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Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults.
Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaimé F, Dragon-Durey MA, Ngo S, Moulin B, Servais A, Provot F, Rostaing L, Burtey S, Niaudet P, Deschênes G, Lebranchu Y, Zuber J, Loirat C. Fremeaux-Bacchi V, et al. Among authors: ngo s. Clin J Am Soc Nephrol. 2013 Apr;8(4):554-62. doi: 10.2215/CJN.04760512. Epub 2013 Jan 10. Clin J Am Soc Nephrol. 2013. PMID: 23307876 Free PMC article.
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.
Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, Macher MA, Zuber J, Karras A, Provot F, Moulin B, Grünfeld JP, Niaudet P, Lesavre P, Frémeaux-Bacchi V. Servais A, et al. Among authors: ngo s. Kidney Int. 2012 Aug;82(4):454-64. doi: 10.1038/ki.2012.63. Epub 2012 Mar 28. Kidney Int. 2012. PMID: 22456601 Free article.
Anti-factor H autoantibodies assay.
Dragon-Durey MA, Blanc C, Roumenina LT, Poulain N, Ngo S, Bordereau P, Frémeaux-Bacchi V. Dragon-Durey MA, et al. Among authors: ngo s. Methods Mol Biol. 2014;1100:249-56. doi: 10.1007/978-1-62703-724-2_20. Methods Mol Biol. 2014. PMID: 24218265
Complement factor B mutations in atypical hemolytic uremic syndrome-disease-relevant or benign?
Marinozzi MC, Vergoz L, Rybkine T, Ngo S, Bettoni S, Pashov A, Cayla M, Tabarin F, Jablonski M, Hue C, Smith RJ, Noris M, Halbwachs-Mecarelli L, Donadelli R, Fremeaux-Bacchi V, Roumenina LT. Marinozzi MC, et al. Among authors: ngo s. J Am Soc Nephrol. 2014 Sep;25(9):2053-65. doi: 10.1681/ASN.2013070796. Epub 2014 Mar 20. J Am Soc Nephrol. 2014. PMID: 24652797 Free PMC article.
[Complement deficiencies and human diseases].
Rosain J, Ngo S, Bordereau P, Poulain N, Roncelin S, Vieira Martins P, Dragon-Durey MA, Frémeaux-Bacchi V. Rosain J, et al. Among authors: ngo s. Ann Biol Clin (Paris). 2014 May-Jun;72(3):271-80. doi: 10.1684/abc.2014.0961. Ann Biol Clin (Paris). 2014. PMID: 24876138 Free article. Review. French.
Standardisation of the factor H autoantibody assay.
Watson R, Lindner S, Bordereau P, Hunze EM, Tak F, Ngo S, Zipfel PF, Skerka C, Dragon-Durey MA, Marchbank KJ. Watson R, et al. Among authors: ngo s. Immunobiology. 2014 Jan;219(1):9-16. doi: 10.1016/j.imbio.2013.06.004. Epub 2013 Jun 26. Immunobiology. 2014. PMID: 23891327
C3 nephritic factor associated with C3 glomerulopathy in children.
Nicolas C, Vuiblet V, Baudouin V, Macher MA, Vrillon I, Biebuyck-Gouge N, Dehennault M, Gié S, Morin D, Nivet H, Nobili F, Ulinski T, Ranchin B, Marinozzi MC, Ngo S, Frémeaux-Bacchi V, Pietrement C. Nicolas C, et al. Among authors: ngo s. Pediatr Nephrol. 2014 Jan;29(1):85-94. doi: 10.1007/s00467-013-2605-6. Epub 2013 Sep 26. Pediatr Nephrol. 2014. PMID: 24068526
[Agranulocytosis related to fluindione: A case report].
Ngo S, Benhamou Y, Armengol G, Sauvêtre G, Cailleux-Talbot N, Massy N, Buchonnet G, Lévesque H. Ngo S, et al. Rev Med Interne. 2016 Jan;37(1):58-61. doi: 10.1016/j.revmed.2015.05.013. Epub 2015 Jun 18. Rev Med Interne. 2016. PMID: 26096756 French.
368 results