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1992 1
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2003 2
2006 3
2007 2
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2011 2
2012 2
2013 3
2014 2
2015 3
2016 6
2017 8
2018 15
2019 9
2020 7
2021 10
2022 7
2023 8
2024 2

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Page 1
International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up.
Altassan R, Péanne R, Jaeken J, Barone R, Bidet M, Borgel D, Brasil S, Cassiman D, Cechova A, Coman D, Corral J, Correia J, de la Morena-Barrio ME, de Lonlay P, Dos Reis V, Ferreira CR, Fiumara A, Francisco R, Freeze H, Funke S, Gardeitchik T, Gert M, Girad M, Giros M, Grünewald S, Hernández-Caselles T, Honzik T, Hutter M, Krasnewich D, Lam C, Lee J, Lefeber D, Marques-de-Silva D, Martinez AF, Moravej H, Õunap K, Pascoal C, Pascreau T, Patterson M, Quelhas D, Raymond K, Sarkhail P, Schiff M, Seroczyńska M, Serrano M, Seta N, Sykut-Cegielska J, Thiel C, Tort F, Vals MA, Videira P, Witters P, Zeevaert R, Morava E. Altassan R, et al. Among authors: borgel d. J Inherit Metab Dis. 2019 Jan;42(1):5-28. doi: 10.1002/jimd.12024. J Inherit Metab Dis. 2019. PMID: 30740725
Pathogenesis of meningococcal purpura fulminans.
Lécuyer H, Borgel D, Nassif X, Coureuil M. Lécuyer H, et al. Among authors: borgel d. Pathog Dis. 2017 Apr 1;75(3). doi: 10.1093/femspd/ftx027. Pathog Dis. 2017. PMID: 28334263 Review.
MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation.
Kauskot A, Mallebranche C, Bruneel A, Fenaille F, Solarz J, Viellard T, Feng M, Repérant C, Bordet JC, Cholet S, Denis CV, McCluskey G, Latour S, Martin E, Pellier I, Lasne D, Borgel D, Kracker S, Ziegler A, Tuffigo M, Fournier B, Miot C, Adam F. Kauskot A, et al. Among authors: borgel d. J Thromb Haemost. 2023 Nov;21(11):3268-3278. doi: 10.1016/j.jtha.2023.05.007. Epub 2023 May 18. J Thromb Haemost. 2023. PMID: 37207862
Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation.
Čechová A, Altassan R, Borgel D, Bruneel A, Correia J, Girard M, Harroche A, Kiec-Wilk B, Mohnike K, Pascreau T, Pawliński Ł, Radenkovic S, Vuillaumier-Barrot S, Aldamiz-Echevarria L, Couce ML, Martins EG, Quelhas D, Morava E, de Lonlay P, Witters P, Honzík T. Čechová A, et al. Among authors: borgel d. J Inherit Metab Dis. 2020 Jul;43(4):671-693. doi: 10.1002/jimd.12241. Epub 2020 Apr 21. J Inherit Metab Dis. 2020. PMID: 32266963 Free PMC article. Review.
Identification of Greb1l as a genetic determinant of crisscross heart in mice showing torsion of the heart tube by shortage of progenitor cells.
Bernheim S, Borgel A, Le Garrec JF, Perthame E, Desgrange A, Michel C, Guillemot L, Sart S, Baroud CN, Krezel W, Raimondi F, Bonnet D, Zaffran S, Houyel L, Meilhac SM. Bernheim S, et al. Among authors: borgel a. Dev Cell. 2023 Nov 6;58(21):2217-2234.e8. doi: 10.1016/j.devcel.2023.09.006. Epub 2023 Oct 17. Dev Cell. 2023. PMID: 37852253
Hemostatic defects in congenital disorders of glycosylation.
Pascreau T, Auditeau C, Borgel D. Pascreau T, et al. Among authors: borgel d. Res Pract Thromb Haemost. 2023 Mar 30;7(3):100142. doi: 10.1016/j.rpth.2023.100142. eCollection 2023 Mar. Res Pract Thromb Haemost. 2023. PMID: 37193126 Free PMC article.
Late-Stage Aromatic C-H Oxygenation.
Börgel J, Tanwar L, Berger F, Ritter T. Börgel J, et al. J Am Chem Soc. 2018 Nov 28;140(47):16026-16031. doi: 10.1021/jacs.8b09208. Epub 2018 Nov 13. J Am Chem Soc. 2018. PMID: 30421917
85 results