Endothelial Dysfunction in Fabry Disease Is Related to Glycocalyx Degradation

por Solvey Pollmann, David Scharnetzki, Dominique Manikowski, Malte Lenders, Eva Brand
Publicado 2021

α-Galactosidase a Deficiency in Fabry Disease Leads to Extensive Dysregulated Cellular Signaling Pathways in Human Podocytes

por Ulrich Jehn, Samet Bayraktar, Solvey Pollmann, Veerle Van Marck, Thomas Weide, Hermann Pavenstädt, Eva Brand, Malte Lenders
Publicado 2021

Multifocal white matter lesions associated with the D313Y mutation of the α-galactosidase A gene.

por Malte Lenders, Thomas Duning, Michael Schelleckes, Boris Schmitz, Sonja Stander, Arndt Rolfs, Stefan-Martin Brand, Eva Brand
Publicado 2013

Circulating microRNAs in Fabry Disease

por Ke Xiao, Dongchao Lu, Jeannine Hoepfner, Laura Santer, Shashi Gupta, Angelika Pfanne, Sabrina Thum, Malte Lenders, Eva Brand, Peter Nordbeck, Thomas Thum
Publicado 2019