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Olivier Dormond

As seen in: MDPI, Swiss Medical Weekly
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Articles

Characterization of Renal Cell Carcinoma Heterotypic 3D Co-Cultures with Immune Cell Subsets

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By Magdalena Rausch, Olivier Dormond, Patrycja Nowak-Sliwinska, Léa Blanc
| MDPI
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Swiss Medical Weekly - Article

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By Juerg Schwitter, Pierre Monney, Salah Dine Qanadli, Steven Hajdu, Christel Tran, Olivier Dormond, Frédéric Barbey
| Swiss Medical Weekly Verified
Fabry disease is a rare X-linked disorder caused by deficiency of the lysosomal enzyme alpha-galactosidase A (?-Gal A). This defect leads to progressive accumulation of glycosphingolipids (GSL) in many tissues and organs, and in particular in endothelial and vascular smooth muscle cells (VSMC) of the arterial tree [1]. Males affected by the classic form of the disease, defined as a residual ?-Gal A activity <1%, develop vascular abnormalities.
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