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Autoimmune hypoglycemia expands the biological spectrum of HHV8+ multicentric Castleman disease.
Arnautou P, Auclair M, Fellahi S, Bouché C, Fieschi C, Barrak E, Queyrel-Moranne V, Chaillous L, Blin N, Malphettes M, Fadlallah J, Bertinchamp R, Gérard L, Bengoufa D, Galicier L, Oksenhendler E, Vigouroux C, Boutboul D. Arnautou P, et al. Among authors: barrak e. Blood Adv. 2021 Apr 13;5(7):1848-1852. doi: 10.1182/bloodadvances.2020002801. Blood Adv. 2021. PMID: 33787862 Free PMC article.
Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia.
Rimbert A, Pichelin M, Lecointe S, Marrec M, Le Scouarnec S, Barrak E, Croyal M, Krempf M, Le Marec H, Redon R, Schott JJ, Magré J, Cariou B. Rimbert A, et al. Among authors: barrak e. Atherosclerosis. 2016 Jul;250:52-6. doi: 10.1016/j.atherosclerosis.2016.04.010. Epub 2016 Apr 11. Atherosclerosis. 2016. PMID: 27179706 Free article.