Reply: Low bone mineral density is a common feature of Zellweger spectrum disorders

por Klouwer, Femke C.C., Abdulrahman, Hanna, Poll-The, Bwee Tien
Publicado en Mol Genet Metab Rep (2016)

Peroxisomal abnormalities in the immortalized human hepatocyte (IHH) cell line

por Klouwer, Femke C. C., Koster, Janet, Ferdinandusse, Sacha, Waterham, Hans R.
Publicado en Histochem Cell Biol (2016)

Zellweger spectrum disorders: clinical overview and management approach

por Klouwer, Femke C. C., Berendse, Kevin, Ferdinandusse, Sacha, Wanders, Ronald J. A., Engelen, Marc, Poll-The, Bwee Tien
Publicado en Orphanet J Rare Dis (2015)

Coagulopathy in Zellweger spectrum disorders: a role for vitamin K

por Zeynelabidin, Sara, Klouwer, Femke C. C., Meijers, Joost C. M., Suijker, Monique H., Engelen, Marc, Poll-The, Bwee Tien, van Ommen, C. Heleen
Publicado en J Inherit Metab Dis (2017)

Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis Defect

por Klouwer, Femke C. C., Falkenberg, Kim D., Ofman, Rob, Koster, Janet, van Gent, Démi, Ferdinandusse, Sacha, Wanders, Ronald J. A., Waterham, Hans R.
Publicado en Front Cell Dev Biol (2021)

Cholic acid therapy in Zellweger spectrum disorders

por Berendse, Kevin, Klouwer, Femke C. C., Koot, Bart G. P., Kemper, Elles M., Ferdinandusse, Sacha, Koelfat, Kiran V. K., Lenicek, Martin, Schaap, Frank G., Waterham, Hans R., Vaz, Frédéric M., Engelen, Marc, Jansen, Peter L. M., Wanders, Ronald J. A., Poll-The, Bwee Tien
Publicado en J Inherit Metab Dis (2016)

Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder

por Falkenberg, Kim D., Braverman, Nancy E., Moser, Ann B., Steinberg, Steven J., Klouwer, Femke C.C., Schlüter, Agatha, Ruiz, Montserrat, Pujol, Aurora, Engvall, Martin, Naess, Karin, van Spronsen, FrancJan, Körver-Keularts, Irene, Rubio-Gozalbo, M. Estela, Ferdinandusse, Sacha, Wanders, Ronald J.A., Waterham, Hans R.
Publicado en Am J Hum Genet (2017)