Metabolic Interplay between Peroxisomes and Other Subcellular Organelles Including Mitochondria and the Endoplasmic Reticulum

by Wanders, Ronald J. A., Waterham, Hans R., Ferdinandusse, Sacha
Published 2016

Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene

by Sevin, Caroline, Ferdinandusse, Sacha, Waterham, Hans R, Wanders, Ronald J, Aubourg, Patrick
Published 2011

Peroxisomal Targeting, Import, and Assembly of Alcohol Oxidase in Pichia pastoris

by Waterham, Hans R., Russell, Kimberly A., de Vries, Yne, Cregg, James M.
Published 1997

The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives

by Bosch, Annet M, Stroek, Kevin, Abeling, Nico G, Waterham, Hans R, IJlst, Lodewijk, Wanders, Ronald JA
Published 2012

Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorder

by Berendse, Kevin, Ebberink, Merel S, IJlst, Lodewijk, Poll-The, Bwee Tien, Wanders, Ronald J A, Waterham, Hans R
Published 2013

The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders

by Ferdinandusse, Sacha, Ebberink, Merel S., Vaz, Frédéric M., Waterham, Hans R., Wanders, Ronald J. A.
Published 2016

Peroxisomal ABC transporters: functions and mechanism

by Baker, Alison, Carrier, David J., Schaedler, Theresia, Waterham, Hans R., van Roermund, Carlo W., Theodoulou, Frederica L.
Published 2015

Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS)

by Messer, Laurent, Alsaleh, Ghada, Georgel, Philippe, Carapito, Raphael, Waterham, Hans R, Dali-Youcef, Nassim, Bahram, Siamak, Sibilia, Jean
Published 2016

Alkyl-Glycerol Rescues Plasmalogen Levels and Pathology of Ether-Phospholipid Deficient Mice

by Brites, Pedro, Ferreira, Ana Sofia, Ferreira da Silva, Tiago, Sousa, Vera F., Malheiro, Ana R., Duran, Marinus, Waterham, Hans R., Baes, Myriam, Wanders, Ronald J. A.
Published 2011

The Proteome of Human Liver Peroxisomes: Identification of Five New Peroxisomal Constituents by a Label-Free Quantitative Proteomics Survey

by Gronemeyer, Thomas, Wiese, Sebastian, Ofman, Rob, Bunse, Christian, Pawlas, Magdalena, Hayen, Heiko, Eisenacher, Martin, Stephan, Christian, Meyer, Helmut E., Waterham, Hans R., Erdmann, Ralf, Wanders, Ronald J., Warscheid, Bettina
Published 2013

Correction: The Proteome of Human Liver Peroxisomes: Identification of Five New Peroxisomal Constituents by a Label-Free Quantitative Proteomics Survey

by Gronemeyer, Thomas, Wiese, Sebastian, Ofman, Rob, Bunse, Christian, Pawlas, Magdalena, Hayen, Heiko, Eisenacher, Martin, Stephan, Christian, Meyer, Helmut E., Waterham, Hans R., Erdmann, Ralf, Wanders, Ronald J., Warscheid, Bettina
Published 2013

Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood

by Berendse, Kevin, Engelen, Marc, Ferdinandusse, Sacha, Majoie, Charles B. L. M., Waterham, Hans R., Vaz, Frédéric M., Koelman, Johannes H. T. M., Barth, Peter G., Wanders, Ronald J. A., Poll-The, Bwee Tien
Published 2015

Barley has two peroxisomal ABC transporters with multiple functions in β-oxidation

by Mendiondo, Guillermina M., Medhurst, Anne, van Roermund, Carlo W., Zhang, Xuebin, Devonshire, Jean, Scholefield, Duncan, Fernández, José, Axcell, Barry, Ramsay, Luke, Waterham, Hans R., Waugh, Robbie, Theodoulou, Frederica L., Holdsworth, Michael J.
Published 2014

HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase

by Ferdinandusse, Sacha, Waterham, Hans R, Heales, Simon JR, Brown, Garry K, Hargreaves, Iain P, Taanman, Jan-Willem, Gunny, Roxana, Abulhoul, Lara, Wanders, Ronald JA, Clayton, Peter T, Leonard, James V, Rahman, Shamima
Published 2013

Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study

by Touw, Catharina M L, Smit, G Peter A, de Vries, Maaike, de Klerk, Johannis B C, Bosch, Annet M, Visser, Gepke, Mulder, Margot F, Rubio-Gozalbo, M Estela, Elvers, Bert, Niezen-Koning, Klary E, Wanders, Ronald J A, Waterham, Hans R, Reijngoud, Dirk-Jan, Derks, Terry G J
Published 2012

Cholic acid therapy in Zellweger spectrum disorders

by 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
Published 2016

Clinical and biochemical characterization of four patients with mutations in ECHS1

by Ferdinandusse, Sacha, Friederich, Marisa W., Burlina, Alberto, Ruiter, Jos P. N., Coughlin, Curtis R., Dishop, Megan K., Gallagher, Renata C., Bedoyan, Jirair K., Vaz, Frédéric M., Waterham, Hans R., Gowan, Katherine, Chatfield, Kathryn, Bloom, Kaitlyn, Bennett, Michael J., Elpeleg, Orly, Van Hove, Johan L. K., Wanders, Ronald J. A.
Published 2015