, Fanen P, Callebaut I, de Becdelièvre A. Onnée M, et al. Among authors: de becdelievre a. Int J Mol Sci. 2021 Sep 24;22(19):10282. doi: 10.3390/ijms221910282. Int J Mol Sci. 2021. PMID: 34638622 Free PMC article.
SCN10A variants associated with congenital harlequin syndrome.
Halle A, De Becdelievre A, Funalot B, Labrèze C, Morice-Picard F, Boralevi F. Halle A, et al. Among authors: de becdelievre a. Br J Dermatol. 2022 Jun;186(6):1039-1041. doi: 10.1111/bjd.21011. Epub 2022 Mar 22. Br J Dermatol. 2022. PMID: 35007332 No abstract available.
Instability of Mature ABCA3 Protein: Toward a New Classification of ABCA3 Mutations?
Onnée M, Duriez B, Simon S, Szczepaniak C, Guguin A, Epaud R, Hamouda S, Fanen P, de Becdelièvre A. Onnée M, et al. Among authors: de becdelievre a. Am J Respir Cell Mol Biol. 2022 Nov;67(5):602-605. doi: 10.1165/rcmb.2021-0430LE. Am J Respir Cell Mol Biol. 2022. PMID: 36318016 No abstract available.
COMMD1-mediated ubiquitination regulates CFTR trafficking.
Drévillon L, Tanguy G, Hinzpeter A, Arous N, de Becdelièvre A, Aissat A, Tarze A, Goossens M, Fanen P. Drévillon L, et al. Among authors: de becdelievre a. PLoS One. 2011 Mar 31;6(3):e18334. doi: 10.1371/journal.pone.0018334. PLoS One. 2011. PMID: 21483833 Free PMC article.
AQP5, a second gene at play with CFTR in aquagenic palmoplantar keratoderma.
Sperelakis-Beedham B, Lopez M, Bourrat E, Gaitch N, Houriez F, Martinez B, Fajac I, Burgel PR, Hickman G, Audrézet MP, Gonde D, Cabet F, Gerfaud-Valentin M, Nove-Josserand R, Raynal C, Pagin A, Reboul MP, de Becdelièvre A, Bienvenu T, Callebaut I, Girodon E. Sperelakis-Beedham B, et al. Among authors: de becdelievre a. J Eur Acad Dermatol Venereol. 2023 May;37(5):e654-e657. doi: 10.1111/jdv.18869. Epub 2023 Jan 24. J Eur Acad Dermatol Venereol. 2023. PMID: 36645858 No abstract available.
Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variant.
Delestrain C, Aissat A, Nattes E, Gibertini I, Lacroze V, Simon S, Decrouy X, de Becdelièvre A, Fanen P, Epaud R. Delestrain C, et al. Among authors: de becdelievre a. Front Pediatr. 2023 Jan 17;10:978598. doi: 10.3389/fped.2022.978598. eCollection 2022. Front Pediatr. 2023. PMID: 36733766 Free PMC article.
Congenital surfactant protein B (SP-B) deficiency: a case report.
Khalsi F, Chaabene M, Romdhane MB, Trabelsi I, Hamouda S, de Becdelièvre A, Boussetta K. Khalsi F, et al. Among authors: de becdelievre a. Pan Afr Med J. 2023 Apr 4;44:158. doi: 10.11604/pamj.2023.44.158.35316. eCollection 2023. Pan Afr Med J. 2023. PMID: 37455866 Free PMC article.
Interstitial lung disease reveals 48,XXYY syndrome in a child.
Gros M, Aissat A, Perez-Martin S, Abou Taam R, Funalot B, Fanen P, Epaud R, de Becdelievre A. Gros M, et al. Among authors: de becdelievre a. Acta Paediatr. 2020 May;109(5):1060-1061. doi: 10.1111/apa.15090. Epub 2019 Dec 4. Acta Paediatr. 2020. PMID: 31721284 No abstract available.
Variable Expression of Lung Disease Due to a Novel Homozygous ABCA3 Variant.
Hamouda S, de Becdelièvre A, Ben Ameur S, Trabelsi I, Fabre M, Epaud R, Fanen P, Boussetta K. Hamouda S, et al. Among authors: de becdelievre a. Pediatr Allergy Immunol Pulmonol. 2022 Sep;35(3):124-128. doi: 10.1089/ped.2022.0023. Pediatr Allergy Immunol Pulmonol. 2022. PMID: 36121785
COMMD1 modulates noxious inflammation in cystic fibrosis.
de Becdelièvre A, Rocca J, Aissat A, Drévillon L, Moutereau S, Le Gouvello S, Hinzpeter A, Tarze A, Fanen P. de Becdelièvre A, et al. Int J Biochem Cell Biol. 2013 Nov;45(11):2402-9. doi: 10.1016/j.biocel.2013.07.012. Epub 2013 Jul 24. Int J Biochem Cell Biol. 2013. PMID: 23892095
34 results