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An in-house assay is superior to Sepsityper for direct matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry identification of yeast species in blood cultures.
Bidart M, Bonnet I, Hennebique A, Kherraf ZE, Pelloux H, Berger F, Cornet M, Bailly S, Maubon D. Bidart M, et al. Among authors: berger f. J Clin Microbiol. 2015 May;53(5):1761-4. doi: 10.1128/JCM.03600-14. Epub 2015 Mar 11. J Clin Microbiol. 2015. PMID: 25762771 Free PMC article.
[Anti-angiogenic therapies: from theory to practice].
Bidart M, Berger F, Pelletier L. Bidart M, et al. Among authors: berger f. Ann Biol Clin (Paris). 2013 Sep-Oct;71(5):527-35. doi: 10.1684/abc.2013.0883. Ann Biol Clin (Paris). 2013. PMID: 24113438 Free article. Review. French.
In vivo quantification of magnetically labelled cells by MRI relaxometry.
Gimenez U, Lajous H, El Atifi M, Bidart M, Auboiroux V, Fries PH, Berger F, Lahrech H. Gimenez U, et al. Among authors: berger f. Contrast Media Mol Imaging. 2016 Nov;11(6):535-543. doi: 10.1002/cmmi.1715. Epub 2016 Oct 21. Contrast Media Mol Imaging. 2016. PMID: 27766757 Free article.
Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic features.
Bidart M, El Atifi M, Miladi S, Rendu J, Satre V, Ray PF, Bosson C, Devillard F, Lehalle D, Malan V, Amiel J, Mencarelli MA, Baldassarri M, Renieri A, Clayton-Smith J, Vieville G, Thevenon J, Amblard F, Berger F, Jouk PS, Coutton C. Bidart M, et al. Among authors: berger f. Genet Med. 2017 Jun;19(6):701-710. doi: 10.1038/gim.2016.180. Epub 2016 Dec 1. Genet Med. 2017. PMID: 27906199 Free article.
Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction.
Petre G, Lorès P, Sartelet H, Truffot A, Poreau B, Brandeis S, Martinez G, Satre V, Harbuz R, Ray PF, Amblard F, Devillard F, Vieville G, Berger F, Jouk PS, Vaiman D, Touré A, Coutton C, Bidart M. Petre G, et al. Among authors: berger f. Clin Genet. 2018 Dec;94(6):575-580. doi: 10.1111/cge.13449. Epub 2018 Oct 17. Clin Genet. 2018. PMID: 30221343
1,852 results