Metabolite transport across the peroxisomal membrane

Por Visser, Wouter F., van Roermund, Carlo W. T., Ijlst, Lodewijk, Waterham, Hans R., Wanders, Ronald J. A.
Publicado em 2006

The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results

Por Wanders, Ronald J. A., Ruiter, Jos P. N., IJlst, Lodewijk, Waterham, Hans R., Houten, Sander M.
Publicado em 2010

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

Por Bosch, Annet M, Stroek, Kevin, Abeling, Nico G, Waterham, Hans R, IJlst, Lodewijk, Wanders, Ronald JA
Publicado em 2012

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

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

3-Methylglutaconic Aciduria Type I Is Caused by Mutations in AUH

Por IJlst, Lodewijk, Loupatty, Ference J., Ruiter, Jos P. N., Duran, Marinus, Lehnert, Willy, Wanders, Ronald J. A.
Publicado em 2002

Demonstration and characterization of phosphate transport in mammalian peroxisomes

Por Visser, Wouter F., van Roermund, Carlo W., Ijlst, Lodewijk, Hellingwerf, Klaas J., Wanders, Ronald J. A., Waterham, Hans R.
Publicado em 2005

Prediction of phenotypic severity in mucopolysaccharidosis type IIIA

Por Knottnerus, Suzan J. G., Nijmeijer, Stephanie C. M., IJlst, Lodewijk, te Brinke, Heleen, van Vlies, Naomi, Wijburg, Frits A.
Publicado no Ann Neurol (2017)

Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae

Por van Roermund, Carlo W. T., IJlst, Lodewijk, Majczak, Wiktor, Waterham, Hans R., Folkerts, Hendrik, Wanders, Ronald J. A., Hellingwerf, Klaas J.
Publicado em 2012

Adverse Effects of Genistein in a Mucopolysaccharidosis Type I Mouse Model

Por Kingma, Sandra D. K., Wagemans, Tom, IJlst, Lodewijk, Seppen, Jurgen, Gijbels, Marion J. J., Wijburg, Frits A., van Vlies, Naomi
Publicado no JIMD Rep (2015)

Identification of a Peroxisomal ATP Carrier Required for Medium-Chain Fatty Acid β-Oxidation and Normal Peroxisome Proliferation in Saccharomyces cerevisiae

Por van Roermund, Carlo W. T., Drissen, Roy, van den Berg, Marlene, Ijlst, Lodewijk, Hettema, Ewald H., Tabak, Henk F., Waterham, Hans R., Wanders, Ronald J. A.
Publicado em 2001

An algorithm to predict phenotypic severity in mucopolysaccharidosis type I in the first month of life

Por Kingma, Sandra DK, Langereis, Eveline J, de Klerk, Clasine M, Zoetekouw, Lida, Wagemans, Tom, IJlst, Lodewijk, Wanders, Ronald JA, Wijburg, Frits A, van Vlies, Naomi
Publicado em 2013

N-lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids

Por Jansen, Robert S., Addie, Ruben, Merkx, Remco, Fish, Alexander, Mahakena, Sunny, Bleijerveld, Onno B., Altelaar, Maarten, IJlst, Lodewijk, Wanders, Ronald J., Borst, P., van de Wetering, Koen
Publicado no Proc Natl Acad Sci U S A (2015)

Peroxisomal d-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

Por van Grunsven, Elisabeth G., van Berkel, Emanuel, Ijlst, Lodewijk, Vreken, Peter, de Klerk, Johannis B. C., Adamski, Jerzy, Lemonde, Hugh, Clayton, Peter T., Cuebas, Dean A., Wanders, Ronald J. A.
Publicado em 1998

Role of Isovaleryl-CoA Dehydrogenase and Short Branched-Chain Acyl-CoA Dehydrogenase in the Metabolism of Valproic Acid: Implications for the Branched-Chain Amino Acid Oxidation Pa...

Por Luís, Paula B. M., Ruiter, Jos P. N., IJlst, Lodewijk, Tavares de Almeida, Isabel, Duran, Marinus, Mohsen, Al-Walid, Vockley, Jerry, Wanders, Ronald J. A., Silva, Margarida F. B.
Publicado em 2011

Necrotizing Enterocolitis and Respiratory Distress Syndrome as First Clinical Presentation of Mitochondrial Trifunctional Protein Deficiency

Por Diekman, Eugène F., Boelen, Carolien C. A., Prinsen, Berthil H. C. M. T., IJlst, Lodewijk, Duran, Marinus, de Koning, Tom J., Waterham, Hans R., Wanders, Ronald J. A., Wijburg, Frits A., Visser, Gepke
Publicado em 2012

Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment

Por Bosch, Annet M., Abeling, Nico G. G. M., IJlst, Lodewijk, Knoester, Hennie, van der Pol, W. Ludo, Stroomer, Alida E. M., Wanders, Ronald J., Visser, Gepke, Wijburg, Frits A., Duran, Marinus, Waterham, Hans R.
Publicado em 2010

Mutations in the Gene Encoding 3-Hydroxyisobutyryl-CoA Hydrolase Results in Progressive Infantile Neurodegeneration

Por Loupatty, Ference J., Clayton, Peter T., Ruiter, Jos P. N., Ofman, Rob, IJlst, Lodewijk, Brown, Garry K., Thorburn, David R., Harris, Robert A., Duran, Marinus, DeSousa, Carlos, Krywawych, Steve, Heales, Simon J. R., Wanders, Ronald J. A.
Publicado em 2007