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Mutation in RAP1 is a rare event in myelodysplastic syndromes.
Gyan E, Frew M, Bowen D, Beldjord C, Preudhomme C, Lacombe C, Mayeux P, Dreyfus F, Porteu F, Fontenay M. Gyan E, et al. Among authors: fontenay m. Leukemia. 2005 Sep;19(9):1678-80. doi: 10.1038/sj.leu.2403882. Leukemia. 2005. PMID: 16118622 No abstract available.
A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture.
Veyradier A, Boisseau P, Fressinaud E, Caron C, Ternisien C, Giraud M, Zawadzki C, Trossaert M, Itzhar-Baïkian N, Dreyfus M, d'Oiron R, Borel-Derlon A, Susen S, Bezieau S, Denis CV, Goudemand J; French Reference Center for von Willebrand disease. Veyradier A, et al. Medicine (Baltimore). 2016 Mar;95(11):e3038. doi: 10.1097/MD.0000000000003038. Medicine (Baltimore). 2016. PMID: 26986123 Free PMC article.
[Pathophysiology of myelodysplastic syndromes].
Fontenay M, Boussaid I, Chapuis N. Fontenay M, et al. Bull Cancer. 2023 Nov;110(11):1097-1105. doi: 10.1016/j.bulcan.2023.02.026. Epub 2023 Jul 7. Bull Cancer. 2023. PMID: 37423830 Review. French.
Multiparameter flow cytometry in the evaluation of myelodysplasia: Analytical issues: Recommendations from the European LeukemiaNet/International Myelodysplastic Syndrome Flow Cytometry Working Group.
Porwit A, Béné MC, Duetz C, Matarraz S, Oelschlaegel U, Westers TM, Wagner-Ballon O, Kordasti S, Valent P, Preijers F, Alhan C, Bellos F, Bettelheim P, Burbury K, Chapuis N, Cremers E, Della Porta MG, Dunlop A, Eidenschink-Brodersen L, Font P, Fontenay M, Hobo W, Ireland R, Johansson U, Loken MR, Ogata K, Orfao A, Psarra K, Saft L, Subira D, Te Marvelde J, Wells DA, van der Velden VHJ, Kern W, van de Loosdrecht AA. Porwit A, et al. Among authors: fontenay m. Cytometry B Clin Cytom. 2023 Jan;104(1):27-50. doi: 10.1002/cyto.b.22108. Epub 2022 Dec 20. Cytometry B Clin Cytom. 2023. PMID: 36537621 Free PMC article. Review.
167 results